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人类DNA聚合酶κ利用模板-引物错配作为一种新的方式来延伸错配末端并产生单碱基缺失。

Human DNA polymerase kappa uses template-primer misalignment as a novel means for extending mispaired termini and for generating single-base deletions.

作者信息

Wolfle William T, Washington M Todd, Prakash Louise, Prakash Satya

机构信息

Sealy Center for Molecular Science, University of Texas Medical Branch at Galveston, Galveston, TX 77555-1061, USA.

出版信息

Genes Dev. 2003 Sep 1;17(17):2191-9. doi: 10.1101/gad.1108603.

Abstract

Human DNA polymerase kappa (hPolkappa) is a proficient extender of mispaired primer termini on undamaged DNA, wherein it extends directly by incorporating the next correct nucleotide, generating single-base substitutions in the process. Biochemical and genetic studies, however, have indicated that, in addition to single-base substitutions, Polkappa generates single-base deletions. Here we show that hPolkappa is very adept at using template-primer misalignment as a novel means for extending mispaired termini and for generating single-base deletions. The proficient ability of hPolkappa to extend mispaired primer termini either directly or by misalignment could be important for the continued and efficient progression of the replication fork when mismatches introduced by the replicative polymerase are not proofread. In extending from nucleotides opposite DNA lesions, hPolkappa uses the direct and misalignment modes of mispair extension to different extents, depending on whether the template base is present or not at the primer terminus; thus, although hPolkappa can extend directly from nucleotides opposite damaged bases, it can use only the misalignment mechanism to extend from nucleotides opposite an abasic site. A particularly unconstrained active site at the template-primer junction could afford hPolkappa the ability to tolerate the geometric distortions of mismatched base pairs or those resulting from template-primer misalignment, thereby enabling it to use both of these modes of mispair extension.

摘要

人类DNA聚合酶κ(hPolκ)是未受损DNA上错配引物末端的高效延伸酶,它通过掺入下一个正确的核苷酸直接延伸,在此过程中产生单碱基替换。然而,生化和遗传学研究表明,除了单碱基替换外,Polκ还会产生单碱基缺失。我们在此表明,hPolκ非常擅长利用模板-引物错配作为一种新的方式来延伸错配末端并产生单碱基缺失。当复制性聚合酶引入的错配未被校正时,hPolκ直接或通过错配延伸错配引物末端的高效能力对于复制叉的持续和高效推进可能很重要。在从与DNA损伤相对的核苷酸处延伸时,hPolκ根据引物末端是否存在模板碱基,以不同程度使用错配延伸的直接和错配模式;因此,尽管hPolκ可以从与受损碱基相对的核苷酸处直接延伸,但它只能使用错配机制从与无碱基位点相对的核苷酸处延伸。模板-引物连接处一个特别不受限制的活性位点可能使hPolκ能够耐受错配碱基对或模板-引物错配导致的几何畸变,从而使其能够使用这两种错配延伸模式。

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