Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA.
Nat Rev Genet. 2018 Jun;19(6):385-397. doi: 10.1038/s41576-018-0001-6.
Proteotoxic stress, that is, stress caused by protein misfolding and aggregation, triggers the rapid and global reprogramming of transcription at genes and enhancers. Genome-wide assays that track transcriptionally engaged RNA polymerase II (Pol II) at nucleotide resolution have provided key insights into the underlying molecular mechanisms that regulate transcriptional responses to stress. In addition, recent kinetic analyses of transcriptional control under heat stress have shown how cells 'prewire' and rapidly execute genome-wide changes in transcription while concurrently becoming poised for recovery. The regulation of Pol II at genes and enhancers in response to heat stress is coupled to chromatin modification and compartmentalization, as well as to co-transcriptional RNA processing. These mechanistic features seem to apply broadly to other coordinated genome-regulatory responses.
蛋白质毒性应激,即由蛋白质错误折叠和聚集引起的应激,会触发基因和增强子上转录的快速和全局重编程。在核苷酸分辨率上跟踪转录相关 RNA 聚合酶 II(Pol II)的全基因组分析为调节应激转录反应的基础分子机制提供了重要的见解。此外,最近对热应激下转录控制的动力学分析表明,细胞如何“预先布线”并快速执行全基因组转录变化,同时为恢复做好准备。Pol II 在基因和增强子上对热应激的调节与染色质修饰和区室化以及共转录 RNA 加工相关。这些机制特征似乎广泛适用于其他协调的基因组调节反应。