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RNA 聚合酶的考古学:转录周期中的因子交换。

Archaeology of RNA polymerase: factor swapping during the transcription cycle.

机构信息

RNAP laboratory, University College London, Institute of Structural and Molecular Biology, Division of Biosciences, Gower Street, London WC1E 6BT, UK.

出版信息

Biochem Soc Trans. 2013 Feb 1;41(1):362-7. doi: 10.1042/BST20120274.

Abstract

All RNAPs (RNA polymerases) repeatedly make use of their DNA template by progressing through the transcription cycle multiple times. During transcription initiation and elongation, distinct sets of transcription factors associate with multisubunit RNAPs and modulate their nucleic-acid-binding and catalytic properties. Between the initiation and elongation phases of the cycle, the factors have to be exchanged by a largely unknown mechanism. We have shown that the binding sites for initiation and elongation factors are overlapping and that the binding of the factors to RNAP is mutually exclusive. This ensures an efficient exchange or 'swapping' of factors and could furthermore assist RNAP during promoter escape, enabling robust transcription. A similar mechanism applies to the bacterial RNAP system. The elongation factors are evolutionarily conserved between the bacterial (NusG) and archaeo-eukaryotic (Spt5) systems; however, the initiation factors [σ and TBP (TATA-box-binding protein)/TF (transcription factor) B respectively] are not. Therefore we propose that this factor-swapping mechanism, operating in all three domains of life, is the outcome of convergent evolution.

摘要

所有 RNA 聚合酶(RNAP)都通过多次通过转录循环来反复利用其 DNA 模板。在转录起始和延伸过程中,不同的转录因子与多亚基 RNAP 结合,并调节其核酸结合和催化特性。在循环的起始和延伸阶段之间,必须通过一种很大程度上未知的机制来交换这些因子。我们已经表明,起始和延伸因子的结合位点是重叠的,并且因子与 RNAP 的结合是相互排斥的。这确保了因子的有效交换或“交换”,并且可以在启动子逃逸期间进一步协助 RNAP,从而实现稳健的转录。类似的机制适用于细菌 RNAP 系统。延伸因子在细菌(NusG)和古真核(Spt5)系统之间是进化保守的;然而,起始因子[σ和 TBP(TATA 盒结合蛋白)/TF(转录因子)B 分别]则不是。因此,我们提出,这种在所有三个生命领域中起作用的因子交换机制是趋同进化的结果。

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