Review? - What are the four macromolecules?

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Transcription:

Review? - What are the four macromolecules? Lipids Carbohydrates Protein Nucleic Acids What is the monomer of nucleic acids and what do nucleic acids make up? Nucleotides; DNA and RNA

12-1 DNA

DNA Stands for DNA: Deoxyribonucleic acid Very large biomolecule made up of monomers called nucleotides Called the blueprints of life because it contains genetic information for the construction of proteins to make up who we are.

Quick Refresher - Where is DNA located? Floats freely in the cytoplasm of DNA is protected in the nucleus of.

Chromosomes and DNA A gene is a segment of DNA. Genes are organized and packaged in units called chromosomes. Each gene codes for a certain protein. 5

DNA is made of nucleotides Nucleotide is a monomer of nucleic acids made up of 3 parts Deoxyribose sugar (5-carbon sugar) Phosphate group Nitrogen base (4 kinds) Adenine (A) Guanine (G) Cytosine (C) Thymine (T)

Base Pair Rule (Chargaff s Rule): Adenine pairs with Thymine (straight letters) Guanine pairs with Cytosine (curved letters)

Base Pair Rule Practice What is the complimentary base sequence for A T G C T A C G C

DNA Structure Made of 2 strands that wrap around each other to form a double helix (looks like a spiral staircase) The sides (a.k.a. the backbone) : Alternating Sugar, phosphate, sugar, phosphate The middle: Nitrogen bases paired together. (A-T, and C-G)

Q: DNA is a long molecule made of monomers called a. nucleotides. b. purines. c. pyrimidines. d. sugars. Copyright Pearson Prentice Hall

Q: In DNA, the following base pairs occur: a. A with C, and G with T. b. A with T, and C with G. c. A with G, and C with T. d. A with T, and C with T. Copyright Pearson Prentice Hall

12 2 Chromosomes and DNA Replication 12-2 Chromosomes and DNA Replication Copyright Pearson Prentice Hall

Replication of DNA DNA molecules can build an exact copy of itself. This is called Replication. Replication is important for reproduction and must occur every time a cell divides.

Steps to DNA Replication 1. In the nucleus, weak hydrogen bonds break between the nitrogen bases of DNA (A, T, G, C). 2. This causes the DNA to unzip like a zipper. 3. Enzymes in the nucleus, called DNA Polymerase, directs free floating nucleotides in the nucleus to attach to each strand following the rules of base pairing. 4. Each strand serves as a template for the new strand. 5. This results in two identical strands of DNA. 6. This is called Semi- Conservative Replication, producing two copies of DNA that each contain one of the original strands Semi - Conservative Replication Video

DNA Replication New Strand Original strand Nitrogen Bases Growth Growth Replication Fork Replication Fork DNA polymerase joins individual nucleotides to produce a DNA molecule and then proofreads each new DNA strand to check Copyright Pearson Prentice Hall for errors and fix them. DNA Polymerase

Q: The first step in DNA replication is a. producing two new strands. b. separating the strands by breaking hydrogen bonds. c. producing DNA polymerase. d. correctly pairing bases. Copyright Pearson Prentice Hall

Q: A DNA molecule separates, and the sequence GCGAATTCG occurs in one strand. What is the base sequence on the other strand? a. GCGAATTCG b. CGCTTAAGC c. TATCCGGAT d. GATGGCCAG Copyright Pearson Prentice Hall

Q: In addition to carrying out the replication of DNA, the enzyme DNA polymerase also functions to a. unzip the DNA molecule. b. regulate the time copying occurs in the cell cycle. c. proofread the new copies to minimize the number of mistakes. d. wrap the new strands onto histone proteins. Copyright Pearson Prentice Hall

12-3 RNA and Protein Synthesis

What is protein Synthesis?

What are PROTEINS? A category of molecules, each with a unique shape, found EVERYWHERE in your body, required for the structure and function of our body: Proteins comprise: Bone and Teeth Muscle Cartilage Skin Nails Hair Hemoglobin Enzymes Antibodies

Q: Do you remember the four macromolecules (we just reviewed this)? Lipids Proteins Carbohydrates Nucleic Acid Q: What monomer makes up proteins? Amino Acids

Proteins (polymers) are made up of long chains of amino acids (monomers) attached together. There are 20 different kinds of amino acids found in living things There are thousands, maybe millions, of different kinds of proteins in living things.

