The Cephalopod Loligo bleekeri Mitochondrial Genome: Multiplied Noncoding Regions and Transposition of trna Genes

Save this PDF as:
 WORD  PNG  TXT  JPG

Size: px
Start display at page:

Download "The Cephalopod Loligo bleekeri Mitochondrial Genome: Multiplied Noncoding Regions and Transposition of trna Genes"

Transcription

1 J Mol Evol (2002) 54: DOI: /s Springer-Verlag New York Inc The Cephalopod Loligo bleekeri Mitochondrial Genome: Multiplied Noncoding Regions and Transposition of trna Genes Kozo Tomita, 1,* Shin-ichi Yokobori, 2 Tairo Oshima, 2 Takuya Ueda, 3 Kimitsuna Watanabe 1,3 1 Department of Chemistry and Biotechnology, Graduate School of Engineering, University of Tokyo, Hongo, Bunkyo-ku, Tokyo , Japan 2 Department of Molecular Biology, School of Life Science, Tokyo University of Pharmacy and Life Science, , Horinouchi, Hachioji, Tokyo , Japan 3 Department of Integrated Biosciences, Graduate School of Frontier Sciences, University of Tokyo, Hongo, Bunkyo-ku, Tokyo , Japan Received: 9 May 2001 / Accepted: 3 October 2001 Abstract. We previously reported the sequence of a 9260-bp fragment of mitochondrial (mt) DNA of the cephalopod Loligo bleekeri [J. Sasuga et al. (1999) J. Mol. Evol. 48: ]. To clarify further the characteristics of Loligo mtdna, we have sequenced an 8148-bp fragment to reveal the complete mt genome sequence. Loligo mtdna is 17,211 bp long and possesses a standard set of metazoan mt genes. Its gene arrangement is not identical to any other metazoan mt gene arrangement reported so far. Three of the 19 noncoding regions longer than 10 bp are 515, 507, and 509 bp long, and their sequences are nearly identical, suggesting that multiplication of these noncoding regions occurred in an ancestral Loligo mt genome. Comparison of the gene arrangements of Loligo, Katharina tunicata, and Littorina saxatilis mt genomes revealed that 17 trna genes of the Loligo mt genome are adjacent to noncoding regions. A majority (15 trna genes) of their counterparts is found in two trna gene clusters of the Katharina mt genome. Therefore, the Loligo mt genome (17 trna genes) may have spread over the genome, and this may have been coupled with the multiplication of the noncoding regions. Maximum likelihood analysis of mt protein genes supports the clade Mollusca + Annelida + Brachiopoda but *Present address: Department of Biochemistry, University of Washington, Seattle, WA , USA Correspondence to: Shin-ichi Yokobori; ls.toyaku.ac.jp fails to infer the relationships among Katharina, Loligo, and three gastropod species. Key words: Cephalopod Loligo bleekeri Mitochondrial DNA Molluscan phylogeny Gene rearrangement Noncoding region trna Introduction Typical metazoan mitochondrial (mt) genomes are circular, are kb in size, and encode 13 protein, 2 rrna [small and large subunit rrnas (rrns and rrnl)], and 22 trna (trna, trnc, etc.) genes but no introns (Wolstenholme 1992; Boore 1999). The 13 polypeptides are involved in ATP synthesis coupled with electron transfer during O 2 consumption [ATP synthetase subunits 6 and 8 (atp6 and atp8), cytochrome oxidase subunits I III (cox1 cox3), apocytochrome b (cob), and NADH dehydrogenase subunits 1 6 and 4L (nad1-6 and nad4l)]. Although the mt gene order is well conserved in several phyla (e.g., Arthropoda and Vertebrata), large variations in mt genome structure have been found within and between several specific groups of Mollusca. Complete mtdna sequences have been reported for various mollusks: a polyplacophoran [Katharina tunicata (Boore and Brown 1994)] and three gastropods, Cepaea nemoralis [Pulmonata (Terrett et al. 1996; Yamazaki et al. 1997)], Albinaria coerulea [Pulmonata

2 487 Fig. 1. Amplification strategy of the Loligo mtdna segment sequenced in this study (upper panel) and complete gene organization of the Loligo mtdna (lower panel). The relative position of each PCR fragment is shown by a horizontal bar. Sequences of the PCR primers are listed in the text. The circular genome is shown in a linear form. Genes encoded on the opposite strand are in gray boxes. trna genes are shown using one-letter abbreviations above the panel, or below the panel in the case of those encoded on the opposite strand. trnl(uaa), trnl(uag), trns(uga), and trns(gcu) are designated L 1,L 2,S 1, and S 2, respectively. The noncoding regions (>10 bp) are designated NC1, etc., and shown in black boxes.

3 488 (Hatzoglou et al. 1995)], and Pupa strigosa [Opisthobranchia (Kurabayashi and Ueshima 2000)]. In addition, the complete mtdna gene arrangements of the bivalve Mytilus edulis (Hoffmann et al. 1992; see also Beagley et al. 1999) and a third pulmonate, Euhadra herklotsi (Yamazaki et al. 1997), have been reported. The size of molluscan mtdna is from 14 kb [pulmonate gastropods (e.g., Terrett et al. 1996)] to approximately 34 kb [the scallop Placopecten magellanicus (e.g., La Roche et al. 1990)]. The gene arrangement of Mytilus mtdna is notably different from that of other known metazoan mtdnas in that atp8 is absent and an additional trna Met gene is present (Hoffmann et al. 1992). Katharina, Mytilus, and opisthobranch/pulmonate gastropods exhibit marked differences in their mt gene arrangements (see Kurabayashi and Ueshima 2000), and the pulmonate mt gene orders differ even among species belonging to the same family (Yamazaki et al. 1997; Kurabayashi and Ueshima 2000). For this reason, comparison of mt gene organization has become a popular means of inferring metazoan phylogeny (see Boore 1999). Although Cephalopoda is one of the major classes of Mollusca, no complete mt genome has been sequenced so far. We previously reported a 9240-bp mtdna fragment of the squid Loligo bleekeri (Sasuga et al. 1999) and found that the Loligo mt genome has a gene arrangement different from that of other mollusks such as Katharina. To characterize the cephalopod mt genome, we have sequenced the remaining region of the Loligo mt genome. The Loligo mt genome carries several long noncoding regions, which appear to be related to differences in mt gene arrangement between Loligo and other mollusks. Materials and Methods DNA Preparation, PCR, Cloning, and Sequencing Total DNA was prepared from livers of Loligo by the conventional phenol-extraction method (Sambrook et al. 1989). The region of Loligo mtdna that had not been determined previously was amplified by PCR (Saiki et al. 1988) as seven fragments, using the following primers designed according to the partial sequence of Loligo mtdna (Sasuga et al. 1999; unpublished results): fragment A, 5 -gggaattc TAAATTATTCACATAATTCTGCC-3 and 5 -gggaagcttg- GATCCTTGGTTTCATTCAT-3 ; fragment B, 5 -gggaattc AAATATACAATCATAGCAAGTC-3 and 5 -gggaagcttg- TATATCTTTATTTGATTATGGTT-3 ; fragment C, 5 gggaattcccgtaaaggaccttcac-3 and 5 -gggaagct- TGGGGAATCTGAACTTGTATCT-3 ; fragment D, 5 -TTCTT CGATCCTTTCGTA-3 and 5 -TTTATCAAAAACATCTCTCTTTG- 3 ; fragment E, 5 -gggctgcagacaaactaataaccaatac- CCTTA-3 and 5 -gggctgcagcagaccggcgtgagccag- GTTG-3 ; fragment F, 5 -gggggatccttatgctacctt AGTACAGTTAA-3 and 5 -gggctgcagggttgtaggaata TATAATAATAGATG-3 ; and fragment a, 5 -gggaattcttaac- TATTCTCTTAATTGGCCT-3 and 5 -gggctgcagggtgtttt- TAGTACGCCCCT-3. Underlined letters indicate restriction enzyme sites introduced for the convenience of ligation with the cloning vectors; lowercase letters denote additional 5 sequences inserted to ensure efficient digestion by the restriction enzymes. The relative locations of the PCR fragments are shown in Fig. 1 (upper panel). PCR was carried out as described by Saiki et al. (1988) in 50 L of a solution containing 10 mm Tris Cl, ph 8.4 (at 25 C), 2 mm MgCl 2, 400 M dntps, 25 pmol of each PCR primer, 2.5 U of Taq DNA polymerase, and 150 ng of total Loligo DNA. The mixtures were subjected to 30 cycles of PCR (one cycle: 94, 50 55, and 72 C for 1, 1, and 1.5 min, respectively). PCR-amplified fragments, purified on a QIAgen spin column (Qiagen) according to the manufacturer s protocol, were digested with restriction endonuclease and then ligated to puc18. Escherichia coli JM109 was transformed with the recombinant plasmids. DNA was sequenced using the dideoxy-termination method with Sequenase version 2.0 (Amersham). Synthetic oligonucleotide primers based on the newly obtained sequence were used for sequence extension. More than three independent clones were analyzed for each DNA clone. Data Analysis The nucleotide sequence of Loligo mtdna was analyzed using the GENETYX software package (Software Development Co. Ltd., Tokyo). trna genes were identified by the formation of cloverleaf secondary structures. Clustal X (Thompson et al. 1997) was used to align amino acid sequences inferred from the Loligo mtdna sequence with the counterparts of various metazoans. The complete sequence of Loligo mtdna is available through the DDBJ/EMBL/GenBank DNA databases under accession number AB Phylogenetic Analyses Based on Primary Sequences Amino acid sequences of mt protein genes were subjected to maximum likelihood (ML) analysis. Each protein gene was extracted from the following complete nucleotide sequences retrieved from the GenBank database: Metridium senile (accession number AF000023), Homo sapiens (J01415), Eumeces egregius (AB016606), Cyprinus carpio (X61010), Petromyzon marinus (U11880), Branchiostoma lanceolatum (Y16474), Balanoglossus carnosus (AF051097), Asterina pectinifera (D16387), Florometra serratissima (AF049132), Drosophila yakuba (X03240), D. melanogaster (U37541), Ceratitis capitata (AJ242872), Anopheles gambiae (L20934), A. quadrimaculatus (L04272), Locusta migratoria (X80245), Artemia franciscana (X69067), Daphnia pulex (AF117817), Ixodes hexagonus (AF081828), Rhipicephalus sanguineus (AF081829), Lumbricus terrestris (U24570), Platynereis dumerilii (AF178678), Katharina tunicata (U09810), Albinaria coerulea (X83390), and Terebratulina retusa (AJ245743). A sequence fragment of the gastropod Littorina saxatilis (LSA132137) was also retrieved. Together with the counterparts of the Loligo mt genome, all protein genes of interest were extracted and translated to amino acid sequences. Each protein gene was aligned using Clustal X (Thompson et al. 1997). After the alignments were slightly modified by hand, regions where the alignment was not satisfactory were removed. Two data sets were prepared. One was a combination of atp6, atp8, cox1, cox2, cob, nad1, and nad6 data (1052 sites in total); the other was a combination of all genes (2301 sites in total). The alignments used for the phylogenetic analyses are available from S.Y. on request. The phylogenetic analyses were carried out by the ML method using PROTML in MOLPHY 2.3b (Adachi and Hasegawa 1996). First, the ML distances between all pairs of taxa were estimated by PROTML using the distance (D) option with the mtrev-f model. Then, a neighbor-joining (NJ) tree was reconstructed by NJDIST in MOLPHY. The NJ trees were used as the start topologies for the local rearrangement

