| Literature DB >> 32229306 |
Charli B Fant1, Cecilia B Levandowski1, Kapil Gupta2, Zachary L Maas1, John Moir1, Jonathan D Rubin1, Andrew Sawyer3, Meagan N Esbin1, Jenna K Rimel1, Olivia Luyties1, Michael T Marr3, Imre Berger2, Robin D Dowell4, Dylan J Taatjes5.
Abstract
RNA polymerase II (RNAPII) transcription is governed by the pre-initiation complex (PIC), which contains TFIIA, TFIIB, TFIID, TFIIE, TFIIF, TFIIH, RNAPII, and Mediator. After initiation, RNAPII enzymes pause after transcribing less than 100 bases; precisely how RNAPII pausing is enforced and regulated remains unclear. To address specific mechanistic questions, we reconstituted human RNAPII promoter-proximal pausing in vitro, entirely with purified factors (no extracts). As expected, NELF and DSIF increased pausing, and P-TEFb promoted pause release. Unexpectedly, the PIC alone was sufficient to reconstitute pausing, suggesting RNAPII pausing is an inherent PIC function. In agreement, pausing was lost upon replacement of the TFIID complex with TATA-binding protein (TBP), and PRO-seq experiments revealed widespread disruption of RNAPII pausing upon acute depletion (t = 60 min) of TFIID subunits in human or Drosophila cells. These results establish a TFIID requirement for RNAPII pausing and suggest pause regulatory factors may function directly or indirectly through TFIID.Entities:
Keywords: DSIF; NELF; P-TEFb; PRO-seq; RNA polymerase II; TAF1; TBP; TFIID; TRIM-Away; pausing
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Year: 2020 PMID: 32229306 PMCID: PMC7245555 DOI: 10.1016/j.molcel.2020.03.008
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970