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检查点缺陷引发WRNIP1介导的反应以对抗R环相关的基因组不稳定。

Checkpoint Defects Elicit a WRNIP1-Mediated Response to Counteract R-Loop-Associated Genomic Instability.

作者信息

Marabitti Veronica, Lillo Giorgia, Malacaria Eva, Palermo Valentina, Pichierri Pietro, Franchitto Annapaola

机构信息

Department of Environment and Health, Section of Mechanisms Biomarkers and Models, Istituto Superiore di Sanita', Viale Regina Elena 299, 00161 Rome, Italy.

出版信息

Cancers (Basel). 2020 Feb 7;12(2):389. doi: 10.3390/cancers12020389.

Abstract

Conflicts between replication and transcription are a common source of genomic instability, a characteristic of almost all human cancers. Aberrant R-loops can cause a block to replication fork progression. A growing number of factors are involved in the resolution of these harmful structures and many perhaps are still unknown. Here, we reveal that the Werner interacting protein 1 (WRNIP1)-mediated response is implicated in counteracting aberrant R-loop accumulation. Using human cellular models with compromised Ataxia-Telangiectasia and Rad3-Related (ATR)-dependent checkpoint activation, we show that WRNIP1 is stabilized in chromatin and is needed for maintaining genome integrity by mediating the Ataxia Telangiectasia Mutated (ATM)-dependent phosphorylation of Checkpoint kinase 1 (CHK1). Furthermore, we demonstrated that loss of Werner Syndrome protein (WRN) or ATR signaling leads to formation of R-loop-dependent parental ssDNA upon mild replication stress, which is covered by Radiorestistance protein 51 (RAD51). We prove that Werner helicase-interacting protein 1 (WRNIP1) chromatin retention is also required to stabilize the association of RAD51 with ssDNA in proximity of R-loops. Therefore, in these pathological contexts, ATM inhibition or WRNIP1 abrogation is accompanied by increased levels of genomic instability. Overall, our findings suggest a novel function for WRNIP1 in preventing R-loop-driven genome instability, providing new clues to understand the way replication-transcription conflicts are handled.

摘要

复制与转录之间的冲突是基因组不稳定的常见来源,而基因组不稳定是几乎所有人类癌症的一个特征。异常的R环可导致复制叉前进受阻。越来越多的因素参与到这些有害结构的解决过程中,可能仍有许多因素未知。在此,我们揭示Werner相互作用蛋白1(WRNIP1)介导的反应与对抗异常R环积累有关。利用共济失调毛细血管扩张症和Rad3相关蛋白(ATR)依赖性检查点激活受损的人类细胞模型,我们发现WRNIP1在染色质中稳定存在,并且通过介导共济失调毛细血管扩张症突变蛋白(ATM)依赖性的检查点激酶1(CHK1)磷酸化来维持基因组完整性。此外,我们证明,在轻度复制应激下,Werner综合征蛋白(WRN)或ATR信号缺失会导致R环依赖性的亲本单链DNA形成,该单链DNA被耐辐射蛋白51(RAD51)覆盖。我们证明,在R环附近,WRNIP1在染色质中的保留对于稳定RAD51与单链DNA的结合也是必需的。因此,在这些病理情况下,ATM抑制或WRNIP1缺失会伴随着基因组不稳定性水平的增加。总体而言,我们的研究结果揭示了WRNIP1在预防R环驱动的基因组不稳定方面的新功能,为理解复制-转录冲突的处理方式提供了新线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b105/7072626/ebc3b8e5feb7/cancers-12-00389-g001.jpg

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