4 489 search (R) option of ML trees by PROTML with the mtrev-f model as the substitution model. To compare the substitution rates among molluscan sequences, the 1056-site data prepared for ML analysis were analyzed with RRTree (Robinson-Rechavi and Huchon 2000). Strand-Specific Bias AT skew and GC skew (Perna and Kocher 1995) were calculated at each codon position of protein genes from the Loligo (this study; Sasuga et al. 1999), Katharina (Boore and Brown 1994), Littorina (partial) (Wilding et al. 1999), Pupa (Kurabayashi and Ueshima 2000), Lumbricus (Boore and Brown 1995), and Terebratulina (Stechmann and Schlegel 1999) mt genomes. The genes atp6, atp8, cox3, and nad3 (atp6 and atp8 only for Littorina) were encoded by the same strand in each of the mt genomes listed above. Similarly, cox1, cox2, and nad2 [cox1 (partial) and nad2 for Littorina] were encoded by the same strand, and nad1, nad4l, nad4, nad6, and cob [nad1, nad6, and cob (partial) for Littorina] were also encoded by the same strand. Therefore, we categorized the protein genes into three groups: A, B, and C. For the first and second positions, all the codons except those used for initiation and termination were included in the analyses. For the third position, four degenerate codon boxes were used. The data set sizes (number of codons) were as follows: for Loligo, 664, 1083, and 1972 for groups A, B, and C, respectively; for Katharina, 657, 1076, and 1968; for Littorina, 281, 598, and 690; for Pupa, 647, 1030, and 1909; for Lumbricus, 656, 1072, and 1990; and for Terebratulina, 660, 1067, and The same data set used to analyze the AT skew and GC skew was used to calculate the frequencies of amino acids specified by GT-rich codons (Phe TTY, Leu TTR, Val GTN, Cys TGY, Trp TGR, and Gly GGN) vs those specified by AC-rich codons (Pro CCN, Thr ACN, His CAY, Gln CAR, Lys AAY, and Asn AAR). Results and Discussion Sequence and Gene Content of the Loligo mt Genome Table 1. Amino acid identities (%) of Loligo mt protein genes to those of Katharina, Littorina, Pupa, Terebratulina, and Lumbricus a Gene Katharina Littorina Pupa Terebratulina Lumbricus atp atp cox cox cox cob nad nad nad nad nad4l nad nad a Data are from the following sources: Katharina (Boore and Brown 1994), Littorina (Wilding et al. 1999), Pupa (Kurabayashi and Ueshima 2000), Terebratulina (Stechmann and Schlegel 1999), and Lumbricus (Boore and Brown 1995). The highest identity for each protein gene is indicated by boldface numbers, and the lowest by italic numbers. We newly determined the sequence of an 8148-bp fragment of Loligo mtdna. This sequence, together with that determined previously [9240 bp (Sasuga et al. 1999); there is a 177-bp overlap between these two fragments.], provided the complete sequence of Loligo mtdna, which has a total of 17,211 bp. The nucleotide composition of the complete Loligo mt genome is 38.8% A, 19.4% C, 9.2% G, and 32.5% T (A+T 71.3%, G+T 41.7%, AT skew 0.089, and GC skew 0.358) in the sense strand on which a majority of protein genes is encoded. In the Katharina mt genome, the nucleotide composition of the major coding strand is 31.4% A, 11.9% C, 18.6% G, and 38.1% T (A+T 69.5%, G+T 56.7%, AT skew 0.095, and GC skew 0.199). It was thus confirmed that the ratios of A and T and of G and C in the Loligo and Katharina mt genomes are inverted, as pointed out previously (Sasuga et al. 1999). In the newly sequenced fragment, six protein genes (cox3, nad3, cob, nad6, nadl, and the 5 half of nad2), two rrna genes, and eight trna genes [trnq, trni, trnk, trnp, trns(uga), trns(gcu), trnw, and trnv] were identified. Together with our previous results (Sasuga et al. 1999), Loligo mtdna is concluded to encode a standard set of metazoan mt genes 13 protein, 2 rrna, and 22 trna genes. The complete gene organization of Loligo mtdna is presented in Fig. 1 (lower panel). Protein Genes The genes cox3, cob, nad2, and nad6 start with an ATG codon, nad3 with an ATA codon, and nad1 with an ATT codon. All these protein genes have complete termination codons (TAA or TAG). The sizes of the newly identified Loligo mt protein genes are very similar to those of their counterparts in the Katharina, Littorina, and Pupa mt genomes (data not shown). As shown in Table 1, four of the five Littorina mt protein genes (atp6, atp8, cox2, and nad1) show the highest similarity at the amino acid sequence level to their Loligo counterparts. In the case of nad6, Katharina nad6 has more similarity to its Loligo counterpart than to that of Littorina. With regard to the remaining eight mt protein genes, six Katharina genes and two Lumbricus genes show the highest similarity to their Loligo counterparts. Although Littorina and Pupa belong to Gastropoda, 8 of the 13 Pupa mt protein genes show the lowest similarity to their Loligo counterparts. This suggests that the Pupa mt protein genes might have evolved more rapidly than those of the other species in Table 1 (Loligo, Katharina, Lumbricus, and Terebratulina). The possible evolutionary patterns of these mt protein genes are discussed in more detail later. rrna Genes Loligo mt rrnl and rrns appear to be 1334 and 978 bp long, respectively, which is similar to their Katharina counterparts (Boore and Brown 1994) but longer than

5 490 Fig. 2. Cloverleaf structures of eight Loligo mt trna genes found in the region sequenced in this study (see Fig. 1). those of pulmonate gastropods (e.g., Yamazaki et al. 1997). trna Genes The gene trns(uga) as well as trns(gcu) in the Loligo mt genome can be formed into a cloverleaf structure similar to trns(gcu) of other metazoan mitochondria (Fig. 2). Likewise, mt trns(uga) of Katharina (Boore and Brown 1994), the pulmonates Cepaea and Euhadra (Yamazaki et al. 1997), and the bivalves Mytilus edulis and M. californianus (Beagley et al. 1999) have been reported to lack a D stem, as is the case in nematode mt trns(uga) (Okimoto et al. 1992). However, the pulmonate Albinaria has a D stem in its mt trns(uga) (Hatzoglou et al. 1995); lack of the D stem in this gene is not a common feature among molluscan mt genomes. Loligo trns(uga) has a GG sequence in the D loop and a TTCGA sequence in the T loop; interaction between these two conserved sequences may stabilize the tertiary structure of the trna, as in the cases of typical trnas (Dirheimaer et al. 1995). Only 2 bp can be formed in the D stems of the trnq and trnk (Fig. 2). Three of the eight trna genes [trns(uga), trns(gcu), and trnq] have GG-conserved nucleotides in the D loop. The T stems consist of 5 bp in seven of the trna genes; only trni has a 4-bp T stem. Unlike several trnas in Cepaea and Euhadra mtdnas (Yamazaki et al. 1997), none of the Loligo trna genes have lost their T stem. Metazoan mitochondria use the modified wobble rule, as summarized by Yokobori et al. (2001). While most anticodon sequences of the 22 species of Loligo mt trna genes are sufficient for reading most of the codons according to the mt wobble rule, there are two exceptions related to trnas involved in the translation of nonuniversal genetic codes namely, the AUA codon specifying Met and the AGR codon specifying Ser (see Sasuga et al. 1999). We have found that the C at the anticodon wobble position of Loligo mt trna Met is modified to 5-formylcytidine (f 5 C) (Tomita et al. 1997). This f 5 C nucleotide modification has also been observed in bovine (Moriya et al. 1994), Ascaris (Watanabe et al. 1994), and D. melanogaster (Tomita et al. 1999) mt trnas Met,in which the AUA codon is read as Met. Thus, it is most likely that a modification from C to f 5 C is involved in the recognition of the AUA codon in Loligo mitochondria. We have found that guanosine at the anticodon wobble position of Loligo mt trna Ser GCU is modified to 7-methylguanosine (m 7 G) (Tomita et al. 1998). Modification to m 7 G also occurs at the first anticodon position of mt trna Ser GCU of the starfish Asterias amurensis (Matsuyama et al. 1998). In both cases, all of the AGN codons specify Ser, and it may be that all of the AGN codons are recognized by a single trna species (trna Ser GCU). On the other hand, trna Ser GCU decoding only AGYs has been reported to carry the unmodified G at the first codon position in several metazoans, including bovine (Ueda et al. 1985) and urochordate Halocynthia roretzi mitochondria (Kondow et al. 1999). Thus, it

