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CDK9 and PP2A regulate RNA polymerase II transcription termination and coupled RNA maturation

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posted on 2024-07-10, 14:22 authored by Michael Tellier, Justyna Zaborowska, Jonathan Neve, Takayuki Nojima, Svenja Hester, Marjorie Fournier, Andre Furger, Shona Murphy

 CDK9 is a kinase critical for the productive transcription of protein‐coding genes by RNA polymerase II (pol II). As part of P‐TEFb, CDK9 phosphorylates the carboxyl‐terminal domain (CTD) of pol II and elongation factors, which allows pol II to elongate past the early elongation checkpoint (EEC) encountered soon after initiation. We show that, in addition to halting pol II at the EEC, loss of CDK9 activity causes premature termination of transcription across the last exon, loss of polyadenylation factors from chromatin, and loss of polyadenylation of nascent transcripts. Inhibition of the phosphatase PP2A abrogates the premature termination and loss of polyadenylation caused by CDK9 inhibition, indicating that this kinase/phosphatase pair regulates transcription elongation and RNA processing at the end of protein‐coding genes. We also confirm the splicing factor SF3B1 as a target of CDK9 and show that SF3B1 in complex with polyadenylation factors is lost from chromatin after CDK9 inhibition. These results emphasize the important roles that CDK9 plays in coupling transcription elongation and termination to RNA maturation downstream of the EEC. 

Funding

Wellcome Trust Investigator Award

The human pol II-transcribed snRNA genes; a model for gene-type specific transcription.

Biotechnology and Biological Sciences Research Council

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Regulation of gene expression by mechanisms that target alternatively cleaved and polyadenylated mRNA isoforms

Biotechnology and Biological Sciences Research Council

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MRC Studentship

History

Version

  • VoR (Version of Record)

Published in

EMBO reports

Volume

23

Issue

10

Publisher

EMBO

issn

1469-221X

eissn

1469-3178

Acceptance date

2022-07-21

Copyright date

2022

Available date

2024-07-10

Language

en

Data Access Statement

Sequencing data have been deposited in GEO under accession code GSE176541 (http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE176541). The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE (Perez‐Riverol et al, 2019) partner repository with the dataset identifier PXD026720 (SILAC) (http://www.ebi.ac.uk/pride/archive/projects/PXD026720) and PXD033694 (SF3B1) (http://www.ebi.ac.uk/pride/archive/projects/PXD033694). All data generated or analyzed during this study are included in the manuscript and supporting files. We include full excel spreadsheets representing original mass spectrometry data.

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