Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Univ. Paris-Sud, Université Paris-Saclay, 91198, Gif-sur-Yvette cedex, France.
CEA, CNRGH, LGF, Genopole G2, 91057, Evry cedex, France.
Nucleic Acids Res. 2019 Sep 26;47(17):8988-9004. doi: 10.1093/nar/gkz598.
Transcription and maintenance of genome integrity are fundamental cellular functions. Deregulation of transcription and defects in DNA repair lead to serious pathologies. The Mediator complex links RNA polymerase (Pol) II transcription and nucleotide excision repair via Rad2/XPG endonuclease. However, the functional interplay between Rad2/XPG, Mediator and Pol II remains to be determined. In this study, we investigated their functional dynamics using genomic and genetic approaches. In a mutant affected in Pol II phosphorylation leading to Mediator stabilization on core promoters, Rad2 genome-wide occupancy shifts towards core promoters following that of Mediator, but decreases on transcribed regions together with Pol II. Specific Mediator mutations increase UV sensitivity, reduce Rad2 recruitment to transcribed regions, lead to uncoupling of Rad2, Mediator and Pol II and to colethality with deletion of Rpb9 Pol II subunit involved in transcription-coupled repair. We provide new insights into the functional interplay between Rad2, Mediator and Pol II and propose that dynamic interactions with Mediator and Pol II are involved in Rad2 loading to the chromatin. Our work contributes to the understanding of the complex link between transcription and DNA repair machineries, dysfunction of which leads to severe diseases.
转录和基因组完整性的维持是细胞的基本功能。转录失调和 DNA 修复缺陷会导致严重的病理。中介复合物通过 Rad2/XPG 内切酶将 RNA 聚合酶 (Pol) II 转录和核苷酸切除修复联系起来。然而,Rad2/XPG、中介复合物和 Pol II 之间的功能相互作用仍有待确定。在这项研究中,我们使用基因组和遗传方法研究了它们的功能动态。在一个影响 Pol II 磷酸化导致中介复合物在核心启动子上稳定的突变体中,Rad2 的全基因组占有率在中介复合物之后向核心启动子转移,但在转录区域与 Pol II 一起减少。特定的中介复合物突变增加了 UV 敏感性,减少了 Rad2 在转录区域的募集,导致 Rad2、中介复合物和 Pol II 解偶联,并与参与转录偶联修复的 Rpb9 Pol II 亚基缺失致死。我们提供了 Rad2、中介复合物和 Pol II 之间功能相互作用的新见解,并提出与中介复合物和 Pol II 的动态相互作用涉及 Rad2 向染色质的加载。我们的工作有助于理解转录和 DNA 修复机制之间复杂的联系,这些机制的功能障碍会导致严重的疾病。