6 491 is most likely that in Loligo mitochondria, the modification from G to m 7 G is responsible for decoding AGR in addition to AGY codons. Noncoding Region The Loligo mt genome has 19 noncoding regions (NC) (Figs. 1 and 3) longer than 10 bp, 3 of which are longer than 500 bp, namely, NC4 (515 bp), located between trnq and trni; NC8 (507 bp), between trnw and trnk; and NC16 (509 bp), between trng and trna (Fig. 1). These three long NCs have nearly identical sequences (Fig. 3A; the pairwise similarities of NC4/NC8, NC4/ NC16, and NC8/NC16 are 96.5, 97.8, and 95.7%, respectively). Therefore, it is likely that these three NCs originate from a single noncoding region. The differences among the sequences occur mainly at their 5 and 3 ends (Fig. 3A). For instance, NC4 contains (AT) 10 and NC8 contains (AT) 8 (three nucleotides overlap with trnk) at its 3 end (Fig. 3A), whereas NC16 does not contain any (AT) n sequence. In addition to NC4 and NC8, the noncoding regions between trnq and trna (NC10) and between trnl(uag) and cox3 (NC19) contain (AT) 14, and NC19 contains (AT) 12 (two nucleotides overlapping cox3 are included), as reported previously (Sasuga et al. 1999) (Fig. 3B). When the secondary structures of NC4/8/16 were predicted for both strands, several stem-and-loop structures could be formed at the 5 and 3 regions of the strand shown in Fig. 3A (data not shown). In the case of the opposite strand also, several large stem-and-loop structures could be formed. In NC4/8/16, the sequence 5 - ATATAACCATCCACACTCACCCTCCATAAAC-3 occurs twice (boxed in Fig. 3A). However, neither sequence was part of any of the stem-and-loop structures predicted for the strand shown in Fig. 3A, and they were at different positions in stem-and-loop structures for the opposite strand (data not shown). When a BLAST search (BLASTN) was performed for NC4/8/16 against the mitochondrial database in NCBI (Altschul et al. 1997), there were three regions that matched other mt sequences. Sequences similar to the central region (5 -ATAAACAAATAAATAAATA- CATAATA-3 ; underlined in Fig. 3A) were found in the noncoding regions of various mt genomes, such as that of Saccharomyces cerveciae (Foury et al. 1998) (data not shown). For the 5 and 3 regions, several hits were obtained, most of which were noncoding regions. However, no molluscan mtdna sequences hit the NC4 sequence. From these results, it is difficult to visualize the significance of the similarities between the NC4 sequence and other mtdna sequences. It may be that the noncoding sequences determined and the predicted possible secondary structures play some role(s) in the early stages of the replication and transcription process. However, further experiments are needed to clarify this speculation. Phylogenetic Analyses Based on Primary Sequences When combined data on the inferred amino acid sequences of the 13 mt protein genes are used for the ML analysis (Adachi and Hasegawa 1996), Loligo forms a group with Katharina (Fig. 4A). However, the local bootstrap probability (LBP) support for the group is only 62%. In addition, the position of gastropods (Albinaria and Pupa) is far from that of Loligo/Katharina in the ML tree. Quartet puzzling (QP) analysis (Strimmer and von Haeseler 1996), which permits rate variation among sites, did no resolve the relationship among the Loligo/ Katharina group, gastropods (Albinaria and Pupa), annelids (Lumbricus and Platynereis), and a brachiopod (Terebratulina) (data not shown). When the gastropod Littorina (1052 residues) is included in the ML analysis, Littorina and Katharina form a group (Fig. 4B) with an LBP of 83%. In the ML tree and the QP tree (data not shown), the relationship among Katharina/Littorina, Loligo, and Terebratulina is not resolved. In addition, the gastropods (Littorina, Albinaria, and Pupa) do not form a monophyletic group in these trees. These results are essentially the same as those of Stechmann and Schlegel (1999), in which cephalopod data are not included. Thus, the monophyly of Mollusca (Polyplacophora, Gastropoda, and Cephalopoda in these analyses) as well as the phylogenetic position of Cephalopoda within Mollusca could not be satisfied, as was the case with 18S rrna analyses (e.g., Winnepenninckx et al. 1996), although the monophyly of Mollusca is widely accepted from morphological studies (e.g., Nielsen 1995; Willmer 1990). A close relationship among Annelida, Brachiopoda, and Mollusca has been suggested by 18S rrna analysis (e.g., Cohen 2000). A close relationship between Annelida and Mollusca has also been suggested by analysis of partial elongation factor 1 (EF-1 ) sequences (Kojima et al. 1993), as well as 18S rrna analyses (e.g., Aguinaldo et al. 1997). In addition, an Annelida Mollusca grouping rather than an Annelida Arthropoda grouping has been suggested by various analyses, based not only on molecular phylogenetics but also on morphological studies (e.g., Eernisse et al. 1992). Why is the monophyly of Mollusca not supported in the above analyses, even though the monophyletic origin of Mollusca is widely accepted (e.g., Nielsen 1995; Willmer 1990)? As noted earlier, either Katharina or Littorina protein genes exhibit the highest similarity to their Loligo counterparts except for cox3 and nad3; in these two cases, the Lumbricus genes show the highest similarity. Eight of the 13 Pupa mt protein genes have

7 492 Fig. 3. Comparison of the long noncoding sequences in Loligo mtdna. A NC4, NC8, and NC16. Each location is shown in Fig. 1. Positions where the three noncoding sequences have the same nucleotide are denoted by asterisks. Repeated regions are boxed. The sequence 5 -ATAAACAAATAAATAAATACATAATA-3 mentioned in the text is underlined. B Noncoding sequences other than NC4, NC8, and NC16. For positions of noncoding regions, see Fig. 1.

8 493 Fig. 4. ML trees of protostomes based on the inferred amino acid sequences of mt protein genes. A Without Littorina. B With Littorina. See Materials and Methods for details. the lowest identity among the species compared in Table 1. Such heterogeny of the rate of evolution among molluscan mt genome sequences might have led to the construction of an incorrect tree; the Albinaria and Pupa sequences might have evolved more rapidly than the Katharina, Loligo, and Littorina sequences (Fig. 4). To address this issue, the aligned sequence data used for the ML analysis presented in Fig. 4B were used for a relative rate test (Robinson-Rechavi and Huchon 2000). When D. yakuba is treated as the outgroup, there are no significant differences in the substitution rates among the molluscan species (data not shown). However, D. yakuba may be too distal an outgroup for this analysis. If the monophyly of Mollusca is accepted, although the ML trees in Fig. 4 do not support this, Annelida might be a much better outgroup for Mollusca than D. yakuba. When the annelid species (Lumbricus and Platynereis) are used as the outgroup, Albinaria apparently shows a significantly higher substitution rate than Katharina (p << 0.01, where the null hypothesis is that the two species compared show the same substitution rate), Loligo (p << 0.01), and Littorina (p 0.010). In addition, Pupa also exhibits a significantly higher substitution rate than Katharina (p 0.043) and Littorina (p 0.014), although the difference in substitution rates between Pupa and Loligo is not significant (p 0.232). Thus, the substitution rates of the molluscan species compared here vary, the rates of Pupa and Albinaria being higher than those of the other mollusks. This could affect the shape of the recovered phylogenetic trees. Another factor, related to the tempo of evolutionary change, which could have led to the construction of an

9 494 incorrect tree is the differences in nucleotide composition among molluscan and other protostome mt genes. The second position of a codon is the most conserved of the three codon positions, since changing the nucleotide at the second position changes the property of the encoded amino acid. Although AT and GC skews are in most cases negative at the second codon position, the GC skew of Katharina in groups A (consisting of atp6, atp8, cox3, and nad3) and B (consisting of cox1 and cox2, and nad2) and the GC skew of Loligo in group C (consisting of nad1, nad4 nad6, and nad4l) are positive (Fig. 5A). The AT skews of Katharina at the first and third positions of the codons in groups A and B are negative as in the cases of the second codon positions, and the GC skews are positive as in the cases of the second codon positions. For the same gene sets (groups A and B), the AT skew is very small and the GC skew is negative at the first and third positions of Loligo codons. On the other hand, in the case of group C the AT skew is very small and GC skew is negative at the first and third positions of Katharina codons, but the AT skews of Loligo at the first and third positions of the codons in the groups are negative as in the cases of the second codon positions, and the GC skews are positive as in the cases of the second codon positions. Thus, it can be concluded that the AT and GC skews are inverted, which means that the bias is inverted, between the same genes of Loligo and Katharina. The different direction of bias found in Loligo and Katharina mt protein genes affects the amino acid composition of the resultant polypeptides (Fig. 5B). The frequencies of GT amino acids (those encoded by GGN, GTN, TGN, and TTN codons) and AC amino acids (those encoded by AAN, ACN, CAN, and CCN codons) are very different between groups A/B and group C in the Loligo and Katharina mt genomes, respectively. Furthermore, the bias of GT-amino acid richness/shortness and that of AC-amino acid richness/shortness are opposite if they are compared between the counterparts of the Loligo and Katharina mt genomes. Thus, nucleotide usage in Katharina and Loligo mt protein genes is governed not only by the gene type but also by another constraint. This is most likely to be strand-specific directional mutation pressure (Asakawa et al. 1991) operating on the genes. All three codon positions appear to have been affected by this directional mutation pressure, which would have given rise to the different amino acid compositions of the Loligo and Katharina mt protein genes. All the mt protein genes in Littorina, Terebratulina, and Lumbricus are encoded by a single strand; hence the AC/GT bias of these genomes is likely to change the nucleotide and amino acid compositions in same direction for all the genes (Figs. 5A and B). On the other hand, the AC/GT bias is not an apparent constraint of amino acid usage in the cases of the Pupa mt protein genes (Figs. 5A and B). The branching orders of vertebrate species in the ML trees presented in Fig. 4 differ from the widely accepted view. An unusual branching order of vertebrate species in phylogenetic analysis using mt sequences has been noted when lampreys and nonvertebrate metazoan species, such as echinoderms, are included (e.g., Takezaki and Gojobori 1999). This might be also affected, in part, by differences in amino acid composition between vertebrates and other species (see Takezaki and Gojobori 1999), as postulated for molluscan species (see above). Evolution of Loligo mt Gene Arrangement If only protein and rrna genes are considered, only one inversion event would explain the difference in the mt gene order between Katharina and the brachiopod Terebratulina, which appears as a species very closely related to mollusks in the phylogenetic tree based on mt protein gene sequences, as discussed above (Fig. 6). Similarly, the difference in protein/rrna mt gene arrangement between Katharina and Littorina (reported region) is explained by one inversion (Fig. 6). On the other hand, the difference in the arrangement between the Katharina and the Loligo mt genomes is a more complex issue, since five gene blocks are recognized and are arranged in different orders in the Loligo and Katharina mt genomes (Fig. 6). Two transpositions and one inversion are necessary to explain the difference in gene organization between the Loligo and the Littorina mt genomes (Fig. 6). On the other hand, rearrangement of five gene blocks and two inversions are necessary to explain the difference in gene organization between the Loligo and the Terebratulina mt genomes (Fig. 6). These findings suggest that the Loligo mt genome has a highly scrambled gene arrangement compared with those of the Katharina, Littorina, and Terebratulina mt genomes. trna genes are known to transpose more frequently than protein and rrna genes in metazoan mt genomes (e.g., Pääbo et al. 1991). In addition, trna genes are often found at the end of the deleted/duplicated region, suggesting that they may be hot spots for gene rearrangement events (e.g., Stanton et al. 1994). When trna genes are also included in a comparison of the gene arrangements, the locations of 7 of the 22 trna genes in the Loligo mt genome can be directly compared with the locations of their counterparts in Katharina (Boore and Brown 1994) and Littorina (Wilding et al. 1999) (Fig. 7A). (Genes encoded by the opposite strand are underlined.) The order, rrns trnv rrnl, is shared by these mt genomes as well as by various nonmolluscan mt genomes (i.e., most vertebrate and arthropod mt genomes, as well as annelid and Terebratulina mt genomes). The Loligo mt genome shares the orders trns(gcu) nad2, trnt nad4l, nad5 trnf, and cob trns(uga) with the Katharina mt genome (regions containing these genes are not known for Littorina); these orders are also found in