Imagine that the twenty kinds of amino acids are like twenty different kinds of beads in a bead kit and we have an unlimited supply of them.

You could make an infinite number of different necklaces from just those 20 different kinds of beads. Different colors, sequences, shapes, and lengths EACH NECKLACE HAS A DIFFERENT FUNCTION

Likewise, there are endless kinds of proteins that can be made from only 20 different amino acids, and each protein is a different function in living things! Chain of amino acids protein

Overview of Protein Synthesis - the process to make a protein? DNA code RNA code Protein Transcription mrna molecule is transcribed from DNA (takes place in the nucleus) Translation protein built from mrna code (takes place in the cytoplasm)

Q: What is RNA RNA stands for ribonucleic acid RNA is like DNA (it s comprised of nucleotides), with a few differences: Sugar is different (ribose instead of deoxyribose) Nitrogen-containing bases include: Adenine Cytosine Guanine Uracil (not Thymine!!) RNA is a single stranded (not double.the bases are unpaired)

3 Types of RNA Types of RNA There are three main types of RNA: messenger RNA ribosomal RNA transfer RNA Copyright Pearson Prentice Hall

Messenger RNA Messenger RNA (mrna) the mirror image of a DNA code (except Uracil replaces Thymine); serves as the template from which proteins (specific amino acid sequences) are built, Carries code from the nucleus to the ribosomes.

Ribosomal RNA Ribosomal RNA (rrna) Ribosomes are made up of proteins and ribosomal RNA (rrna). reads the mrna code during protein synthesis

Transfer RNA Transfer RNA (trna) found in the cytoplasm, delivers one amino acid to the ribosome during protein synthesis Growing amino acid chain to make a protein Place of rrna

TRANSCRIPTION The process by which a mrna molecule is constructed from a DNA code; occurs in the nucleus of a cell 1. With the help of enzymes (RNA polymerase), DNA and separates the DNA strands. 2. RNA polymerase then uses one strand of DNA as a template from which nucleotides are assembled into a single strand of RNA 3. The mrna strand detaches from the DNA 4. The DNA re-zips Remember: RNA does not have the nucleotide Thymine, but has Uracil instead, so the Adenine on DNA with base pair with Uracil (A=U) animation

Transcription RNA RNA polymerase DNA Copyright Pearson Prentice Hall

Lets Practice Given the DNA sequence below, what would be the mrna code? A T T C G G G A T A A C C T

The Genetic Code A codon consists of three consecutive nucleotides on mrna that specify a particular amino acid that will build the protein. Copyright Pearson Prentice Hall

Some amino acids can be specified by more than one codon. The Genetic Code Copyright Pearson Prentice Hall

animation TRANSLATION Translation is the decoding of an mrna message into a polypeptide chain to make a protein. Translation takes place on ribosomes. During translation, the cell uses information from messenger RNA to produce proteins.

Before translation begins.. Messenger RNA is transcribed in the nucleus, and then enters the cytoplasm where it attaches to a ribosome. Nucleus mrna Copyright Pearson Prentice Hall

Translation Translation begins when an mrna molecule attaches to a ribosome and the start codon AUG is read, signifying the start of the amino acid chain. As each codon of the mrna molecule moves through the ribosome, the proper amino acid is brought into the ribosome by trna. In the ribosome, the amino acid is transferred to the growing amino acid chain. Copyright Pearson Prentice Hall

Translation - trna In addition to an amino acid, each trna molecule has three unpaired bases. These bases, called the anticodon, are complementary to one mrna codon. Copyright Pearson Prentice Hall

The ribosome binds new trna molecules and amino acids as it moves along the mrna. trna molecules are reused to get more amino acids. Methionine Phenylalanine trna Lysine Ribosome mrna Start codon Copyright Pearson Prentice Hall

