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作为预防共转录R环范例的THO复合物

The THO Complex as a Paradigm for the Prevention of Cotranscriptional R-Loops.

作者信息

Luna Rosa, Rondón Ana G, Pérez-Calero Carmen, Salas-Armenteros Irene, Aguilera Andrés

机构信息

Centro Andaluz de Biología Molecular y Medicina Regenerativa CABIMER, Universidad de Sevilla-CSIC-Universidad Pablo de Olavide, 41092 Seville, Spain.

出版信息

Cold Spring Harb Symp Quant Biol. 2019;84:105-114. doi: 10.1101/sqb.2019.84.039594. Epub 2020 Jun 3.

Abstract

Different proteins associate with the nascent RNA and the RNA polymerase (RNAP) to catalyze the transcription cycle and RNA export. If these processes are not properly controlled, the nascent RNA can thread back and hybridize to the DNA template forming R-loops capable of stalling replication, leading to DNA breaks. Given the transcriptional promiscuity of the genome, which leads to large amounts of RNAs from mRNAs to different types of ncRNAs, these can become a major threat to genome integrity if they form R-loops. Consequently, cells have evolved nuclear factors to prevent this phenomenon that includes THO, a conserved eukaryotic complex acting in transcription elongation and RNA processing and export that upon inactivation causes genome instability linked to R-loop accumulation. We revise and discuss here the biological relevance of THO and a number of RNA helicases, including the THO partner UAP56/DDX39B, as a paradigm of the cellular mechanisms of cotranscriptional R-loop prevention.

摘要

不同的蛋白质与新生RNA和RNA聚合酶(RNAP)结合,以催化转录周期和RNA输出。如果这些过程没有得到适当控制,新生RNA可能会反向延伸并与DNA模板杂交,形成能够使复制停滞的R环,导致DNA断裂。鉴于基因组的转录混杂性,这会导致从mRNA到不同类型非编码RNA产生大量RNA,如果它们形成R环,这些RNA可能会对基因组完整性构成重大威胁。因此,细胞进化出了核因子来防止这种现象,其中包括THO,这是一种保守的真核复合物,作用于转录延伸、RNA加工和输出,失活后会导致与R环积累相关的基因组不稳定。我们在此修订并讨论THO和一些RNA解旋酶的生物学相关性,包括THO伴侣UAP56/DDX39B,作为共转录R环预防细胞机制的一个范例。

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