10 495 Fig. 5. A Comparison of AT skew and GC skew (Perna and Kocher 1995) among three codon positions, among three groups, and among the Loligo (this study; Sasuga et al. 1999), Katharina (Boore and Brown 1994), Littorina [partial (Wilding et al. 1999)], Pupa (Kurabayashi and Ueshima 2000), Lumbricus (Boore and Brown 1995), and Terebratulina (Stechmann and Schlegel 1999) mt genomes. The mt protein genes are divided into three groups (A, B, and C). Black and White bars indicate AT skews and GC skews, respectively. For details, see Materials and Methods. B Comparison of frequencies of GT amino acids and AC amino acids among Loligo, Katharina, Littorina (partial), Pupa, Lumbricus, and Terebratulina. The same data set as that for A was used for analysis. Black and white bars indicate the appearance percentages of the GT amino acids and the AC amino acids, respectively.

11 496 Fig. 6. Comparison of the arrangement of rrna and protein genes among the Loligo, Katharina (Boore and Brown 1994), Littorina (Wilding et al. 1999), and Terebratulina (Stechmann and Schlegel 1999) mt genomes. Genes encoded on the opposite strand are shown in gray boxes.

12 497 Fig. 7. A Comparison of gene arrangement among the Loligo, Katharina (Boore and Brown 1994), and Littorina (Wilding et al. 1999) mt genomes. The conserved gene orders (at least, the order of the gene pair) between two genomes are indicated by bars. 4L, nad4l. Genes encoded on the opposite strand are shown in gray boxes. B Comparison of the partial orders of noncoding regions and flanking trna genes in the Loligo mt genome and those of the and trna gene clusters (see text), trnl(uaa), trnl(uag), and trnh in the Katharina mt genome (Boore and Brown 1994). Lengths of noncoding regions (NC4, etc.) are shown.

13 498 most arthropod mt genomes [trns(gcu) nad2, trnt nad4l, nad5 trnf, and cob trns(uga)], annelid mt genomes [trns(gcu) nad2 and nad5 trnf], and the Terebratulina mt genome [trns(gcu) nad2 and nad5 trnf]. Therefore, these orders might be ancestral features of molluscan mtdna. The Loligo and Littorina mt genomes share the positions of two trna genes, trnd atp8 and trnp nad6, which are not shared by the Katharina mt genome (Fig. 7A). The order trnd atp8 is also found in the Lumbricus (Boore and Brown 1995) and Terebratulina (Stechmann and Schlegel 1999) mt genomes as well in as most arthropod mt genomes. This suggests that the order trnd atp8 might be the ancestral gene order for molluscan mt genomes. On the other hand, the direction of trnp in the Katharina mt genome (trnp nad6) is inverted in relation to that in the Loligo and Littorina mt genomes (trnp nad6) (Fig. 7A). The arthropod (such as Drosophila) mt genome has the order trnp nad6 (Clary and Wolstenholme 1985), which is similar to the case for the Katharina mt genome. Therefore, the order trnp nad6 found in the Loligo and Littorina mt genomes may be a synapomorphic trait and may be derived from the order trnp nad6 found in the Katharina and Drosophila mt genomes. It is notable that the order trnp nad6 is found in the opisthobranch gastropod Pupa mt genome (Kurabayashi and Ueshima 2000), whose gene arrangement is much different from those of other molluscan mt genomes. trna Genes Flanking Noncoding Regions in the Loligo mt Genome Fifteen of 22 trna genes in the Loligo mt genome are positioned differently from their counterparts in the Katharina/Littorina mt genomes. Twelve of these 15 Loligo mt trna genes are found in two trna gene clusters in the Katharina mt genome (Fig. 7B). One of these is the cluster between rrns and cox3 (trnm trnc trny trnw trnq trng trne) (hereafter referred to as the cluster); the other is between cox3 and nad3 (trnk trna trnr trnn trni) (referred to as the cluster) (Boore and Brown 1994). A short (141-bp long) noncoding region is found between trne and cox3 in the Katharina mt genome, containing an AT stretch (34 repeats of TA dinucleotides) (Boore and Brown 1994). As shown in Fig. 7B, one of the ends of the noncoding regions NC4, NC8, NC10, and NC12 is flanked by the trna gene found in the cluster, and the other is flanked by the trna gene found in the cluster. Furthermore, the relative directions of the trna gene originating from the cluster and that originating from the cluster are the same as the original relative directions of the and the clusters. Because they are highly similar, NC4, NC8, and NC16 are likely to have originated from a single noncoding region. Hence, multiplication of the noncoding regions would correlate with the transposition of the trna genes flanking them (discussed later). The genes trnl(uaa) and trnl(uag), located between nad1 and rrnl in the Katharina and Littorina mt genomes, are replaced by the block NC3 trnq NC4 trni NC5 in the Loligo mt genome (Figs. 7A and B). trnl (uaa) is located downstream of trng (Figs. 7A and B), and trnl(uag) flanks NC19 together with trnh (Figs. 7A and B), as reported previously (Sasuga et al. 1999). As noted above, the Katharina mt gene arrangement might retain more ancestral features than the Loligo mt gene arrangement (see Fig. 6). Let us consider that the order trnm trnc trny trnw trnq trng trne NC cox3 trnk trna trnr trnn trni in the Katharina mt genome was rearranged to trnm trnc trny trnw trnq trng trne NC trnk trna trnr trnn trni cox3 in the ancestral Loligo mt genome. If this were the case, the noncoding region might be the ancestor of NC4, NC8, and NC16 of the Loligo mt genome as well as of other shorter noncoding regions (NC10, NC12, and probably NC19). Sequential multiplication of the noncoding region with the flanking trna gene clusters might have occurred in the ancestral Loligo mt genome. After or during multiplication of the noncoding regions with the flanking trna genes, loss of some trna genes in each copy might have occurred and trna Leu genes might have been transposed with the set of the noncoding region and the flanking trna genes after insertion of the ancestral NC4 and its flanking trna genes near the trna Leu genes between nad1 and rrnl. trna genes have been considered as hot spots located at the ends of duplicated fragments in various mt genomes (e.g., Stanton et al. 1994). In addition, the frequent occurrence of gene rearrangement around noncoding regions that contain the origins and/or regulation elements for replication and/or transcription has been found in various mt genomes (e.g., Zevering et al. 1991). Among the six long noncoding regions with flanking trna genes (NC4, -8, -10, -12, -16, and -19), four (NC8, -12, -16, and -19) are located at the junctions of blocks for protein and rrna genes conserved between the Loligo and the Katharina mt genomes. This suggests that the rearrangement of gene blocks mentioned in Fig. 6 might somehow correlate with the spread of noncoding regions. NC4 with flanking trnq and trni is located downstream of rrnl. In vertebrate mt genomes, trnl(uaa) located downstream of rrnl is known to contain an element for the termination of transcription, so that more rrnas than mrnas are transcribed (Attardi 1985). Therefore, the region trnq NC4 trni may play the same role. Alternatively, if both NC4 and NC8 contain initiation points for transcription, and those in NC4 are controlled differently than those in NC8, control of amounts of rrna transcripts relative to those of mrnas (an excess of rrnas) would be realized. Because of the high degrees of similarity among NC4, NC8, and NC16, some stages in the multiplication of the

