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The Cdk8 kinase module regulates interaction of the mediator complex with RNA polymerase II
The Cdk8 kinase module (CKM) is a dissociable part of the coactivator complex mediator, which regulates gene transcription by RNA polymerase II. The CKM has both negative and positive functions in gene transcription that remain poorly understood at the mechanistic level. In order to reconstitute the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191332/ https://www.ncbi.nlm.nih.gov/pubmed/33933450 http://dx.doi.org/10.1016/j.jbc.2021.100734 |
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author | Osman, Sara Mohammad, Eusra Lidschreiber, Michael Stuetzer, Alexandra Bazsó, Fanni Laura Maier, Kerstin C. Urlaub, Henning Cramer, Patrick |
author_facet | Osman, Sara Mohammad, Eusra Lidschreiber, Michael Stuetzer, Alexandra Bazsó, Fanni Laura Maier, Kerstin C. Urlaub, Henning Cramer, Patrick |
author_sort | Osman, Sara |
collection | PubMed |
description | The Cdk8 kinase module (CKM) is a dissociable part of the coactivator complex mediator, which regulates gene transcription by RNA polymerase II. The CKM has both negative and positive functions in gene transcription that remain poorly understood at the mechanistic level. In order to reconstitute the role of the CKM in transcription initiation, we prepared recombinant CKM from the yeast Saccharomyces cerevisiae. We showed that CKM bound to the core mediator (cMed) complex, sterically inhibiting cMed from binding to the polymerase II preinitiation complex (PIC) in vitro. We further showed that the Cdk8 kinase activity of the CKM weakened CKM–cMed interaction, thereby facilitating dissociation of the CKM and enabling mediator to bind the PIC in order to stimulate transcription initiation. Finally, we report that the kinase activity of Cdk8 is required for gene activation during the stressful condition of heat shock in vivo but not under steady-state growth conditions. Based on these results, we propose a model in which the CKM negatively regulates mediator function at upstream-activating sequences by preventing mediator binding to the PIC at the gene promoter. However, during gene activation in response to stress, the Cdk8 kinase activity of the CKM may release mediator and allow its binding to the PIC, thereby accounting for the positive function of CKM. This may impart improved adaptability to stress by allowing a rapid transcriptional response to environmental changes, and we speculate that a similar mechanism in metazoans may allow the precise timing of developmental transcription programs. |
format | Online Article Text |
id | pubmed-8191332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-81913322021-06-16 The Cdk8 kinase module regulates interaction of the mediator complex with RNA polymerase II Osman, Sara Mohammad, Eusra Lidschreiber, Michael Stuetzer, Alexandra Bazsó, Fanni Laura Maier, Kerstin C. Urlaub, Henning Cramer, Patrick J Biol Chem Research Article The Cdk8 kinase module (CKM) is a dissociable part of the coactivator complex mediator, which regulates gene transcription by RNA polymerase II. The CKM has both negative and positive functions in gene transcription that remain poorly understood at the mechanistic level. In order to reconstitute the role of the CKM in transcription initiation, we prepared recombinant CKM from the yeast Saccharomyces cerevisiae. We showed that CKM bound to the core mediator (cMed) complex, sterically inhibiting cMed from binding to the polymerase II preinitiation complex (PIC) in vitro. We further showed that the Cdk8 kinase activity of the CKM weakened CKM–cMed interaction, thereby facilitating dissociation of the CKM and enabling mediator to bind the PIC in order to stimulate transcription initiation. Finally, we report that the kinase activity of Cdk8 is required for gene activation during the stressful condition of heat shock in vivo but not under steady-state growth conditions. Based on these results, we propose a model in which the CKM negatively regulates mediator function at upstream-activating sequences by preventing mediator binding to the PIC at the gene promoter. However, during gene activation in response to stress, the Cdk8 kinase activity of the CKM may release mediator and allow its binding to the PIC, thereby accounting for the positive function of CKM. This may impart improved adaptability to stress by allowing a rapid transcriptional response to environmental changes, and we speculate that a similar mechanism in metazoans may allow the precise timing of developmental transcription programs. American Society for Biochemistry and Molecular Biology 2021-04-30 /pmc/articles/PMC8191332/ /pubmed/33933450 http://dx.doi.org/10.1016/j.jbc.2021.100734 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Osman, Sara Mohammad, Eusra Lidschreiber, Michael Stuetzer, Alexandra Bazsó, Fanni Laura Maier, Kerstin C. Urlaub, Henning Cramer, Patrick The Cdk8 kinase module regulates interaction of the mediator complex with RNA polymerase II |
title | The Cdk8 kinase module regulates interaction of the mediator complex with RNA polymerase II |
title_full | The Cdk8 kinase module regulates interaction of the mediator complex with RNA polymerase II |
title_fullStr | The Cdk8 kinase module regulates interaction of the mediator complex with RNA polymerase II |
title_full_unstemmed | The Cdk8 kinase module regulates interaction of the mediator complex with RNA polymerase II |
title_short | The Cdk8 kinase module regulates interaction of the mediator complex with RNA polymerase II |
title_sort | cdk8 kinase module regulates interaction of the mediator complex with rna polymerase ii |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191332/ https://www.ncbi.nlm.nih.gov/pubmed/33933450 http://dx.doi.org/10.1016/j.jbc.2021.100734 |
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