Amplification of fluorescent DNA through enzymatic incorporation of a highly emissive deoxyguanosine analogue

Abstract

A highly emissive thio-analogue of deoxyguanosine triphosphate, ^thdGTP, was synthesized and enzymatically incorporated into DNA through primer extension and PCR amplification. The straightforward amplification of ^thdG-labeled DNA by natural polymerases and simple addition of ^thdGTP to the standard PCR mix was demonstrated. The present results will facilitate the broad application of long fluorescent DNA.