PP1/PNUTS phosphatase binds the restrictor complex and stimulates RNA Pol II transcription termination

The restrictor ZC3H4/WDR82 terminates antisense transcription from bidirectional promoters, but its mechanism is poorly understood. We report that ZC3H4/WDR82 immunoprecipitates with PP1 phosphatase and its nuclear targeting subunit, PP1 phosphatase nuclear targeting subunit (PNUTS), which binds to WDR82. AlphaFold predicts a complex of PP1/PNUTS with the restrictor where both PNUTS and ZC3H4 contact WDR82. A substrate trap, PP1<sup>H66K</sup>-PNUTS, comprising inactive PP1 fused to the PNUTS C terminus, antagonizes restrictor-mediated termination, whereas PP1<sup>WT</sup>-PNUTS has less of an effect, suggesting that phosphatase activity is required for termination. One PP1/PNUTS substrate implicated in termination by the restrictor is RNA polymerase II (RNA Pol II) CTD Ser5-P. PP1<sup>H66K</sup>-PNUTS induces Ser5-P hyperphosphorylation at 5' ends, presumably by inhibiting dephosphorylation. NET-seq analysis suggests that CTD Ser5 dephosphorylation would promote termination by increasing RNA Pol II pausing. Both inhibition of termination and CTD hyperphosphorylation require the WDR82 binding domain of PP1<sup>H66K</sup>-PNUTS, which mediates restrictor binding. In summary, the PP1/PNUTS phosphatase associated with the restrictor via WDR82 promotes efficient transcription termination.

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Publication Details

Journal
Cell Reports
Published
2025-04-16
DOI
https://doi.org/10.1016/j.celrep.2025.115564
Citations
4
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
3.22
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article

PP1/PNUTS phosphatase binds the restrictor complex and stimulates RNA Pol II transcription termination

Stéphane Mouilleron, Ryan M. Sheridan, David L. Bentley, Benjamin Erickson et al.
4 citations
Cell Reports
RNA modifications and cancer
3.22
article

PP1/PNUTS phosphatase binds the restrictor complex and stimulates RNA Pol II transcription termination

Stéphane Mouilleron, Ryan M. Sheridan, David L. Bentley, Benjamin Erickson, Nova Fong, Richard Treisman, Roman O Fedoryshchak, Kirk C. Hansen, Anthony J. Saviola, Keira Y. Larson
article en
4 citations

Abstract

The restrictor ZC3H4/WDR82 terminates antisense transcription from bidirectional promoters, but its mechanism is poorly understood. We report that ZC3H4/WDR82 immunoprecipitates with PP1 phosphatase and its nuclear targeting subunit, PP1 phosphatase nuclear targeting subunit (PNUTS), which binds to WDR82. AlphaFold predicts a complex of PP1/PNUTS with the restrictor where both PNUTS and ZC3H4 contact WDR82. A substrate trap, PP1<sup>H66K</sup>-PNUTS, comprising inactive PP1 fused to the PNUTS C terminus, antagonizes restrictor-mediated termination, whereas PP1<sup>WT</sup>-PNUTS has less of an effect, suggesting that phosphatase activity is required for termination. One PP1/PNUTS substrate implicated in termination by the restrictor is RNA polymerase II (RNA Pol II) CTD Ser5-P. PP1<sup>H66K</sup>-PNUTS induces Ser5-P hyperphosphorylation at 5' ends, presumably by inhibiting dephosphorylation. NET-seq analysis suggests that CTD Ser5 dephosphorylation would promote termination by increasing RNA Pol II pausing. Both inhibition of termination and CTD hyperphosphorylation require the WDR82 binding domain of PP1<sup>H66K</sup>-PNUTS, which mediates restrictor binding. In summary, the PP1/PNUTS phosphatase associated with the restrictor via WDR82 promotes efficient transcription termination.

Cell ReportsVol. 44(5)
The Francis Crick Institute (GB), University of Colorado Anschutz Medical Campus (US), University of Colorado Denver (US)
Zero hunger
Openalex Percentile: Top 9%
RNA modifications and cancer
3.22
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