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Skalska, L.* ; Begley, V.* ; Beltran, M.* ; Lukauskas, S. ; Khandelwal, G.* ; Faull, P.* ; Bhamra, A.* ; Tavares, M.* ; Wellman, R.* ; Tvardovskiy, A. ; Foster, B. ; Ruiz de Los Mozos, I.* ; Herrero, J.* ; Surinova, S.* ; Snijders, A.P.* ; Bartke, T. ; Jenner, R.G.*

Nascent RNA antagonizes the interaction of a set of regulatory proteins with chromatin.

Mol. Cell 81, 2944-2959.e10 (2021)
Verlagsversion DOI PMC
Closed
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
A number of regulatory factors are recruited to chromatin by specialized RNAs. Whether RNA has a more general role in regulating the interaction of proteins with chromatin has not been determined. We used proteomics methods to measure the global impact of nascent RNA on chromatin in embryonic stem cells. Surprisingly, we found that nascent RNA primarily antagonized the interaction of chromatin modifiers and transcriptional regulators with chromatin. Transcriptional inhibition and RNA degradation induced recruitment of a set of transcriptional regulators, chromatin modifiers, nucleosome remodelers, and regulators of higher-order structure. RNA directly bound to factors, including BAF, NuRD, EHMT1, and INO80 and inhibited their interaction with nucleosomes. The transcriptional elongation factor P-TEFb directly bound pre-mRNA, and its recruitment to chromatin upon Pol II inhibition was regulated by the 7SK ribonucleoprotein complex. We postulate that by antagonizing the interaction of regulatory proteins with chromatin, nascent RNA links transcriptional output with chromatin composition.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Rna Polymerase Ii ; Rnase ; Chromatin ; Histone Modification ; Nascent Rna ; Nucleosome ; Nucleosome Remodeller ; Pre-mrna ; Transcription Factor ; Transcriptional Elongation; Repressive Complex 2; Polymerase-ii; P-tefb; Pervasive Transcription; Binding Protein; Snrnp Complex; Web Server; 7sk Snrnp; Hiv-1 Tat; Gene
Sprache englisch
Veröffentlichungsjahr 2021
HGF-Berichtsjahr 2021
ISSN (print) / ISBN 1097-2765
e-ISSN 1097-4164
Zeitschrift Molecular Cell
Quellenangaben Band: 81, Heft: 14, Seiten: 2944-2959.e10 Artikelnummer: , Supplement: ,
Verlag Elsevier
Verlagsort 50 Hampshire St, Floor 5, Cambridge, Ma 02139 Usa
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Functional Epigenetics (IFE)
POF Topic(s) 30203 - Molecular Targets and Therapies
Forschungsfeld(er) Helmholtz Diabetes Center
PSP-Element(e) G-502800-001
Förderungen Helmholtz Society
ERC
Worldwide Cancer Research
Blood Cancer UK
European Research Council (ERC)
Cancer Research UK Cancer Immunotherapy Network Accelerator (CITA)
Proteomics Research TTP - Cancer Research UK-UCL Centre
UCL Bill Lyons Informatics Centre - Cancer Research UK-UCL Centre
UCL Cancer Institute Genomics TTP
DOI 10.1016/j.molcel.2021.05.026
WOS ID WOS:000674644300009
PubMed ID 34166609
Erfassungsdatum 2021-07-22
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