14 499 noncoding regions and cotranslocations of flanking trna genes are considered not to be ancient events. Alternatively, the concerted evolution of these noncoding regions may have maintained the identity of their primary sequences, as proposed for the two nearidentical noncoding regions of the Dinodon mt genome by Kumazawa et al. (1998). Homologous recombination between mtdna molecules (Thyagarajan et al. 1996) is also a possible mechanism for retention of sequence identity among these noncoding regions. Analysis of other squid and cuttlefish mt genomes might help enlighten our understanding of the evolution of the Loligo bleekeri mt genome structure and might reveal the usefulness of the mt genome structure for elucidating cephalopod phylogeny. Acknowledgments. This work was supported by a Grant-in-Aid for Scientific Research on Priority Areas from the Ministry of Education, Culture, Sports, Science and Technology of Japan to K.W., a grant from the Human Frontier Science Program Organization to K.W., and grants from the Ministry of Education, Culture, Sports, Science and Technology of Japan to T.O. and S.Y. References Adachi J, Hasegawa M (1996) MOLPHY 2.3b. Institute of Statistical Mathematics, Tokyo Aguinaldo AM, Turbeville JM, Linford LS, Rivera MC, Garey JR, Raff RA, Lake JA (1997) Evidence for a clade of nematodes, arthropods and other moulting animals. Nature 387: Altschul SF, Madden TL, Schäffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ (1997) Gapped BLAST and PSI-BLAST: A new generation of protein database search programs. Nucleic Acids Res 25: Asakawa S, Kumazawa Y, Araki T, Himeno H, Miura K, Watanabe K (1991) Strand-specific nucleotide composition bias in echinoderm and vertebrate mitochondrial genomes. J Mol Evol 32: Attardi G (1985) Animal mitochondrial DNA: An extreme example of genetic economy. Int Rev Cytol 93: Beagley CT, Okimoto R, Wolstenholme DR (1999) Mytilus mitochondrial DNA contains a functional gene for a trna Ser UCN with a dihydrouridine arm-replacement loop and a pseudo-trna Ser UCN gene. Genetics 152: Boore JL (1999) Animal mitochondrial genomes. Nucleic Acids Res 27: Boore JL, Brown WM (1994) Complete DNA sequence of the mitochondrial genome of the black chiton, Katharina tunicata. Genetics 138: Boore JL, Brown WM (1995) Complete sequence of the mitochondrial DNA of the annelid worm Lumbricus terrestris. Genetics 141: Clary DO, Wolstenholme DR (1985) The mitochondrial DNA molecular of Drosophila yakuba: Nucleotide sequence, gene organization, and genetic code. J Mol Evol 22: Cohen BL (2000) Monophyly of brachiopods and phoronids: Reconciliation of molecular evidence with Linnaean classification (the subphylum Phoroniformea nov.). Proc R Soc Lond B Biol Sci 267: Dirheimaer G, Keith G, Dumas P, Westhof E (1995). Primary, secondary, and tertiary structures of trnas. In: Söll D, RajBahandary UL (eds) trna: Structure, biosynthesis and function. ASM Press, Washington, DC, pp Eernisse DJ, Albert JS, Anderson FE (1992) Annelida and Arthropoda are not sister taxa: A phylogenetic analysis of spiralian metazoan morphology. Syst Biol 41: Foury F, Roganti T, Lecrenier N, Purnelle B (1998) The complete sequence of the mitochondrial genome of Saccharomyces cerevisiae. FEBS Lett 440: Hatzoglou E, Rodakis GC, Lecanidou R (1995) Complete sequence and gene organization of the mitochondrial genome of the land snail Albinaria coerulea. Genetics 140: Hoffmann RJ, Boore JL, Brown WM (1992) A novel mitochondrial genome organization for the blue mussel, Mytilus edulis. Genetics 131: Kojima S, Hashimoto T, Hasegawa M, Murata S, Ohta S, Seki H, Okada N (1993) Close phylogenetic relationship between Vestimentifera (tube worms) and Annelida revealed by the amino acid sequence of elongation factor-1. J Mol Evol 37:66 70 Kondow A, Suzuki T, Yokobori S, Ueda T, Watanabe K (1999) An extra trna Gly U*CU found in ascidian mitochondria responsible for decoding non-universal codons AGA/AGG as glycine. Nucleic Acids Res 27: Kumazawa Y, Ota H, Nishida M, Ozawa T (1998) The complete nucleotide sequence of a snake (Dinodon semicarinatus) mitochondrial genome with two identical control regions. Genetics 150: Kurabayashi A, Ueshima R (2000) Complete sequence of the mitochondrial DNA of the primitive opisthobranch gastropod Pupa strigosa: Systematic implication of the genome organization. Mol Biol Evol 17: La Roche J, Snyder M, Cook DI, Fuller K, Zouros E (1990) Molecular characterization of a repeat element causing large-scale size variation in the mitochondrial DNA of the sea scallop Placopecten magellanicus. Mol Biol Evol 7: Matsuyama S, Ueda T, Crain PF, McCloskey JA, Watanabe K (1998) A novel wobble rule found in starfish mitochondria. Presence of 7-methylguanosine at the anticodon wobble position expands decoding capability of trna. J Biol Chem 273: Moriya J, Yokogawa T, Wakita K, Ueda T, Nishikawa K, Crain PF, Hashizume T, Pomerantz SC, McCloskey JA, Kawai G, Hayashi N, Yokoyama S, Watanabe, K (1994) A novel modified nucleoside found at the first position of the anticodon of methionine trna from bovine liver mitochondria. Biochemistry 33: Nielsen C (1995) Animal evolution: Interrelationships of the living phyla. Oxford University Press, Oxford Okimoto R, Macfarlane JL, Clary DO, Wolstenholme DR (1992) The mitochondrial genomes of two nematodes, Caenorhabditis elegans and Ascaris suum. Genetics 130: Pääbo S, Thomas WK, Whitfield KM, Kumazawa Y, Wilson AC (1991) Rearrangements of mitochondrial transfer RNA genes in marsupials. J Mol Evol 33: Perna NT, Kocher TD (1995) Patterns of nucleotide composition at fourfold degenerate sites of animal mitochondrial genomes. J Mol Evol 41: Robinson-Rechavi M, Huchon D (2000) RRTree: relative rate tests between groups of sequences on a phylogenetic tree. Bioinformatics 16: Saiki RK, Gelfand DH, Stoffel S, Scharf SJ, Higuchi R, Horn GT, Mullis KB, Erlich HA (1988) Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 239: Sambrook J, Fritsch EF, Maniatis T (1989). Molecular cloning: A laboratory manual, 2nd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY Sasuga J, Yokobori S, Kaifu M, Ueda T, Nishikawa K, Watanabe K (1999) Gene contents and organization of a mitochondrial DNA segment of the squid Loligo bleekeri. J Mol Evol 48: Stanton DJ, Daehler LL, Moritz CC, Brown WM (1994) Sequences with the potential to form stem-and-loop structures are associated with coding-region duplications in animal mitochondrial DNA. Genetics 137:

15 500 Stechmann A, Schlegel M (1999) Analysis of the complete mitochondrial DNA sequence of the brachiopod Terebratulina retusa places Brachiopoda within the protostomes. Proc R Soc Lond B Biol Sci 266: Strimmer K, von Haeseler A (1996) Quartet puzzling: A quartet maximum likelihood method for reconstructing tree topologies. Mol Biol Evol 13: Takezaki N, Gojobori T (1999) Correct and incorrect vertebrate phylogenies obtained by the entire mitochondrial DNA sequences. Mol Biol Evol 16: Terrett JA, Miles S, Thomas RH (1996) Complete DNA sequence of the mitochondrial genome of Cepaea nemoralis (Gastropoda: Pulmonata). J Mol Evol 42: Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG (1997) The CLUSTAL_X windows interface: Flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 25: Thyagarajan B, Padua RA, Campbell C (1996) Mammalian mitochondria possess homologous DNA recombination activity. J Biol Chem 271: Tomita K, Ueda T, Watanabe K (1997) 5-Formylcytidine (f 5 C) found at the wobble position of the anticodon of squid mitochondrial trna Met CAU Nucleic Acids Symp Ser 37: Tomita K, Ueda T, Watanabe K (1998) 7-Methylguanosine at the anticodon wobble position of squid mitochondrial trna Ser GCU: Molecular basis for assignment of AGA/AGG codons as serine in invertebrate mitochondria. Biochim Biophys Acta 1399:78 82 Tomita K, Ueda T, Ishiwa S, Crain PF, McCloskey JA, Watanabe K (1999) Codon reading patterns in Drosophila melanogaster mitochondria based on their trna sequences: A unique wobble rule in animal mitochondria. Nucleic Acids Res 27: Ueda T, Ohta T, Watanabe K (1985) Large scale isolation and some properties of AGY-specific serine trna from bovine heart mitochondria. J Biochem (Tokyo) 98: Watanabe Y, Tsurui H, Ueda T, Furushima R, Takamiya S, Kita K, Nishikawa K, Watanabe K (1994) Primary and higher order structures of nematode (Ascaris suum) mitochondrial trnas lacking either the T or D stem. J Biol Chem 269: Wilding CS, Mill PJ, Grahame J (1999) Partial sequence of the mitochondrial genome of Littorina saxatilis: Relevance to gastropod phylogenetics. J Mol Evol 48: Willmer P (1990) Invertebrate relationships: Patterns in animal evolution. Cambridge University Press, Cambridge Winnepenninckx B, Backeljau T, De Wachter R (1996) Investigation of molluscan phylogeny on the basis of 18S rrna sequences. Mol Biol Evol 13: Wolstenholme DR (1992) Animal mitochondrial DNA: structure and evolution. Int Rev Cytol 141: Yamazaki N, Ueshima R, Terrett JA, Yokobori S, Kaifu M, Segawa R, Kobayashi T, Numachi K, Ueda T, Nishikawa K, Watanabe K, Thomas RH (1997) Evolution of pulmonate gastropod mitochondrial genomes: Comparisons of gene organizations of Euhadra, Cepaea and Albinaria and implications of unusual trna secondary structures. Genetics 145: Yokobori S, Suzuki T, Watanabe K (2001) Genetic code variations in mitochondria: trna as a major determinant of genetic code plasticity. J Mol Evol 53: Zevering CE, Moritz C, Heideman A, Sturm RA (1991) Parallel origins of duplications and the formation of pseudogenes in mitochondrial DNA from parthenogenetic lizards (Heteronotia binoei; Gekkonidae). J Mol Evol 33:

The Complete Mitochondrial Genome of the Articulate Brachiopod Terebratalia transversa

The Complete Mitochondrial Genome of the Articulate Brachiopod Terebratalia transversa The Complete Mitochondrial Genome of the Articulate Brachiopod Terebratalia transversa Kevin G. Helfenbein,* Wesley M. Brown,* and Jeffrey L. Boore* *Department of Biology, University of Michigan, Ann

More information

Partial Sequence of the Mitochondrial Genome of Littorina saxatilis: Relevance to Gastropod Phylogenetics*

Partial Sequence of the Mitochondrial Genome of Littorina saxatilis: Relevance to Gastropod Phylogenetics* J Mol Evol (1999) 48:348 359 Springer-Verlag New York Inc. 1999 Partial Sequence of the Mitochondrial Genome of Littorina saxatilis: Relevance to Gastropod Phylogenetics* Craig S. Wilding, Peter J. Mill,

More information

1. DNA, RNA structure. 2. DNA replication. 3. Transcription, translation

1. DNA, RNA structure. 2. DNA replication. 3. Transcription, translation 1. DNA, RNA structure 2. DNA replication 3. Transcription, translation DNA and RNA are polymers of nucleotides DNA is a nucleic acid, made of long chains of nucleotides Nucleotide Phosphate group Nitrogenous

More information

RNA : functional role

RNA : functional role RNA : functional role Hamad Yaseen, PhD MLS Department, FAHS Hamad.ali@hsc.edu.kw RNA mrna rrna trna 1 From DNA to Protein -Outline- From DNA to RNA From RNA to Protein From DNA to RNA Transcription: Copying

More information

CHAPTER 21 LECTURE SLIDES

CHAPTER 21 LECTURE SLIDES CHAPTER 21 LECTURE SLIDES Prepared by Brenda Leady University of Toledo To run the animations you must be in Slideshow View. Use the buttons on the animation to play, pause, and turn audio/text on or off.

