Mfd - at the crossroads of bacterial DNA repair, transcriptional regulation and molecular evolvability.

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Transcription-Austin Pub Date : 2021-08-01 Epub Date: 2021-10-21 DOI:10.1080/21541264.2021.1982628
Alexandra M Deaconescu
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Abstract

For survival, bacteria need to continuously evolve and adapt to complex environments, including those that may impact the integrity of the DNA, the repository of genetic information to be passed on to future generations. The multiple factors of DNA repair share the substrate on which they operate with other key cellular machineries, principally those of replication and transcription, implying a high degree of coordination of DNA-based activities. In this review, I focus on progress made in the understanding of the protein factors operating at the crossroads of these three fundamental processes, with emphasis on the mutation frequency decline protein (Mfd, aka TRCF). Although Mfd research has a rich history that goes back in time for more than half a century, recent reports hint that much remains to be uncovered. I argue that besides being a transcription-repair coupling factor (TRCF), Mfd is also a global regulator of transcription and a pro-mutagenic factor, and that the way it interfaces with transcription, replication and nucleotide excision repair makes it an attractive candidate for the development of strategies to curb molecular evolution, hence, antibiotic resistance.

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Mfd--处于细菌 DNA 修复、转录调控和分子可进化性的十字路口。
为了生存,细菌需要不断进化并适应复杂的环境,包括可能影响 DNA 完整性的环境,而 DNA 是遗传信息的宝库,将遗传给后代。DNA 修复的多种因素与其他关键的细胞机制(主要是复制和转录机制)共享其运作的基质,这意味着基于 DNA 的活动需要高度协调。在这篇综述中,我将重点介绍在这三个基本过程的交叉点上运行的蛋白质因子的研究进展,重点是突变频率下降蛋白(Mfd,又名 TRCF)。虽然 Mfd 的研究历史可以追溯到半个多世纪以前,但最近的报告暗示,还有很多东西有待发掘。我认为,Mfd除了是转录-修复偶联因子(TRCF)外,还是转录的全球调控因子和促突变因子,它与转录、复制和核苷酸切除修复的相互作用方式使其成为开发遏制分子进化策略(从而遏制抗生素耐药性)的一个有吸引力的候选因子。
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来源期刊
Transcription-Austin
Transcription-Austin BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
6.50
自引率
5.60%
发文量
9
期刊最新文献
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