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Tyrosine phosphorylation of RNA polymerase II CTD is associated with antisense promoter transcription and active enhancers in mammalian cells
In mammals, the carboxy-terminal domain (CTD) of RNA polymerase (Pol) II consists of 52 conserved heptapeptide repeats containing the consensus sequence Tyr1-Ser2-Pro3-Thr4-Ser5-Pro6-Ser7. Post-translational modifications of the CTD coordinate the transcription cycle and various steps of mRNA matura...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042876/ https://www.ncbi.nlm.nih.gov/pubmed/24842994 http://dx.doi.org/10.7554/eLife.02105 |
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author | Descostes, Nicolas Heidemann, Martin Spinelli, Lionel Schüller, Roland Maqbool, Muhammad Ahmad Fenouil, Romain Koch, Frederic Innocenti, Charlène Gut, Marta Gut, Ivo Eick, Dirk Andrau, Jean-Christophe |
author_facet | Descostes, Nicolas Heidemann, Martin Spinelli, Lionel Schüller, Roland Maqbool, Muhammad Ahmad Fenouil, Romain Koch, Frederic Innocenti, Charlène Gut, Marta Gut, Ivo Eick, Dirk Andrau, Jean-Christophe |
author_sort | Descostes, Nicolas |
collection | PubMed |
description | In mammals, the carboxy-terminal domain (CTD) of RNA polymerase (Pol) II consists of 52 conserved heptapeptide repeats containing the consensus sequence Tyr1-Ser2-Pro3-Thr4-Ser5-Pro6-Ser7. Post-translational modifications of the CTD coordinate the transcription cycle and various steps of mRNA maturation. Here we describe Tyr1 phosphorylation (Tyr1P) as a hallmark of promoter (5′ associated) Pol II in mammalian cells, in contrast to what was described in yeast. Tyr1P is predominantly found in antisense orientation at promoters but is also specifically enriched at active enhancers. Mutation of Tyr1 to phenylalanine (Y1F) prevents the formation of the hyper-phosphorylated Pol IIO form, induces degradation of Pol II to the truncated Pol IIB form, and results in a lethal phenotype. Our results suggest that Tyr1P has evolved specialized and essential functions in higher eukaryotes associated with antisense promoter and enhancer transcription, and Pol II stability. DOI: http://dx.doi.org/10.7554/eLife.02105.001 |
format | Online Article Text |
id | pubmed-4042876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40428762014-06-16 Tyrosine phosphorylation of RNA polymerase II CTD is associated with antisense promoter transcription and active enhancers in mammalian cells Descostes, Nicolas Heidemann, Martin Spinelli, Lionel Schüller, Roland Maqbool, Muhammad Ahmad Fenouil, Romain Koch, Frederic Innocenti, Charlène Gut, Marta Gut, Ivo Eick, Dirk Andrau, Jean-Christophe eLife Genes and Chromosomes In mammals, the carboxy-terminal domain (CTD) of RNA polymerase (Pol) II consists of 52 conserved heptapeptide repeats containing the consensus sequence Tyr1-Ser2-Pro3-Thr4-Ser5-Pro6-Ser7. Post-translational modifications of the CTD coordinate the transcription cycle and various steps of mRNA maturation. Here we describe Tyr1 phosphorylation (Tyr1P) as a hallmark of promoter (5′ associated) Pol II in mammalian cells, in contrast to what was described in yeast. Tyr1P is predominantly found in antisense orientation at promoters but is also specifically enriched at active enhancers. Mutation of Tyr1 to phenylalanine (Y1F) prevents the formation of the hyper-phosphorylated Pol IIO form, induces degradation of Pol II to the truncated Pol IIB form, and results in a lethal phenotype. Our results suggest that Tyr1P has evolved specialized and essential functions in higher eukaryotes associated with antisense promoter and enhancer transcription, and Pol II stability. DOI: http://dx.doi.org/10.7554/eLife.02105.001 eLife Sciences Publications, Ltd 2014-05-09 /pmc/articles/PMC4042876/ /pubmed/24842994 http://dx.doi.org/10.7554/eLife.02105 Text en Copyright © 2014, Descostes et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genes and Chromosomes Descostes, Nicolas Heidemann, Martin Spinelli, Lionel Schüller, Roland Maqbool, Muhammad Ahmad Fenouil, Romain Koch, Frederic Innocenti, Charlène Gut, Marta Gut, Ivo Eick, Dirk Andrau, Jean-Christophe Tyrosine phosphorylation of RNA polymerase II CTD is associated with antisense promoter transcription and active enhancers in mammalian cells |
title | Tyrosine phosphorylation of RNA polymerase II CTD is associated with antisense promoter transcription and active enhancers in mammalian cells |
title_full | Tyrosine phosphorylation of RNA polymerase II CTD is associated with antisense promoter transcription and active enhancers in mammalian cells |
title_fullStr | Tyrosine phosphorylation of RNA polymerase II CTD is associated with antisense promoter transcription and active enhancers in mammalian cells |
title_full_unstemmed | Tyrosine phosphorylation of RNA polymerase II CTD is associated with antisense promoter transcription and active enhancers in mammalian cells |
title_short | Tyrosine phosphorylation of RNA polymerase II CTD is associated with antisense promoter transcription and active enhancers in mammalian cells |
title_sort | tyrosine phosphorylation of rna polymerase ii ctd is associated with antisense promoter transcription and active enhancers in mammalian cells |
topic | Genes and Chromosomes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042876/ https://www.ncbi.nlm.nih.gov/pubmed/24842994 http://dx.doi.org/10.7554/eLife.02105 |
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