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

Rosa Luna, Ana G Rondón, Carmen Pérez-Calero, Irene Salas-Armenteros, Andrés Aguilera
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引用次数: 24

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.

THO复合体是防止共转录r环的范例。
不同的蛋白质与新生RNA和RNA聚合酶(RNAP)结合,催化转录周期和RNA输出。如果这些过程没有得到适当的控制,新生的RNA可以返回并与DNA模板杂交,形成能够阻止复制的r环,导致DNA断裂。鉴于基因组的转录杂乱性,导致大量rna从mrna转化为不同类型的ncrna,如果它们形成r环,可能成为基因组完整性的主要威胁。因此,细胞已经进化出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体,在转录延伸和RNA加工和输出中起作用,失活后导致与r环积累相关的基因组不稳定。我们在此修订并讨论了THO和一些RNA解旋酶的生物学相关性,包括THO的合作伙伴UAP56/DDX39B,作为协同转录r环预防的细胞机制范例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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