What does 'prevention of nontemplate-directed nucleotide addition' mean? - (Nov/22/2012 )
A friend of mine asked me a question I couldn't answer. He gave me a paper (as attached) and asked me why there is a
F: 6-FAM TCAACTGTTGGAAGGGCAAT
In the legend of Table 2 it reads " The
Apparently after PCR they analyse the product with an ABI machine.
PCR of repeats is used to measure their length, which is highly polymorphic. But since Taq ads additional A at the end in presumably (from the paper) unpredictible manner, and together with the fact that polymerase may slip on the repeats, it then creates multiple products from one reaction, differing around that one nucleotide.
Products are marked by fluorescent fwd primer and analysed in capillary electrophoresis (similar as sequencing). But the you got multiple signals for one length and if you are looking into dinucleotide repeats for example, it's really difficult to measure the right length then.
This is for the explanation why this is needed.
This seems to be the original paper about the added A.
Maybe more will be found in key papers about STR polymorfisms, like this one maybe, but I don't have the access. Validation of short tandem repeats (STRs) for forensic usage: performance testing of fluorescent multiplex STR systems and analysis of authentic and simulated forensic samples.
But from search seems, that adding tails (not just this particular sequence) is a common thing in STR amplification.
Keep me posted if you find out
Thanks Trof, I sent your reply to my friend. I don't have time to read the papers today, but I also want to find out if the sequence of the tail is important or not....or it can be anything?
I think the paper states, the tail makes the A adding more reproducible instead of just simply abrogating it, so the mechanism may be really complex.