Polymerase Chain Reaction (PCR) and Its Applications

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1 Polymerase Chain Reaction (PCR) and Its Applications

2 What is PCR? PCR is an exponentially progressing synthesis of the defined target DNA sequences in vitro. It was invented in 1983 by Dr. Kary Mullis, for which he received the Nobel Prize in Chemistry in 1993.

3 What is PCR? : Why Polymerase? It is called polymerase because the only enzyme used in this reaction is DNA polymerase.

4 What is PCR? : Why Chain? It is called chain because the products of the first reaction become substrates of the following one, and so on.

5 What is PCR? : The Reaction Components 1) Target DNA - contains the sequence to be amplified. 2) Pair of Primers - oligonucleotides that define the sequence to be amplified. 3) dntps - deoxynucleotidetriphosphates: DNA building blocks. 4) Thermostable DNA Polymerase -enzyme that catalyzes the reaction 5) Mg ++ ions - cofactor of the enzyme 6) Buffer solution maintains ph and ionic strength of the reaction solution suitable for the activity of the enzyme

6 PCR Targets The number of bases in the targets can vary. TTAAGGCTCGA.... AATTGGTTAA The.... Represents the middle DNA sequence, and does not have to be known to replicate it.

7 The Reaction PCR tube THERMOCYCLER

8 Denature (heat to 95 o C) Lower temperature to 56 o C Anneal with primers Increase temperature to 72 o C DNA polymerase + dntps

11 DNA copies vs Cycle number DNA copies Cycle number

12 PCR Denaturing Denaturing is the first step in PCR, in which the DNA strands are separated by heating to 95 C.

13 PCR Primers Primers range from 15 to 30 nucleotides, are single-stranded, and are used for the complementary building blocks of the target sequence.

14 PCR Primers A primer for each target sequence on the end of your DNA is needed. This allows both strands to be copied simultaneously in both directions.

15 PCR Primers TTAACGGCCTTAA... TTTAAACCGGTT AATTGCCGGAATT > and < AAATTTGGCCAA TTAACGGCCTTAA... TTTAAACCGGTT

16 PCR Primers The primers are added in excess so they will bind to the target DNA instead of the two strands binding back to each other.

17 PCR Annealing Annealing is the process of allowing two sequences of DNA to form hydrogen bonds. The annealing of the target sequences and primers is done by cooling the DNA to 55 C.

18 PCR Taq DNA Polymerase Taq stands for Thermus aquaticus, which is a microbe found in 176 F hot springs in Yellow Stone National Forest.

19 PCR Taq DNA Polymerase Taq produces an enzyme called DNA polymerase, that amplifies the DNA from the primers by the polymerase chain reaction, in the presence of Mg.

20 Applications of PCR Classification of organisms Genotyping Molecular archaeology Mutagenesis Mutation detection Sequencing Cancer research Detection of pathogens DNA fingerprinting Drug discovery Genetic matching Genetic engineering Pre-natal diagnosis

21 Applications of PCR Basic Research Mutation screening Drug discovery Classification of organisms Genotyping Molecular Archaeology Molecular Epidemiology Molecular Ecology Bioinformatics Genomic cloning Site-directed mutagenesis Gene expression studies Applied Research Genetic matching Detection of pathogens Pre-natal diagnosis DNA fingerprinting Gene therapy

22 Applications of PCR Molecular Identification Sequencing Genetic Engineering Molecular Archaeology Molecular Epidemiology Molecular Ecology DNA fingerprinting Classification of organisms Genotyping Pre-natal diagnosis Mutation screening Drug discovery Genetic matching Detection of pathogens Bioinformatics Genomic cloning Human Genome Project Site-directed mutagenesis Gene expression studies

23 MOLECULAR IDENTIFICATION:

25 Molecular Identification: Detection of Unknown Mutations

26 SSCP gels: shifts representing a mutation in the amplified DNA fragment

27 Molecular Identification: Classification of Organisms 1) Relating to each other 2) Similarities 3) Differences * Fossils * Trace amounts * Small organisms Insufficient data! DNA!

29 Rademaker et al. 2001

30 Molecular Identification: Detection Of Pathogens

31 Molecular Identification: Detection Of Pathogens Sensitivity of detection of PCR-amplified M. tuberculosis DNA. (Kaul et al.1994)

32 Sensitivity of detection of PCR-amplified M. tuberculosis DNA. (Kaul et al.1994)

33 Molecular Identification: Genotyping by STR markers

34 Molecular Identification: Prenatal Diagnosis Chorionic Villus Amniotic Fluid 644 bp 440 bp 204 bp Molecular analysis of a family with an autosomal recessive disease.

35 SEQUENCING Nucleotides (dntp) are modified (dideoxynucleotides = ddntp) NO polymerisation after a dideoxynucleotide! Fragments of DNA differing only by one nucleotide are generated Nucleotides are either or

36 Sequencing:

37 Summary blood, chorionic villus, amniotic fluid, semen, hair root, saliva 68,719,476,736 copies Gel Analysis, Restriction Digestion, Sequencing

38 Conclusion The speed and ease of use, sensitivity, specificity and robustness of PCR has revolutionised molecular biology and made PCR the most widely used and powerful technique with great spectrum of research and diagnostic applications.

Polymerase Chain Reaction PCR

Polymerase Chain Reaction PCR What is PCR? An in vitro process that detects, identifies, and copies (amplifies) a specific piece of DNA in a biological sample. Discovered by Dr. Kary Mullis in 1983. A