Silver: PCR

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DESIGN & PREPARATION OF OLIGONUCLEOTIDE INSERTS FOR INSERTS ~ 85 BP AND LARGER: PRIMER AMPLIFICATION OF YEAST DNA

A. Primer design for PCR

  • For typical BioBricks construction, you want a PCR product which has an XbaI site upstream of your part, and SpeI, NotI, and PstI sites downstream of your part.
    Then, the forward primer should be of the form:
    5' CCTTTCTAGA (15-20 bp complement to coding strand) 3'
    and the reverse primer should be of the form:
    5' AAGGCTGCAGCGGCCGCTACTAGT (15-20 bp reverse complement) 3'
  • Design considerations. Make sure that:
    • The Tm of each primer is between 55-65 °C
    • The Tm of both primers are very similar, i.e., within ~2 °C
    • Either primer will not form a stable internal hairpin structure, i.e., ΔG <-3 kcal/mol
    • The forward and reverse primers do not combine to form a stable hairpin structure or dimer
    • The genomic DNA to be amplified does not contain any EcoRI, PstI, SpeI, XbaI, or AarI sites
    • The insert for the forward primer does not begin with TC (or else a DAM I site (GATC) is formed, and XbaI cannot cut)
    • If possible the 3' end of each primer should end with a GC
  • An easy way to design primers is to use Vector NTI.
    1. Find the genomic DNA sequence that you want to amplify as your part at yeastgenome.org and save it into Vector NTI.
    2. Highlight the sequence that you want as your part, and select Analyses -> Primer Design -> Amplify Selection.
    3. Under the Primer tab, set "Before" and "After" to 0 bp. Adjust the Tm, primer length, GC content, et c. as noted above. Also click More>> and insert the flanking sense and anti-sense sequences (given at top) in the boxes "Attach to 5' terminus of Sense primer" and "Attach to 5' terminus of Anti-sense primer". Lastly, click "Apply" then "OK."
    4. Three possible sets of designed primers will appear in a folder on the left side of the screen, ranked by their score. Usually, the best possible score is 171. The lowest score that I (Caroline) have successfully used is ~120.
    5. Double-check your primers by highlighting a given sequence, then right-clicking and selecting "Analyze".
      • For more information, check out Vector NTI's user manual, Chapters 8 and 20.
  • Order 25 nmol DNA oligo with standard desalting from IDT.
  • Note: if it is not possible to make a good set of primers with the flanking regions described above, see if using a different set of flanking regions improves the primers. For example, you can also use a PCR product that has the EcoRI, NotI, and XbaI sites upstream of your part, while the SpeI site is downstream of your part. In this case, the forward primer would be of the form: 5' CCTTGAATTCGCGGCCGCATCTAGA (15-20 bp complement to coding strand)3' and the reverse primer should be of the form:
    5' AAGGACTAGT (15-20 bp complement to coding strand) 3'.

B. PCR from yeast chromosomal or plasmid template

  1. Resuspend each primer in Tris buffer pH 8.0 or distilled water to 100 µM.
  2. Mix:
    • 5 µL 10x ThermoPol buffer
    • 0.4 µL 25 mM dNTPs
    • 0.5 µL 100 µM forward primer
    • 0.5 µL 100 µM reverse primer
    • ≤1 µL plasmid DNA or 2 µL genomic DNA
    • 1 µL Vent DNA polymerase
    • distilled water to 50 µL total volume
  3. PCR program:
    • Start: 95 °C for 2 min. (melt)
    • Cycle 95 °C for 0.5 min (melt)
    • Tm minus 5 °C for 0.5 min. (anneal)
    • 74 °C for (# bp/1000) min. (extension) - no less than 0.5 min.
    • No. of Cycles: 30
    • End: keep at 4 °C forever

C. Gel analysis and purification of PCR products

  • Run 2 µL of PCR reaction on an appropriate percentage agarose gel.
  • If only your desired band is present, purify using Qiagen's PCR purification kit and elute with 30 µL.
  • Else, gel extract.
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