Suppr超能文献

大肠杆菌中的Y家族DNA聚合酶。

Y-family DNA polymerases in Escherichia coli.

作者信息

Jarosz Daniel F, Beuning Penny J, Cohen Susan E, Walker Graham C

机构信息

Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

出版信息

Trends Microbiol. 2007 Feb;15(2):70-7. doi: 10.1016/j.tim.2006.12.004. Epub 2007 Jan 4.

Abstract

The observation that mutations in the Escherichia coli genes umuC+ and umuD+ abolish mutagenesis induced by UV light strongly supported the counterintuitive notion that such mutagenesis is an active rather than passive process. Genetic and biochemical studies have revealed that umuC+ and its homolog dinB+ encode novel DNA polymerases with the ability to catalyze synthesis past DNA lesions that otherwise stall replication--a process termed translesion synthesis (TLS). Similar polymerases have been identified in nearly all organisms, constituting a new enzyme superfamily. Although typically viewed as unfaithful copiers of DNA, recent studies suggest that certain TLS polymerases can perform proficient and moderately accurate bypass of particular types of DNA damage. Moreover, various cellular factors can modulate their activity and mutagenic potential.

摘要

大肠杆菌基因umuC⁺和umuD⁺中的突变会消除紫外线诱导的诱变作用,这一观察结果有力地支持了一个与直觉相悖的观点,即这种诱变是一个主动而非被动的过程。遗传和生化研究表明,umuC⁺及其同源基因dinB⁺编码新型DNA聚合酶,这些聚合酶能够催化越过那些会使复制停滞的DNA损伤进行合成——这一过程称为跨损伤合成(TLS)。几乎在所有生物体中都鉴定出了类似的聚合酶,它们构成了一个新的酶超家族。尽管通常被视为DNA的不忠实复制者,但最近的研究表明,某些TLS聚合酶能够高效且适度准确地绕过特定类型的DNA损伤。此外,各种细胞因子可以调节它们的活性和诱变潜力。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验