| Literature DB >> 36206739 |
Nova Fong1, Ryan M Sheridan1, Srinivas Ramachandran1, David L Bentley2.
Abstract
The pause-release model of transcription proposes that 40-100 bases from the start site RNA Pol II pauses, followed by release into productive elongation. Pause release is facilitated by the PTEFb phosphorylation of the RNA Pol II elongation factor, Spt5. We mapped paused polymerases by eNET-seq and found frequent pausing in zones that extend ∼0.3-3 kb into genes even when PTEFb is inhibited. The fraction of paused polymerases or pausing propensity declines gradually over several kb and not abruptly as predicted for a discrete pause-release event. Spt5 depletion extends pausing zones, suggesting that it promotes the maturation of elongation complexes to a low-pausing state. The expression of mutants after Spt5 depletion showed that phosphomimetic substitutions in the CTR1 domain diminished pausing throughout genes. By contrast, mutants that prevent the phosphorylation of the Spt5 RNA-binding domain strengthened pausing. Thus, distinct Spt5 phospho-isoforms set the balance between pausing and elongation.Entities:
Keywords: DRB; NET-seq; Spt5; Spt5 phosphorylation; pause-release model; transcription elongation; transcriptional pausing
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Year: 2022 PMID: 36206739 PMCID: PMC9555879 DOI: 10.1016/j.molcel.2022.09.001
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 19.328