More information

Chapter 13. From DNA to Protein

Chapter 13. From DNA to Protein Chapter 13 From DNA to Protein Proteins All proteins consist of polypeptide chains A linear sequence of amino acids Each chain corresponds to the nucleotide base sequenceof a gene The Path From Genes to

More information

8/21/2014. From Gene to Protein

8/21/2014. From Gene to Protein From Gene to Protein Chapter 17 Objectives Describe the contributions made by Garrod, Beadle, and Tatum to our understanding of the relationship between genes and enzymes Briefly explain how information

More information

Nucleic acids deoxyribonucleic acid (DNA) ribonucleic acid (RNA) nucleotide

Nucleic acids deoxyribonucleic acid (DNA) ribonucleic acid (RNA) nucleotide Nucleic Acids Nucleic acids are molecules that store information for cellular growth and reproduction There are two types of nucleic acids: - deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) These

More information

Fig Ch 17: From Gene to Protein

Fig Ch 17: From Gene to Protein Fig. 17-1 Ch 17: From Gene to Protein Basic Principles of Transcription and Translation RNA is the intermediate between genes and the proteins for which they code Transcription is the synthesis of RNA

More information

PROTEIN SYNTHESIS. copyright cmassengale

PROTEIN SYNTHESIS. copyright cmassengale PROTEIN SYNTHESIS 1 DNA and Genes 2 Roles of RNA and DNA DNA is the MASTER PLAN RNA is the BLUEPRINT of the Master Plan 3 RNA Differs from DNA RNA has a sugar ribose DNA has a sugar deoxyribose 4 Other

More information

Recombinant DNA Technology

Recombinant DNA Technology History of recombinant DNA technology Recombinant DNA Technology (DNA cloning) Majid Mojarrad Recombinant DNA technology is one of the recent advances in biotechnology, which was developed by two scientists

More information

Mutation Rates and Sequence Changes

Mutation Rates and Sequence Changes s and Sequence Changes part of Fortgeschrittene Methoden in der Bioinformatik Computational EvoDevo University Leipzig Leipzig, WS 2011/12 From Molecular to Population Genetics molecular level substitution

More information

Bio 101 Sample questions: Chapter 10

Bio 101 Sample questions: Chapter 10 Bio 101 Sample questions: Chapter 10 1. Which of the following is NOT needed for DNA replication? A. nucleotides B. ribosomes C. Enzymes (like polymerases) D. DNA E. all of the above are needed 2 The information

More information

Basic Concepts of Human Genetics

Basic Concepts of Human Genetics Basic Concepts of Human Genetics The genetic information of an individual is contained in 23 pairs of chromosomes. Every human cell contains the 23 pair of chromosomes. One pair is called sex chromosomes

More information

Chapter 14 Active Reading Guide From Gene to Protein

Chapter 14 Active Reading Guide From Gene to Protein Name: AP Biology Mr. Croft Chapter 14 Active Reading Guide From Gene to Protein This is going to be a very long journey, but it is crucial to your understanding of biology. Work on this chapter a single

More information

Bio11 Announcements. Ch 21: DNA Biology and Technology. DNA Functions. DNA and RNA Structure. How do DNA and RNA differ? What are genes?

Bio11 Announcements. Ch 21: DNA Biology and Technology. DNA Functions. DNA and RNA Structure. How do DNA and RNA differ? What are genes? Bio11 Announcements TODAY Genetics (review) and quiz (CP #4) Structure and function of DNA Extra credit due today Next week in lab: Case study presentations Following week: Lab Quiz 2 Ch 21: DNA Biology

More information

2012 GENERAL [5 points]

2012 GENERAL [5 points] GENERAL [5 points] 2012 Mark all processes that are part of the 'standard dogma of molecular' [ ] DNA replication [ ] transcription [ ] translation [ ] reverse transposition [ ] DNA restriction [ ] DNA

More information

Protein Synthesis

Protein Synthesis HEBISD Student Expectations: Identify that RNA Is a nucleic acid with a single strand of nucleotides Contains the 5-carbon sugar ribose Contains the nitrogen bases A, G, C and U instead of T. The U is

More information

3 Designing Primers for Site-Directed Mutagenesis

3 Designing Primers for Site-Directed Mutagenesis 3 Designing Primers for Site-Directed Mutagenesis 3.1 Learning Objectives During the next two labs you will learn the basics of site-directed mutagenesis: you will design primers for the mutants you designed

More information

MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.

MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question. Exam Chapter 17 Genes to Proteins Name MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question. The following questions refer to Figure 17.1, a simple metabolic

More information

AP2013-DNAPacket-II. Use the list of choices below for the following questions:

AP2013-DNAPacket-II. Use the list of choices below for the following questions: Class: Date: AP2013-DNAPacket-II Multiple Choice Identify the choice that best completes the statement or answers the question. Use the list of choices below for the following questions: I. helicase II.

More information

DNA Replication and Repair

DNA Replication and Repair DNA Replication and Repair http://hyperphysics.phy-astr.gsu.edu/hbase/organic/imgorg/cendog.gif Overview of DNA Replication SWYK CNs 1, 2, 30 Explain how specific base pairing enables existing DNA strands

More information

BIOLOGY LTF DIAGNOSTIC TEST DNA to PROTEIN & BIOTECHNOLOGY

BIOLOGY LTF DIAGNOSTIC TEST DNA to PROTEIN & BIOTECHNOLOGY Biology Multiple Choice 016074 BIOLOGY LTF DIAGNOSTIC TEST DNA to PROTEIN & BIOTECHNOLOGY Test Code: 016074 Directions: Each of the questions or incomplete statements below is followed by five suggested

More information

Lecture Four. Molecular Approaches I: Nucleic Acids

Lecture Four. Molecular Approaches I: Nucleic Acids Lecture Four. Molecular Approaches I: Nucleic Acids I. Recombinant DNA and Gene Cloning Recombinant DNA is DNA that has been created artificially. DNA from two or more sources is incorporated into a single

More information

Chapter 14: Gene Expression: From Gene to Protein

Chapter 14: Gene Expression: From Gene to Protein Chapter 14: Gene Expression: From Gene to Protein This is going to be a very long journey, but it is crucial to your understanding of biology. Work on this chapter a single concept at a time, and expect

More information

M I C R O B I O L O G Y WITH DISEASES BY TAXONOMY, THIRD EDITION

M I C R O B I O L O G Y WITH DISEASES BY TAXONOMY, THIRD EDITION M I C R O B I O L O G Y WITH DISEASES BY TAXONOMY, THIRD EDITION Chapter 7 Microbial Genetics Lecture prepared by Mindy Miller-Kittrell, University of Tennessee, Knoxville The Structure and Replication

More information

Review of Protein (one or more polypeptide) A polypeptide is a long chain of..

Review of Protein (one or more polypeptide) A polypeptide is a long chain of.. Gene expression Review of Protein (one or more polypeptide) A polypeptide is a long chain of.. In a protein, the sequence of amino acid determines its which determines the protein s A protein with an enzymatic

More information

MODULE 1: INTRODUCTION TO THE GENOME BROWSER: WHAT IS A GENE?

MODULE 1: INTRODUCTION TO THE GENOME BROWSER: WHAT IS A GENE? MODULE 1: INTRODUCTION TO THE GENOME BROWSER: WHAT IS A GENE? Lesson Plan: Title Introduction to the Genome Browser: what is a gene? JOYCE STAMM Objectives Demonstrate basic skills in using the UCSC Genome

More information

BEADLE & TATUM EXPERIMENT

BEADLE & TATUM EXPERIMENT FROM DNA TO PROTEINS: gene expression Chapter 14 LECTURE OBJECTIVES What Is the Evidence that Genes Code for Proteins? How Does Information Flow from Genes to Proteins? How Is the Information Content in

More information

Solutions to Quiz II

Solutions to Quiz II MIT Department of Biology 7.014 Introductory Biology, Spring 2005 Solutions to 7.014 Quiz II Class Average = 79 Median = 82 Grade Range % A 90-100 27 B 75-89 37 C 59 74 25 D 41 58 7 F 0 40 2 Question 1

More information

Chapter 17: From Gene to Protein

Chapter 17: From Gene to Protein Name Period This is going to be a very long journey, but it is crucial to your understanding of biology. Work on this chapter a single concept at a time, and expect to spend at least 6 hours to truly master

More information

Protein Synthesis. OpenStax College

Protein Synthesis. OpenStax College OpenStax-CNX module: m46032 1 Protein Synthesis OpenStax College This work is produced by OpenStax-CNX and licensed under the Creative Commons Attribution License 3.0 By the end of this section, you will

More information

The genetic material

The genetic material Basics of molecular genetics The genetic material 1944: Avery, MacLeod & McCarty DNA is the genetic material 1953: Watson & Crick molecular model of DNA structure The genetic material 1977: Maxam & Gilbert

More information

Chapter 8: DNA and RNA

Chapter 8: DNA and RNA Chapter 8: DNA and RNA Lecture Outline Enger, E. D., Ross, F. C., & Bailey, D. B. (2012). Concepts in biology (14th ed.). New York: McGraw- Hill. 1 8-1 DNA and the Importance of Proteins Proteins play

More information

Chapter 10 - Molecular Biology of the Gene

Chapter 10 - Molecular Biology of the Gene Bio 100 - Molecular Genetics 1 A. Bacterial Transformation Chapter 10 - Molecular Biology of the Gene Researchers found that they could transfer an inherited characteristic (e.g. the ability to cause pneumonia),

More information

Protein Synthesis. Application Based Questions

Protein Synthesis. Application Based Questions Protein Synthesis Application Based Questions MRNA Triplet Codons Note: Logic behind the single letter abbreviations can be found at: http://www.biology.arizona.edu/biochemistry/problem_sets/aa/dayhoff.html

More information

Chapter 2 - DNA MC [37 marks]

Chapter 2 - DNA MC [37 marks] Chapter 2 - N MC [37 marks] 1. The image shows a N nucleotide. Which correctly identifies the parts labelled I and II? C 2. Which model represents transcription? 3. Which sequence represents the order

More information

Sequence Analysis Lab Protocol

Sequence Analysis Lab Protocol Sequence Analysis Lab Protocol You will need this handout of instructions The sequence of your plasmid from the ABI The Accession number for Lambda DNA J02459 The Accession number for puc 18 is L09136

More information

CHAPTER 17 FROM GENE TO PROTEIN. Section C: The Synthesis of Protein

CHAPTER 17 FROM GENE TO PROTEIN. Section C: The Synthesis of Protein CHAPTER 17 FROM GENE TO PROTEIN Section C: The Synthesis of Protein 1. Translation is the RNA-directed synthesis of a polypeptide: a closer look 2. Signal peptides target some eukaryotic polypeptides to

