| Literature DB >> 30146161 |
Sven Heinz1, Lorane Texari2, Michael G B Hayes2, Matthew Urbanowski3, Max W Chang2, Ninvita Givarkes2, Alexander Rialdi3, Kris M White3, Randy A Albrecht4, Lars Pache5, Ivan Marazzi4, Adolfo García-Sastre6, Megan L Shaw3, Christopher Benner7.
Abstract
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.Entities:
Keywords: CTCF; NS1; chromatin compaction; cohesin; genome 3D structure; influenza A virus; readthrough transcription; transcription; transcription elongation; transcription termination
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Year: 2018 PMID: 30146161 PMCID: PMC6130916 DOI: 10.1016/j.cell.2018.07.047
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582