Home / Articles / Pak Agri Outlook / Polymerase Chain Reaction

Polymerase Chain Reaction




  • It is hard to overstate the impact of the polymerase chain reaction. PCR, the quick, easy method for generating unlimited copies of any fragment of DNA, is one of those scientific developments that actually deserve timeworn superlatives like “revolutionary” and “breakthrough.”

    Purpose of PCR

    • Amplify specific nucleic acids in vitro (“Xeroxing” DNA)
    • PCR will allow a short stretch of DNA (usually fewer than 3000 base pairs) to be amplified to about a million fold
    • This amplified sample then allows for size determination and nucleotide sequencing
    • Introduced in 1985 by Kary Mullis
    • Millions of copies of a segment of DNA can be made within a few hours.

    Three Steps

    • Separation: Double Stranded DNA is denatured by heat into single strands.
    • Short Primers for DNA replication are added to the mixture.
    • DNA polymerase catalyzes the production of complementary new strands.
    • Copying The process is repeated for each new strand created
    • All three steps are carried out in the same vial but at different temperatures

    Step 1: Separation

    • Combine Target Sequence, DNA primers template, dNTPs, TAQ Polymerase
    • Target Sequence: Usually fewer than 3000 bp
      • Identified by a specific pair of DNA primers- usually oligonucleotides that are about 20 nucleotides
    • Heat to 95 degrees Celsius to separate strands (for 0.5-2 minutes)
      • Longer times increase denaturation but decrease enzyme and template

    Magnesium as a Cofactor

    • Stabilizes the reaction between:
      • oligonucleotides and template DNA
      • DNA Polymerase and template DNA

    Heat Denatures DNA by uncoiling the Double Helix strands.

    dna

    Step 2: Priming

    • Decrease temperature by 15-25 degrees
    • Primers anneal to the end of the strand
    • 5-2 minutes
    • Shorter time increases specificity but decreases yield
    • Requires knowledge of the base sequences of the 3’ – end

    dna 2

    Selecting a Primer

    • Primer length
    • Melting Temperature (Tm)
    • Specificity
    • Complementary Primer Sequences
    • G/C content and Polypyrimidine (T, C) or polypurine (A, G) stretches
    • 3’-end Sequence
    • Single-stranded DNA

    Step 3: Polymerization

    • Since the Taq polymerase works best at around 75 degrees C (the temperature of the hot springs where the bacterium was discovered), the temperature of the vial is raised to 72-75 Degrees Celsius
    • The DNA polymerase recognizes the primer and makes a complementary copy of the template which is now single stranded.
    • Approximately 150 nucleotides/sec

    dna 3

    Potential Problems with Taq

    • Lack of proof-reading of newly synthesized DNA.
    • Potentially can include diNucleotriphosphates (dNTPs) that are not complementary to the original strand.
    • Errors in coding result
    • Recently discovered thermostable DNA polymerases, Tli and Pfu, are less efficient, yet highly
    • Amplification

    dna 4

    dna 5

    PCR Applications

    • Detection of infectious diseases
    • Detection of variations and mutations in genes
    • Detection of diseases from the past
    • PCR and the law

    Detection of Variations and Mutations in Genes

    • Detects people with inherited disorders
    • Lets us know who carries deleterious variations (mutations)
    • Direct way of distinguishing among the confusion of different mutations in a single gene. Ex: Duchenne muscular dystrophy
    • Track presence or absence of DNA abnormalities characteristic to cancer

    Detection of diseases from the past

    • Presidential candidate Humphreys-had cancer
    • John Dalton-was colored blind and realized that this was the case because he lacked a gene for one of the three photopigments, which caused him to be color blind

    Future of PCR:

    • Copying larger pieces of DNA
    • Miniaturization of hardware (chip-sized devices)
    • Computer automated test and analysis
    • Taking PCR on the road and getting on the spot DNA analysis
    • Diagnose infection or genetic disorder right in the doctors office

    Authors: M.Mohsin Raza1,Samiullah2,M.Hassan3,Maratab4 ali,Hafiz Muhammed bilal1

    The authors of this article are associated with

    1 Institute of soil and environmental sciences university of agriculture Faisalabad Pakistan

    2 Department of Agronomy University of agriculture Faisalabad Pakistan

    3 center for agriculture biochemistry and Biotechnology University of agriculture Faisalabad Pakistan

    4 National institutes of food science and Technology University of agriculture Faisalabad Pakistan

    They can be reached at <mohsinraza_5@yahoo.com, samisheen14@gmail.com>

     

    About Staff

    This post is published by AgriHunt staff member. If you believe it should have your name please contact md@agrihunt.com

    Check Also

    smog lahore

    دھوئیں میں لپٹا ہوا لاہور اور سرسبز شہر کا خواب

    Report Issue: * Suggest Edit Copyright Infringment Claim Article Invalid Contents Broken Links Your Name: …

    Leave a Reply

    Be the First to Comment!

    Notify of
    avatar

    wpDiscuz