More information

Protein Synthesis Notes

Protein Synthesis Notes Protein Synthesis Notes Protein Synthesis: Overview Transcription: synthesis of mrna under the direction of DNA. Translation: actual synthesis of a polypeptide under the direction of mrna. Transcription

More information

CHAPTER 9 DNA Technologies

CHAPTER 9 DNA Technologies CHAPTER 9 DNA Technologies Recombinant DNA Artificially created DNA that combines sequences that do not occur together in the nature Basis of much of the modern molecular biology Molecular cloning of genes

More information

Protein Synthesis & Gene Expression

Protein Synthesis & Gene Expression DNA provides the instructions for how to build proteins Each gene dictates how to build a single protein in prokaryotes The sequence of nucleotides (AGCT) in DNA dictates the order of amino acids that

More information

LECTURE 26. a) A light-independent repair mechanism that involves three steps:

LECTURE 26. a) A light-independent repair mechanism that involves three steps: LECTURE 26 DNA REPAIR A. The capability for repair of damaged DNA is found in one form or another in all organisms. Prokaryotes (e.g., E. coli) have five repair systems, whereas higher organisms (e.g.,

More information

14 Gene Expression: From Gene to Protein

14 Gene Expression: From Gene to Protein CMPBELL BIOLOY IN FOCS rry Cain Wasserman Minorsky Jackson Reece 14 ene Expression: From ene to Protein Lecture Presentations by Kathleen Fitzpatrick and Nicole Tunbridge Overview: The Flow of enetic Information

More information

Genetics Lecture 21 Recombinant DNA

Genetics Lecture 21 Recombinant DNA Genetics Lecture 21 Recombinant DNA Recombinant DNA In 1971, a paper published by Kathleen Danna and Daniel Nathans marked the beginning of the recombinant DNA era. The paper described the isolation of

More information

Multiple choice questions (numbers in brackets indicate the number of correct answers)

Multiple choice questions (numbers in brackets indicate the number of correct answers) 1 Multiple choice questions (numbers in brackets indicate the number of correct answers) February 1, 2013 1. Ribose is found in Nucleic acids Proteins Lipids RNA DNA (2) 2. Most RNA in cells is transfer

More information

Higher Human Biology Unit 1: Human Cells Pupils Learning Outcomes

Higher Human Biology Unit 1: Human Cells Pupils Learning Outcomes Higher Human Biology Unit 1: Human Cells Pupils Learning Outcomes 1.1 Division and Differentiation in Human Cells I can state that cellular differentiation is the process by which a cell develops more

More information

Genomics and Gene Recognition Genes and Blue Genes

Genomics and Gene Recognition Genes and Blue Genes Genomics and Gene Recognition Genes and Blue Genes November 1, 2004 Prokaryotic Gene Structure prokaryotes are simplest free-living organisms studying prokaryotes can give us a sense what is the minimum

More information

THE GENETIC CODE Figure 1: The genetic code showing the codons and their respective amino acids

THE GENETIC CODE Figure 1: The genetic code showing the codons and their respective amino acids THE GENETIC CODE As DNA is a genetic material, it carries genetic information from cell to cell and from generation to generation. There are only four bases in DNA and twenty amino acids in protein, so

More information

Key Concept Translation converts an mrna message into a polypeptide, or protein.

Key Concept Translation converts an mrna message into a polypeptide, or protein. 8.5 Translation VOBLRY translation codon stop codon start codon anticodon Key oncept Translation converts an mrn message into a polypeptide, or protein. MIN IDES mino acids are coded by mrn base sequences.

More information

Biomolecules: lecture 6

Biomolecules: lecture 6 Biomolecules: lecture 6 - to learn the basics on how DNA serves to make RNA = transcription - to learn how the genetic code instructs protein synthesis - to learn the basics on how proteins are synthesized

More information

Annotating 7G24-63 Justin Richner May 4, Figure 1: Map of my sequence

Annotating 7G24-63 Justin Richner May 4, Figure 1: Map of my sequence Annotating 7G24-63 Justin Richner May 4, 2005 Zfh2 exons Thd1 exons Pur-alpha exons 0 40 kb 8 = 1 kb = LINE, Penelope = DNA/Transib, Transib1 = DINE = Novel Repeat = LTR/PAO, Diver2 I = LTR/Gypsy, Invader

More information

Department. Zoology & Biotechnology QUESTION BANK BIOTECHNOLOGY SEMESTER-V

Department. Zoology & Biotechnology QUESTION BANK BIOTECHNOLOGY SEMESTER-V Department of Zoology & Biotechnology QUESTION BANK BIOTECHNOLOGY SEMESTER-V Unit-1 Genetic Material Different forms of DNA(DNA topology):- B-form, Z-form, D-form; Gene structure-introns,exaons and pseudogenes:

More information

RNA: Transcription and Triplet Code

RNA: Transcription and Triplet Code RNA: Transcription and Triplet Code There are Five Kinds of RNA, All of Which are Templated from DNA. The first type of RNA is trna. The "t" stands for "transfer". This RNA is the RNA that transfers amino

More information

Biotechnology Explorer

Biotechnology Explorer Biotechnology Explorer C. elegans Behavior Kit Bioinformatics Supplement explorer.bio-rad.com Catalog #166-5120EDU This kit contains temperature-sensitive reagents. Open immediately and see individual

More information

MATH 5610, Computational Biology

MATH 5610, Computational Biology MATH 5610, Computational Biology Lecture 2 Intro to Molecular Biology (cont) Stephen Billups University of Colorado at Denver MATH 5610, Computational Biology p.1/24 Announcements Error on syllabus Class

More information

Cat # Box1 Box2. DH5a Competent E. coli cells CCK-20 (20 rxns) 40 µl 40 µl 50 µl x 20 tubes. Choo-Choo Cloning TM Enzyme Mix

Cat # Box1 Box2. DH5a Competent E. coli cells CCK-20 (20 rxns) 40 µl 40 µl 50 µl x 20 tubes. Choo-Choo Cloning TM Enzyme Mix Molecular Cloning Laboratories User Manual Version 3.3 Product name: Choo-Choo Cloning Kits Cat #: CCK-10, CCK-20, CCK-096, CCK-384 Description: Choo-Choo Cloning is a highly efficient directional PCR

More information

DNA makes RNA makes Proteins. The Central Dogma

DNA makes RNA makes Proteins. The Central Dogma DNA makes RNA makes Proteins The Central Dogma TRANSCRIPTION DNA RNA transcript RNA polymerase RNA PROCESSING Exon RNA transcript (pre-mrna) Intron Aminoacyl-tRNA synthetase NUCLEUS CYTOPLASM FORMATION

More information

Bundle 5 Test Review

Bundle 5 Test Review Bundle 5 Test Review DNA vs. RNA DNA Replication Gene Mutations- Protein Synthesis 1. Label the different components and complete the complimentary base pairing. What is this molecule called? _Nucleic

More information

Gene Expression: Transcription

Gene Expression: Transcription Gene Expression: Transcription The majority of genes are expressed as the proteins they encode. The process occurs in two steps: Transcription = DNA RNA Translation = RNA protein Taken together, they make

More information

DNA is the genetic material. DNA structure. Chapter 7: DNA Replication, Transcription & Translation; Mutations & Ames test

DNA is the genetic material. DNA structure. Chapter 7: DNA Replication, Transcription & Translation; Mutations & Ames test DNA is the genetic material Chapter 7: DNA Replication, Transcription & Translation; Mutations & Ames test Dr. Amy Rogers Bio 139 General Microbiology Hereditary information is carried by DNA Griffith/Avery

More information

Some types of Mutagenesis

Some types of Mutagenesis Mutagenesis What Is a Mutation? Genetic information is encoded by the sequence of the nucleotide bases in DNA of the gene. The four nucleotides are: adenine (A), thymine (T), guanine (G), and cytosine

More information

STRUCTURAL BIOLOGY. α/β structures Closed barrels Open twisted sheets Horseshoe folds

STRUCTURAL BIOLOGY. α/β structures Closed barrels Open twisted sheets Horseshoe folds STRUCTURAL BIOLOGY α/β structures Closed barrels Open twisted sheets Horseshoe folds The α/β domains Most frequent domain structures are α/β domains: A central parallel or mixed β sheet Surrounded by α

More information

Zool 3200: Cell Biology Exam 3 3/6/15

Zool 3200: Cell Biology Exam 3 3/6/15 Name: Trask Zool 3200: Cell Biology Exam 3 3/6/15 Answer each of the following questions in the space provided; circle the correct answer or answers for each multiple choice question and circle either

More information

3. human genomics clone genes associated with genetic disorders. 4. many projects generate ordered clones that cover genome

3. human genomics clone genes associated with genetic disorders. 4. many projects generate ordered clones that cover genome Lectures 30 and 31 Genome analysis I. Genome analysis A. two general areas 1. structural 2. functional B. genome projects a status report 1. 1 st sequenced: several viral genomes 2. mitochondria and chloroplasts

More information

Self-test Quiz for Chapter 12 (From DNA to Protein: Genotype to Phenotype)

Self-test Quiz for Chapter 12 (From DNA to Protein: Genotype to Phenotype) Self-test Quiz for Chapter 12 (From DNA to Protein: Genotype to Phenotype) Question#1: One-Gene, One-Polypeptide The figure below shows the results of feeding trials with one auxotroph strain of Neurospora

More information

Mutating Asn-666 to Glu in the O-helix region of the taq DNA polymerase gene

Mutating Asn-666 to Glu in the O-helix region of the taq DNA polymerase gene Research in Pharmaceutical Sciences, April 2010; 5(1): 15-19 Received: Oct 2009 Accepted: Jan 2010 School of Pharmacy & Pharmaceutical Sciences 15 Isfahan University of Medical Sciences Original Article

More information

PUC Vikasana Program- 2012

PUC Vikasana Program- 2012 Chromosome Nucleus DNA PUC Vikasana Program- 2012 Introduction Molecular biology is the study of biology at a molecular level. Macromolecules and the macromolecular mechanisms. Interactions between the

More information

Mutagenesis. Classification of mutation. Spontaneous Base Substitution. Molecular Mutagenesis. Limits to DNA Pol Fidelity.

