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论DNA合成的保真度。焦磷酸诱导的错配掺入可检测两种校对机制。

On the fidelity of DNA synthesis. Pyrophosphate-induced misincorporation allows detection of two proofreading mechanisms.

作者信息

Kunkel T A, Beckman R A, Loeb L A

出版信息

J Biol Chem. 1986 Oct 15;261(29):13610-6.

PMID:3020037
Abstract

The effect of pyrophosphate on the fidelity of in vitro DNA synthesis has been examined. Pyrophosphate enhances misincorporation by Escherichia coli DNA polymerase I in copying phi X174 DNA. The increased misincorporation is directly proportional to the extent of inhibition of the rate of polymerization. In contrast, pyrophosphate is not detectably mutagenic with avian myeloblastosis virus DNA polymerase or DNA polymerases alpha and beta from animal cells, which lack associated proofreading activities. This suggests that increased misincorporation by pyrophosphate is not due to an increase in misinsertions by DNA polymerase, but rather due to inhibition of proofreading by pyrophosphate. However, the pyrophosphate-induced infidelity has a different specificity from, and is not competitive with, two experimental markers of 3'----5' exonuclease proofreading; i.e. the effects of the next nucleotide or the addition of deoxynucleoside monophosphates. These distinctive features suggest a second mode of proofreading susceptible to inhibition by pyrophosphate. This concept is discussed in relation to models for proofreading described in the literature.

摘要

焦磷酸对体外DNA合成保真度的影响已得到研究。焦磷酸在大肠杆菌DNA聚合酶I复制φX174 DNA时会增强错配掺入。错配掺入的增加与聚合速率的抑制程度成正比。相比之下,焦磷酸对禽成髓细胞瘤病毒DNA聚合酶或动物细胞中的DNA聚合酶α和β没有可检测到的诱变作用,这些酶缺乏相关的校对活性。这表明焦磷酸导致的错配掺入增加并非由于DNA聚合酶错插入的增加,而是由于焦磷酸对校对的抑制。然而,焦磷酸诱导的不忠实性与3'→5'核酸外切酶校对的两个实验标记具有不同的特异性,且与之无竞争性;即下一个核苷酸的影响或脱氧单磷酸核苷的添加。这些独特特征提示了一种易受焦磷酸抑制的校对新模式。结合文献中描述的校对模型对这一概念进行了讨论。

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