The process continues until the ribosome reaches a stop codon, signifying the end of the polypeptide. Polypeptide trna Ribosome mrna Copyright Pearson Prentice Hall

Q: A base that is present in RNA but NOT in DNA is a. thymine. b. uracil. c. cytosine. d. adenine. Copyright Pearson Prentice Hall

Q: The nucleic acid responsible for bringing individual amino acids to the ribosome is a. transfer RNA. b. DNA. c. messenger RNA. d. ribosomal RNA. Copyright Pearson Prentice Hall

Q: A codon typically carries sufficient information to specify a(an) a. single base pair in RNA. b. single amino acid. c. entire protein. d. single base pair in DNA. Copyright Pearson Prentice Hall

Transcription and Translation label the following diagram using the following terms polypeptide (protein) DNA trna mrna Amino acid ribosome codon anticodon

OPTIONAL - PRACTICE WITH THE CODE -transcription and translationlearn.genetics.utah.edu/units/basics/transcribe

. 12.4 Mutations Copyright Pearson Prentice Hall

What Are Mutations? Changes in the nucleotide sequence of DNA May occur in somatic cells(body cells), these are passed to offspring May occur in gametes(sex cells) and can be passed to offspring

Kinds of Mutations Mutations that produce changes in a single gene are known as gene mutations. Mutations that produce changes in whole chromosomes are known as chromosomal mutations.

Gene Mutations Gene mutations involving a change in one or a few nucleotides are known as point mutations because they occur at a single point in the DNA sequence. Point mutations include substitutions, insertions, and deletions. Copyright Pearson Prentice Hall

Kinds of Gene Mutations Substitutions usually affect no more than a single amino acid. A base is substituted for another base. Copyright Pearson Prentice Hall

Sickle Cell disease is the result of one nucleotide substitution

Kinds of Gene Mutations The effects of insertions or deletions are more dramatic. The addition or deletion of a nucleotide causes a shift in the grouping of codons, therefore proteins are built incorrectly. Changes like these are called frameshift mutations. Predict: What will happen to the amino acid sequence? Copyright Pearson Prentice Hall

Kinds of Gene Mutations In an insertion, an extra base is inserted into a base sequence. Copyright Pearson Prentice Hall

In a deletion, the loss of a single base is deleted and the reading frame is shifted. Amino Acid Sequence Changed

Chromosomal Mutations Kinds of Chromosomal Mutations Chromosomal mutations involve changes in the number or structure of chromosomes, break or are lost during mitosis or meiosis. Chromosomal mutations include deletions, duplications, inversions, and translocations. Copyright Pearson Prentice Hall

Kinds of Chromosomal Mutations Deletions involve the loss of all or part of a chromosome. Copyright Pearson Prentice Hall

Kinds of Chromosomal Mutations Duplications produce extra copies of parts of a chromosome (sequence repeated). Copyright Pearson Prentice Hall

Kinds of Mutations Inversions reverse the direction of parts of chromosomes. Copyright Pearson Prentice Hall

Kinds of Chromosomal Mutations Translocations occurs when part of one chromosome breaks off and attaches to another. Copyright Pearson Prentice Hall

Are Mutations Helpful or Harmful? Mutations happen regularly Almost all mutations are neutral Chemicals & UV radiation cause mutations Many mutations are repaired by enzymes Do you remember the name of that enzyme? DNA polymerase

Are Mutations Helpful or Harmful? Some type of skin cancers and leukemia result from somatic (body cell) mutations Some mutations may improve an organism s survival (beneficial)

Q: The type of point mutation that usually affects only a single amino acid is called a. a deletion. b. a frameshift mutation. c. an insertion. d. a substitution. Copyright Pearson Prentice Hall

Q: A mutation that affects every amino acid following an insertion or deletion is called a(an) a. frameshift mutation. b. point mutation. c. chromosomal mutation. d. inversion. Copyright Pearson Prentice Hall

Q: When two different chromosomes exchange some of their material, the mutation is called a(an) a. inversion. b. deletion. c. substitution. d. translocation. Copyright Pearson Prentice Hall