Mutagenesis. Classification of mutation. Spontaneous Base Substitution. Molecular Mutagenesis. Limits to DNA Pol Fidelity. Mutagenesis 1. Classification of mutation 2. Base Substitution 3. Insertion Deletion 4. s 5. Chromosomal Aberration 6. Repair Mechanisms Classification of mutation 1. Definition heritable change in DNA

More information

Lecture 18. PCR Technology. Growing PCR Industry

Lecture 18. PCR Technology. Growing PCR Industry Lecture 18 PCR Technology Growing PCR Industry Basic PCR, Cloning of PCR product, RT-PCR, RACE, Quantitative PCR, Multiplex PCR, Hot start PCR, Touchdown PCR,PCR sequencing.. How PCR started The DNA duplex

More information

Tracing Your Matrilineal Ancestry: Mitochondrial DNA PCR and Sequencing

Tracing Your Matrilineal Ancestry: Mitochondrial DNA PCR and Sequencing Tracing Your Matrilineal Ancestry: Mitochondrial DNA PCR and Sequencing BABEC s Curriculum Rewrite Curriculum to Align with NGSS Standards NGSS work group Your ideas for incorporating NGSS Feedback from

More information

Prokaryotic Transcription

Prokaryotic Transcription Prokaryotic Transcription Transcription Basics DNA is the genetic material Nucleic acid Capable of self-replication and synthesis of RNA RNA is the middle man Nucleic acid Structure and base sequence are

More information

From Gene to Protein via Transcription and Translation i

From Gene to Protein via Transcription and Translation i How do genes influence our characteristics? From Gene to Protein via Transcription and Translation i A gene is a segment of DNA that provides the instructions for making a protein. Proteins have many different

More information

DNA. KEY CONCEPT DNA structure is the same in all organisms.

DNA. KEY CONCEPT DNA structure is the same in all organisms. KEY CONCEPT DNA structure is the same in all organisms. DNA is composed of four types of nucleotides. DNA is made up of a long chain of nucleotides. Each nucleotide has three parts. a phosphate group a

More information

NEW OUTCOMES IN MUTATION RATES ANALYSIS

NEW OUTCOMES IN MUTATION RATES ANALYSIS NEW OUTCOMES IN MUTATION RATES ANALYSIS Valentina Agoni valentina.agoni@unipv.it The GC-content is very variable in different genome regions and species but although many hypothesis we still do not know

More information

Codon usage and secondary structure of MS2 pfaage RNA. Michael Bulmer. Department of Statistics, 1 South Parks Road, Oxford OX1 3TG, UK

Codon usage and secondary structure of MS2 pfaage RNA. Michael Bulmer. Department of Statistics, 1 South Parks Road, Oxford OX1 3TG, UK volume 17 Number 5 1989 Nucleic Acids Research Codon usage and secondary structure of MS2 pfaage RNA Michael Bulmer Department of Statistics, 1 South Parks Road, Oxford OX1 3TG, UK Received October 20,

More information

Transcription and Translation

Transcription and Translation Biology Name: Morales Date: Period: Transcription and Translation Directions: Read the following and answer the questions in complete sentences. DNA is the molecule of heredity it determines an organism

More information

Student Exploration: RNA and Protein Synthesis Due Wednesday 11/27/13

Student Exploration: RNA and Protein Synthesis Due Wednesday 11/27/13 http://www.explorelearning.com Name: Period : Student Exploration: RNA and Protein Synthesis Due Wednesday 11/27/13 Vocabulary: Define these terms in complete sentences on a separate piece of paper: amino

More information

Synthetic Biology. Sustainable Energy. Therapeutics Industrial Enzymes. Agriculture. Accelerating Discoveries, Expanding Possibilities. Design.

Synthetic Biology. Sustainable Energy. Therapeutics Industrial Enzymes. Agriculture. Accelerating Discoveries, Expanding Possibilities. Design. Synthetic Biology Accelerating Discoveries, Expanding Possibilities Sustainable Energy Therapeutics Industrial Enzymes Agriculture Design Build Generate Solutions to Advance Synthetic Biology Research

More information

O C. 5 th C. 3 rd C. the national health museum

O C. 5 th C. 3 rd C. the national health museum Elements of Molecular Biology Cells Cells is a basic unit of all living organisms. It stores all information to replicate itself Nucleus, chromosomes, genes, All living things are made of cells Prokaryote,

More information

7.2 Protein Synthesis. From DNA to Protein Animation

7.2 Protein Synthesis. From DNA to Protein Animation 7.2 Protein Synthesis From DNA to Protein Animation Proteins Why are proteins so important? They break down your food They build up muscles They send signals through your brain that control your body They

More information

General Biology 1004 Chapter 10 Lecture Handout, Summer 2005 Dr. Frisby

General Biology 1004 Chapter 10 Lecture Handout, Summer 2005 Dr. Frisby Slide 1 CHAPTER 10 Molecular Biology of the Gene PowerPoint Lecture Slides for Essential Biology, Second Edition & Essential Biology with Physiology Presentation prepared by Chris C. Romero Neil Campbell,

More information

Gene Expression Translation U C A G A G

Gene Expression Translation U C A G A G Why? ene Expression Translation How do cells synthesize polypeptides and convert them to functional proteins? The message in your DN of who you are and how your body works is carried out by cells through

More information

DNA Transcription. Visualizing Transcription. The Transcription Process

DNA Transcription. Visualizing Transcription. The Transcription Process DNA Transcription By: Suzanne Clancy, Ph.D. 2008 Nature Education Citation: Clancy, S. (2008) DNA transcription. Nature Education 1(1) If DNA is a book, then how is it read? Learn more about the DNA transcription

More information

DNA. translation. base pairing rules for DNA Replication. thymine. cytosine. amino acids. The building blocks of proteins are?

DNA. translation. base pairing rules for DNA Replication. thymine. cytosine. amino acids. The building blocks of proteins are? 2 strands, has the 5-carbon sugar deoxyribose, and has the nitrogen base Thymine. The actual process of assembling the proteins on the ribosome is called? DNA translation Adenine pairs with Thymine, Thymine

More information

RNA & PROTEIN SYNTHESIS

RNA & PROTEIN SYNTHESIS RNA & PROTEIN SYNTHESIS DNA & RNA Genes are coded DNA instructions that control the production of proteins within the cell. The first step in decoding these genetic messages is to copy part of the nucleotide

More information

RNA and PROTEIN SYNTHESIS. Chapter 13

RNA and PROTEIN SYNTHESIS. Chapter 13 RNA and PROTEIN SYNTHESIS Chapter 13 DNA Double stranded Thymine Sugar is RNA Single stranded Uracil Sugar is Ribose Deoxyribose Types of RNA 1. Messenger RNA (mrna) Carries copies of instructions from

More information

Finishing Drosophila Ananassae Fosmid 2728G16

Finishing Drosophila Ananassae Fosmid 2728G16 Finishing Drosophila Ananassae Fosmid 2728G16 Kyle Jung March 8, 2013 Bio434W Professor Elgin Page 1 Abstract For my finishing project, I chose to finish fosmid 2728G16. This fosmid carries a segment of

More information

CHAPTER 20 DNA TECHNOLOGY AND GENOMICS. Section A: DNA Cloning

CHAPTER 20 DNA TECHNOLOGY AND GENOMICS. Section A: DNA Cloning Section A: DNA Cloning 1. DNA technology makes it possible to clone genes for basic research and commercial applications: an overview 2. Restriction enzymes are used to make recombinant DNA 3. Genes can

More information

DNA & Protein Synthesis UNIT D & E

DNA & Protein Synthesis UNIT D & E DNA & Protein Synthesis UNIT D & E How this Unit is broken down Chapter 10.1 10.3 The structure of the genetic material Chapter 10.4 & 10.5 DNA replication Chapter 10.6 10.15 The flow of genetic information

More information

DNA REPLICATION REVIEW

DNA REPLICATION REVIEW Biology Ms. Ye DNA REPLICATION REVIEW 1. Number the steps of DNA replication the correct order (1, 2, 3): Name Date Block Daughter strands are formed using complementary base pairing DNA unwinds The DNA

More information

DNA/RNA STUDY GUIDE. Match the following scientists with their accomplishments in discovering DNA using the statement in the box below.

DNA/RNA STUDY GUIDE. Match the following scientists with their accomplishments in discovering DNA using the statement in the box below. Name: Period: Date: DNA/RNA STUDY GUIDE Part A: DNA History Match the following scientists with their accomplishments in discovering DNA using the statement in the box below. Used a technique called x-ray

More information

Polymerase Chain Reaction (PCR)

Polymerase Chain Reaction (PCR) Laboratory for Environmental Pathogens Research Department of Environmental Sciences University of Toledo Polymerase Chain Reaction (PCR) Background information The polymerase chain reaction (PCR) is an

More information

TRANSCRIPTION AND PROCESSING OF RNA

TRANSCRIPTION AND PROCESSING OF RNA TRANSCRIPTION AND PROCESSING OF RNA 1. The steps of gene expression. 2. General characterization of transcription: steps, components of transcription apparatus. 3. Transcription of eukaryotic structural

More information

AP Biology Gene Expression/Biotechnology REVIEW

AP Biology Gene Expression/Biotechnology REVIEW AP Biology Gene Expression/Biotechnology REVIEW Multiple Choice Identify the choice that best completes the statement or answers the question. 1. Gene expression can be a. regulated before transcription.

More information

Laboratory #7 PCR PCR

Laboratory #7 PCR PCR 1 Laboratory #7 Polymerase chain reaction () is DNA replication in a test tube. In vitro enzymatic amplification of a specific segment of DNA. Many Applications. direct cloning from DNA or cdna. Mutagenesis

More information

Sequence Databases and database scanning

Sequence Databases and database scanning Sequence Databases and database scanning Marjolein Thunnissen Lund, 2012 Types of databases: Primary sequence databases (proteins and nucleic acids). Composite protein sequence databases. Secondary databases.

More information

DNA DNA Profiling 18. Discuss the stages involved in DNA profiling 19. Define the process of DNA profiling 20. Give two uses of DNA profiling

DNA DNA Profiling 18. Discuss the stages involved in DNA profiling 19. Define the process of DNA profiling 20. Give two uses of DNA profiling Name: 2.5 Genetics Objectives At the end of this sub section students should be able to: 2.5.1 Heredity and Variation 1. Discuss the diversity of organisms 2. Define the term species 3. Distinguish between

More information

Chromosomes. Chromosomes. Genes. Strands of DNA that contain all of the genes an organism needs to survive and reproduce

Chromosomes. Chromosomes. Genes. Strands of DNA that contain all of the genes an organism needs to survive and reproduce Chromosomes Chromosomes Strands of DNA that contain all of the genes an organism needs to survive and reproduce Genes Segments of DNA that specify how to build a protein genes may specify more than one

More information