RNA 裂解亚基 C11/RPC10 的进化以及 RNA 聚合酶 III 的循环。

Saurabh Mishra, Richard J Maraia
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引用次数: 0

摘要

核 RNA 聚合酶(Pol)III 通过一个独特的过程合成大量 tRNA 和其他短非编码 (nc)RNA,该过程涉及终止相关的再启动-再循环机制。除了其 17 个亚基中最大的两个有助于活性中心 RNA-DNA 结合和催化位点外,还有一个约 110 aa 的较小亚基(酵母 C11,人类 RPC10)监测该位点,可以改变其活性,并且对再启动-再循环至关重要。细胞质(细胞)Pol III 是富含 AT 的病毒 DNA 的直接传感器,它能合成 5'-ppp-RNA 信号分子,从而激活干扰素(IFN)的产生。编码 Pol III 亚基的基因发生突变会导致严重的抗病毒免疫缺陷,但细胞-Pol III 在富含 AT 的 DNA 上启动的机制尚不清楚。Cyto-Pol III 还与诱导 IFN 以应对自身免疫功能障碍中的细胞膜线粒体 DNA 有关。本评论的一个重点是最近的生化和遗传学研究,这些研究考察了 C11 的各个结构域在 Pol III 终止相关的重启-再循环过程中的作用,以及最近的低温电子显微镜结构和伴随分析,这些分析在进化和其他生物学背景下都得到了考虑。C11/RPC10 的 N 端结构域(NTD)锚定在 Pol III 的外围,一个高度保守的连接体从该结构域延伸到可移动的 C 端 RNA 切割结构域,该结构域可伸入活性中心并挽救停滞的复合体。生化数据表明,在转录周期中,NTD 和 CTD 的活动是可分离的,而 NTD-连接体可赋予 Pol III 在进化上独一无二的终止-重启-再循环活动。根据单颗粒低温电子显微镜构象建立的模型表明,C11-Linker-CTD 与最大亚基的 DNA 结合钳的异构运动协调,进出活性中心,将终止与再启动-再循环结合起来。这些可能与免疫信号传导过程中细胞-Pol III 的 DNA 负载有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evolution of the RNA Cleavage Subunit C11/RPC10, and Recycling by RNA Polymerase III.

Evolution of the RNA Cleavage Subunit C11/RPC10, and Recycling by RNA Polymerase III.

Nuclear RNA polymerase (Pol) III synthesizes large amounts of tRNAs and other short non-coding (nc)RNAs by a unique process that involves a termination-associated reinitiation-recycling mechanism. In addition to its two largest of 17 subunits, which contribute to active center RNA-DNA binding and catalytic site, a smaller subunit of ~110 aa (yeast C11, human RPC10) monitors this site, can modify its activity, and is essential for reinitiation-recycling. Distinct, but relevant to human immunity is cytoplasmic (cyto-)Pol III that is a direct sensor of AT-rich viral DNA from which it synthesizes 5'-ppp-RNA signaling molecules that activate interferon (IFN) production. Mutations in genes encoding Pol III subunits cause severe anti-viral immunodeficiency although the mechanisms responsible for cyto-Pol III initiation on this AT-rich DNA are unknown. Cyto-Pol III has also been implicated in inducing IFN in response to cytosolic mitochondrial DNA in autoimmune dysfunction. A focus of this commentary is recent biochemical and genetics research that examined the roles of the individual domains of C11 in the Pol III termination-associated reinitiation-recycling process as well as more recent cryo-EM structural and accompanying analyses, that are considered in evolutionary and other biological contexts. The N-terminal domain (NTD) of C11/RPC10 anchors at the periphery of Pol III from which a highly conserved linker extends to the mobile C-terminal RNA cleavage domain that can reach into the active center and rescue arrested complexes. Biochemical data indicate separable activities for the NTD and CTD in the transcription cycle, whereas the NTD-Linker can confer the evolutionary unique Pol III termination-reinitiation-recycling activity. A model produced from single particle cryo-EM conformations indicates that the C11-Linker-CTD swings in and out of the active center coordinated with allosteric movements of the DNA-binding clamp by the largest subunit, coupling termination to reinitiation-recycling. These may be relevant to DNA loading by cyto-Pol III during immune signaling.

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