Institut Curie, Centre de Recherche, Orsay, France; CNRS UMR3348, Genotoxic Stress and Cancer, Centre Universitaire, Orsay, France.
Institut Curie, Centre de Recherche, Orsay, France; CNRS UMR3348, Genotoxic Stress and Cancer, Centre Universitaire, Orsay, France.
Trends Biochem Sci. 2014 Mar;39(3):141-9. doi: 10.1016/j.tibs.2014.01.003. Epub 2014 Feb 14.
Recent work, including large-scale genetic and molecular analyses, identified RNA-binding proteins (RBPs) as major players in the prevention of genome instability. These studies show that RBPs prevent harmful RNA/DNA hybrids and are involved in the DNA damage response (DDR), from DNA repair to cell survival decisions. Indeed, specific RBPs allow the selective regulation of DDR genes at multiple post-transcriptional levels (from pre-mRNA splicing/polyadenylation to mRNA stability/translation) and are directly involved in DNA repair. These multiple activities are mediated by RBP binding to mRNAs, nascent transcripts, noncoding RNAs, and damaged DNA. Finally, because DNA damage modifies RBP localization and binding to different RNA/DNA molecules, we propose that upon DNA damage, RBPs coordinately regulate various aspects of both RNA and DNA metabolism.
最近的研究工作,包括大规模的遗传和分子分析,确定 RNA 结合蛋白(RBPs)是防止基因组不稳定性的主要因素。这些研究表明,RBPs 可以防止有害的 RNA/DNA 杂交,并参与 DNA 损伤反应(DDR),从 DNA 修复到细胞存活决策。事实上,特定的 RBPs 允许在多个转录后水平(从 pre-mRNA 剪接/多聚腺苷酸化到 mRNA 稳定性/翻译)选择性地调节 DDR 基因,并且直接参与 DNA 修复。这些多种活性是通过 RBP 与 mRNA、新生转录本、非编码 RNA 和受损 DNA 的结合来介导的。最后,因为 DNA 损伤改变了 RBP 与不同的 RNA/DNA 分子的定位和结合,我们提出,在 DNA 损伤后,RBPs 可以协调调节 RNA 和 DNA 代谢的各个方面。