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Cooperation and competition in mismatch repair: very short-patch repair and methyl-directed mismatch repair in Escherichia coli [Review]

机译:错配修复方面的合作与竞争:大肠杆菌中的非常短片修复和甲基定向错配修复[综述]

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In Escherichia coli and related enteric bacteria, repair of base-base mismatches is performed by two overlapping biochemical processes, methyl-directed mismatch repair (MMR) and very short-patch (VSP) repair. While MMR repairs replication errors, VSP repair corrects to C.G mispairs created by 5-methylcytosine deamination to T. The efficiency of the two pathways changes during the bacterial life cycle; MMR is more efficient during exponential growth and VSP repair is more efficient during the stationary phase. VSP repair and MMR share two proteins, MutS and MutL, and although the two repair pathways are not equally dependent on these proteins, their dual use creates a competition within the cells between the repair processes. The structural and biochemical data on the endonuclease that initiates VSP repair, Vsr, suggest that this protein plays a role similar to MutH (also an endonuclease) in MMR. Biochemical and genetic studies of the two repair pathways have helped eliminate certain models for MMR and put restrictions on models that can be developed regarding either repair process. We review here recent information about the biochemistry of both repair processes and describe the balancing act performed by cells to optimize the competing processes during different phases of the bacterial life cycle. [References: 50]
机译:在大肠杆菌和相关的肠道细菌中,碱基-碱基错配的修复是通过两个重叠的生化过程进行的,分别是甲基化错配修复(MMR)和非常短片(VSP)修复。 MMR修复复制错误,而VSP修复可纠正由5-甲基胞嘧啶脱氨至T所产生的C.G错配。在细菌的生命周期中,这两种途径的效率都会发生变化。 MMR在指数增长期间效率更高,而VSP修复在固定阶段效率更高。 VSP修复和MMR共享两种蛋白MutS和MutL,尽管这两种修复途径并不均等地依赖于这些蛋白,但它们的双重用途在修复过程之间在细胞内产生了竞争。启动VSP修复的核酸内切酶Vsr的结构和生化数据表明,该蛋白在MMR中起着与MutH(也是核酸内切酶)相似的作用。两种修复途径的生化和遗传研究已帮助消除了MMR的某些模型,并限制了可以针对任一修复过程开发的模型。我们在这里回顾有关这两个修复过程的生物化学的最新信息,并描述细胞在细菌生命周期的不同阶段优化细胞竞争过程所执行的平衡作用。 [参考:50]

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