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真细菌中转位合成 DNA 聚合酶的生物学作用

Biological roles of translesion synthesis DNA polymerases in eubacteria.

机构信息

Uppsala University, Department of Medical Biochemistry and Microbiology, SE-75123 Uppsala, Sweden.

出版信息

Mol Microbiol. 2010 Aug;77(3):540-8. doi: 10.1111/j.1365-2958.2010.07260.x. Epub 2010 Jun 28.

Abstract

Biological systems are strongly selected to maintain the integrity of their genomes by prevention and repair of external and internal DNA damages. However, some types of DNA lesions persist and might block the replication apparatus. The universal existence of specialized translesion synthesis DNA polymerases (TLS polymerases) that can bypass such lesions in DNA implies that replication blockage is a general biological problem. We suggest that the primary function for which translesion synthesis polymerases are selected is to rescue cells from replication arrest at lesions in DNA, a situation that, if not amended, is likely to cause an immediate and severe reduction in cell fitness and survival. We will argue that the mutagenesis observed during translesion synthesis is an unavoidable secondary consequence of this primary function and not, as has been suggested, an evolved mechanism to increase mutation rates in response to various stresses. Finally, we will discuss recent data on additional roles for translesion synthesis polymerases in the formation of spontaneous deletions and in transcription-coupled TLS, where the coupling of transcription to TLS is proposed to allow the rescue of the transcription machinery arrested at DNA lesions.

摘要

生物系统通过预防和修复内外源 DNA 损伤,强烈选择来维持其基因组的完整性。然而,某些类型的 DNA 损伤仍然存在,并可能阻断复制装置。具有跨损伤合成(TLS)功能的特殊 DNA 聚合酶(TLS 聚合酶)的普遍存在表明,复制受阻是一个普遍的生物学问题。我们提出,跨损伤合成聚合酶被选择的主要功能是挽救细胞免于在 DNA 损伤处发生复制停滞,否则这种情况很可能导致细胞适应性和存活能力的迅速而严重的降低。我们将论证,在跨损伤合成过程中观察到的突变是这种主要功能不可避免的次要后果,而不是如前所述的,是一种进化机制,以响应各种应激增加突变率。最后,我们将讨论关于跨损伤合成聚合酶在自发缺失形成和转录偶联 TLS 中的其他作用的最新数据,其中提出将转录与 TLS 偶联以允许挽救在 DNA 损伤处停滞的转录机制。

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