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The Paf1 Complex: A Keystone of Nuclear Regulation Operating at the Interface of Transcription and Chromatin

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JOURNAL OF MOLECULAR BIOLOGY
卷 433, 期 14, 页码 -

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ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jmb.2021.166979

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资金

  1. NIH [R01 GM052593]
  2. NSF Graduate Research Fellowship
  3. NIH fellowship [T32 GM133353]

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The regulation of transcription by RNA polymerase II is closely linked to the regulation of chromatin structure, with the Paf1C complex playing a crucial role in controlling transcription elongation, epigenetic modifications, and post-transcriptional steps. Recent studies have provided new insights into the mechanisms of Paf1C function, supported by high-resolution structural information, highlighting its broad impact on eukaryotic gene expression and nuclear regulation.
The regulation of transcription by RNA polymerase II is closely intertwined with the regulation of chromatin structure. A host of proteins required for the disassembly, reassembly, and modification of nucleosomes interacts with Pol II to aid its movement and counteract its disruptive effects on chromatin. The highly conserved Polymerase Associated Factor 1 Complex, Paf1C, travels with Pol II and exerts control over transcription elongation and chromatin structure, while broadly impacting the transcriptome in both single cell and multicellular eukaryotes. Recent studies have yielded exciting new insights into the mechanisms by which Paf1C regulates transcription elongation, epigenetic modifications, and post-transcriptional steps in eukaryotic gene expression. Importantly, these functional studies are now supported by an extensive foundation of high-resolution structural information, providing intimate views of Paf1C and its integration into the larger Pol II elongation complex. As a global regulatory factor operating at the interface between chromatin and transcription, the impact of Paf1C is broad and its influence reverberates into other domains of nuclear regulation, including genome stability, telomere maintenance, and DNA replication. (C) 2021 Elsevier Ltd. All rights reserved.

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