Washington M Todd, Johnson Robert E, Prakash Louise, Prakash Satya
Sealy Center for Molecular Science, University of Texas Medical Branch at Galveston, 6.104 Blocker Medical Research Building, 11th and Mechanic Streets, Galveston, TX 77555-1061, USA.
Mol Cell Biol. 2004 Jan;24(2):936-43. doi: 10.1128/MCB.24.2.936-943.2004.
Human DNA polymerase iota (Poliota) is a member of the Y family of DNA polymerases involved in translesion DNA synthesis. Poliota is highly unusual in that it possesses a high fidelity on template A, but has an unprecedented low fidelity on template T, preferring to misincorporate a G instead of an A. To understand the mechanisms of nucleotide incorporation opposite different template bases by Poliota, we have carried out pre-steady-state kinetic analyses of nucleotide incorporation opposite templates A and T. These analyses have revealed that opposite template A, the correct nucleotide is preferred because it is bound tighter and is incorporated faster than the incorrect nucleotides. Opposite template T, however, the correct and incorrect nucleotides are incorporated at very similar rates, and interestingly, the greater efficiency of G misincorporation relative to A incorporation opposite T arises predominantly from the tighter binding of G. Based on these results, we propose that the incipient base pair is accommodated differently in the active site of Poliota dependent upon the template base and that when T is the templating base, Poliota accommodates the wobble base pair better than the Watson-Crick base pair.
人类DNA聚合酶ι(Poliota)是参与跨损伤DNA合成的Y家族DNA聚合酶成员。Poliota非常特别,因为它在模板A上具有高保真度,但在模板T上具有前所未有的低保真度,更倾向于错误掺入G而非A。为了理解Poliota在不同模板碱基对面掺入核苷酸的机制,我们对模板A和T对面的核苷酸掺入进行了预稳态动力学分析。这些分析表明,在模板A对面,正确的核苷酸更受青睐,因为它结合更紧密且掺入速度比错误的核苷酸更快。然而,在模板T对面,正确和错误的核苷酸掺入速率非常相似,有趣的是,相对于在T对面掺入A,G错误掺入的效率更高主要源于G的结合更紧密。基于这些结果,我们提出,初始碱基对在Poliota的活性位点中的容纳方式因模板碱基而异,并且当T作为模板碱基时,Poliota对摆动碱基对的容纳优于沃森-克里克碱基对。