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UvrD helicase: An old dog with a new trick How one step backward leads to many steps forward

机译:UvrD解旋酶:老狗新技巧

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摘要

Transcription-coupled repair (TCR) is a phenomenon that exists in a wide variety of organisms from bacteria to humans. This mechanism allows cells to repair the actively transcribed DNA strand much faster than the non-transcribed one. At the sites of bulky DNA damage RNA polymerase stalls, initiating recruitment of the repair machinery. It is a commonly accepted paradigm that bacterial cells utilize a sole coupling factor, called Mfd to initiate TCR. According to that model, Mfd removes transcription complexes stalled at the lesion site and simultaneously recruits repair machinery. However, this model was recently put in doubt by various discrepancies between the proposed universal role of Mfd in the TCR and its biochemical and phenotypical properties. Here, I present a second pathway of bacterial TCR recently discovered in my laboratory, which does not involve Mfd but implicates a common repair factor, UvrD, in a central position in the process.
机译:转录偶联修复(TCR)是一种广泛存在的现象,从细菌到人类。这种机制使细胞修复主动转录的DNA链比非转录的DNA链修复快得多。在庞大的DNA损伤位点,RNA聚合酶失速,启动了修复机制的募集。细菌细胞利用称为Mfd的唯一偶联因子来引发TCR是一种普遍接受的范例。根据该模型,Mfd去除停滞在病变部位的转录复合物,同时募集修复工具。但是,该模型最近因Mfd在TCR中的普遍作用与其生化和表型特性之间的各种差异而受到质疑。在这里,我介绍了在我的实验室中最近发现的细菌TCR的第二种途径,该途径不涉及Mfd,但在该过程的中心位置牵涉到一个常见的修复因子UvrD。

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