Porter K W, Tomasz J, Huang F, Sood A, Shaw B R
Department of Chemistry, Duke University, Durham, North Carolina 27708, USA.
Biochemistry. 1995 Sep 19;34(37):11963-9. doi: 10.1021/bi00037a038.
The 5'-triphosphate of the boronated nucleoside analog N7-cyanoborane-2'-deoxyguanosine (7bdGTP) was synthesized, and a series of experiments was initiated to assess the potential of the compound to serve as a substrate for DNA polymerases. We show here that 7bdGTP can be incorporated into DNA by Sequenase. The resulting hemiboronated extension products are resistant to cleavage by treatment with either DMS and heat or a number of restriction enzymes. Further, in the polymerase chain reaction, 7bdGTP can be utilized as a substrate for Taq polymerase. Finally, by kinetic analysis, we have found that 7bdGTP is a more efficient substrate for exonuclease-free Klenow than normal dGTP. Thus, the introduction of a cyanoborane moiety to the N7 position of dGTP results in a nucleotide that is accepted in lieu of normal dGTP by a number of DNA polymerases.
合成了硼化核苷类似物N7-氰基硼烷-2'-脱氧鸟苷(7bdGTP)的5'-三磷酸,并开展了一系列实验以评估该化合物作为DNA聚合酶底物的潜力。我们在此表明,7bdGTP可被测序酶掺入DNA中。所得的半硼化延伸产物在用二甲基亚砜(DMS)和加热处理或多种限制酶处理时对切割具有抗性。此外,在聚合酶链反应中,7bdGTP可被用作Taq聚合酶的底物。最后,通过动力学分析,我们发现7bdGTP是无外切核酸酶的Klenow片段比正常dGTP更有效的底物。因此,在dGTP的N7位引入氰基硼烷部分会产生一种核苷酸,它可被多种DNA聚合酶接受以替代正常的dGTP。