Suna In, Patricia Renck Nunes, Rita Valador Fernandes, Joachim Lingner
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引用次数: 0
摘要
TERRA长非编码rna通过与端粒DNA碱基配对形成r环结构与端粒转录后相关。TERRA调节端粒维持,但其确切的作用模式尚不清楚。本研究在端粒酶表达细胞中诱导TERRA转录和r环形成,并确定TERRA r环的形成需要RAD51 DNA重组酶及其增强子RAD51AP1的非冗余功能。TERRA r -环干扰半保守性DNA复制,通过称为断裂诱导复制(BIR)的同源定向修复(HDR)机制促进端粒维持,从而确保ALT癌细胞的端粒维持。此外,TERRA诱导primpol依赖的修复,这可以在复制障碍的下游启动DNA合成。PRIMPOL与BIR平行作用于terra过表达细胞的端粒维持,促进其存活。同样,我们发现在U2OS ALT癌细胞中,PRIMPOL缺失与BIR缺失是合成致死的。因此,在没有其他alt -典型端粒染色质变化的情况下,TERRA r -环本身足以诱导alt -典型端粒修复机制。
TERRA R-loops trigger a switch in telomere maintenance towards break-induced replication and PRIMPOL-dependent repair.
TERRA long noncoding RNAs associate with telomeres post transcription through base-pairing with telomeric DNA forming R-loop structures. TERRA regulates telomere maintenance but its exact modes of action remain unknown. Here, we induce TERRA transcription and R-loop formation in telomerase-expressing cells and determine that TERRA R-loop formation requires non-redundant functions of the RAD51 DNA recombinase and its enhancer RAD51AP1. TERRA R-loops interfere with semiconservative DNA replication, promoting telomere maintenance by a homology-directed repair (HDR) mechanism known as break-induced replication (BIR), which ensures telomere maintenance in ALT cancer cells. In addition, TERRA induces PRIMPOL-dependent repair, which can initiate DNA synthesis de novo downstream of replication obstacles. PRIMPOL acts in parallel to BIR for telomere maintenance of TERRA-overexpressing cells, promoting their survival. Similarly, we find that PRIMPOL depletion is synthetic-lethal with BIR deficiency in U2OS ALT cancer cells. Therefore, TERRA R-loops by themselves are sufficient to induce ALT-typical telomere repair mechanisms, in the absence of other ALT-typical telomeric chromatin changes.
期刊介绍:
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