Department of Medicine, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0640, USA.
Department of Medicine, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0640, USA.
Cell. 2018 Sep 6;174(6):1522-1536.e22. doi: 10.1016/j.cell.2018.07.047. Epub 2018 Aug 23.
How transcription affects genome 3D organization is not well understood. We found that during influenza A (IAV) infection, rampant transcription rapidly reorganizes host cell chromatin interactions. These changes occur at the ends of highly transcribed genes, where global inhibition of transcription termination by IAV NS1 protein causes readthrough transcription for hundreds of kilobases. In these readthrough regions, elongating RNA polymerase II disrupts chromatin interactions by inducing cohesin displacement from CTCF sites, leading to locus decompaction. Readthrough transcription into heterochromatin regions switches them from the inert (B) to the permissive (A) chromatin compartment and enables transcription factor binding. Data from non-viral transcription stimuli show that transcription similarly affects cohesin-mediated chromatin contacts within gene bodies. Conversely, inhibition of transcription elongation allows cohesin to accumulate at previously transcribed intragenic CTCF sites and to mediate chromatin looping and compaction. Our data indicate that transcription elongation by RNA polymerase II remodels genome 3D architecture.
转录如何影响基因组 3D 组织尚不清楚。我们发现,在甲型流感(IAV)感染期间,猖獗的转录迅速重组宿主细胞染色质相互作用。这些变化发生在转录高度活跃的基因末端,IAV NS1 蛋白全局抑制转录终止导致数百千碱基的通读转录。在这些通读区域,延伸的 RNA 聚合酶 II 通过诱导黏连蛋白从 CTCF 位点位移,破坏染色质相互作用,导致基因座解压缩。通读转录进入异染色质区域会将它们从惰性(B)状态转换为允许(A)状态的染色质区室,并允许转录因子结合。来自非病毒转录刺激的数据表明,转录同样会影响基因体内黏连蛋白介导的染色质接触。相反,抑制转录延伸可使黏连蛋白在先前转录的基因内 CTCF 位点积累,并介导染色质环化和压缩。我们的数据表明,RNA 聚合酶 II 的转录延伸重塑了基因组 3D 结构。