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The SET1 Complex Selects Actively Transcribed Target Genes via Multivalent Interaction with CpG Island Chromatin
Chromatin modifications and the promoter-associated epigenome are important for the regulation of gene expression. However, the mechanisms by which chromatin-modifying complexes are targeted to the appropriate gene promoters in vertebrates and how they influence gene expression have remained poorly...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603731/ https://www.ncbi.nlm.nih.gov/pubmed/28877467 http://dx.doi.org/10.1016/j.celrep.2017.08.030 |
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author | Brown, David A. Di Cerbo, Vincenzo Feldmann, Angelika Ahn, Jaewoo Ito, Shinsuke Blackledge, Neil P. Nakayama, Manabu McClellan, Michael Dimitrova, Emilia Turberfield, Anne H. Long, Hannah K. King, Hamish W. Kriaucionis, Skirmantas Schermelleh, Lothar Kutateladze, Tatiana G. Koseki, Haruhiko Klose, Robert J. |
author_facet | Brown, David A. Di Cerbo, Vincenzo Feldmann, Angelika Ahn, Jaewoo Ito, Shinsuke Blackledge, Neil P. Nakayama, Manabu McClellan, Michael Dimitrova, Emilia Turberfield, Anne H. Long, Hannah K. King, Hamish W. Kriaucionis, Skirmantas Schermelleh, Lothar Kutateladze, Tatiana G. Koseki, Haruhiko Klose, Robert J. |
author_sort | Brown, David A. |
collection | PubMed |
description | Chromatin modifications and the promoter-associated epigenome are important for the regulation of gene expression. However, the mechanisms by which chromatin-modifying complexes are targeted to the appropriate gene promoters in vertebrates and how they influence gene expression have remained poorly defined. Here, using a combination of live-cell imaging and functional genomics, we discover that the vertebrate SET1 complex is targeted to actively transcribed gene promoters through CFP1, which engages in a form of multivalent chromatin reading that involves recognition of non-methylated DNA and histone H3 lysine 4 trimethylation (H3K4me3). CFP1 defines SET1 complex occupancy on chromatin, and its multivalent interactions are required for the SET1 complex to place H3K4me3. In the absence of CFP1, gene expression is perturbed, suggesting that normal targeting and function of the SET1 complex are central to creating an appropriately functioning vertebrate promoter-associated epigenome. |
format | Online Article Text |
id | pubmed-5603731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56037312017-10-12 The SET1 Complex Selects Actively Transcribed Target Genes via Multivalent Interaction with CpG Island Chromatin Brown, David A. Di Cerbo, Vincenzo Feldmann, Angelika Ahn, Jaewoo Ito, Shinsuke Blackledge, Neil P. Nakayama, Manabu McClellan, Michael Dimitrova, Emilia Turberfield, Anne H. Long, Hannah K. King, Hamish W. Kriaucionis, Skirmantas Schermelleh, Lothar Kutateladze, Tatiana G. Koseki, Haruhiko Klose, Robert J. Cell Rep Article Chromatin modifications and the promoter-associated epigenome are important for the regulation of gene expression. However, the mechanisms by which chromatin-modifying complexes are targeted to the appropriate gene promoters in vertebrates and how they influence gene expression have remained poorly defined. Here, using a combination of live-cell imaging and functional genomics, we discover that the vertebrate SET1 complex is targeted to actively transcribed gene promoters through CFP1, which engages in a form of multivalent chromatin reading that involves recognition of non-methylated DNA and histone H3 lysine 4 trimethylation (H3K4me3). CFP1 defines SET1 complex occupancy on chromatin, and its multivalent interactions are required for the SET1 complex to place H3K4me3. In the absence of CFP1, gene expression is perturbed, suggesting that normal targeting and function of the SET1 complex are central to creating an appropriately functioning vertebrate promoter-associated epigenome. Cell Press 2017-09-05 /pmc/articles/PMC5603731/ /pubmed/28877467 http://dx.doi.org/10.1016/j.celrep.2017.08.030 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Brown, David A. Di Cerbo, Vincenzo Feldmann, Angelika Ahn, Jaewoo Ito, Shinsuke Blackledge, Neil P. Nakayama, Manabu McClellan, Michael Dimitrova, Emilia Turberfield, Anne H. Long, Hannah K. King, Hamish W. Kriaucionis, Skirmantas Schermelleh, Lothar Kutateladze, Tatiana G. Koseki, Haruhiko Klose, Robert J. The SET1 Complex Selects Actively Transcribed Target Genes via Multivalent Interaction with CpG Island Chromatin |
title | The SET1 Complex Selects Actively Transcribed Target Genes via Multivalent Interaction with CpG Island Chromatin |
title_full | The SET1 Complex Selects Actively Transcribed Target Genes via Multivalent Interaction with CpG Island Chromatin |
title_fullStr | The SET1 Complex Selects Actively Transcribed Target Genes via Multivalent Interaction with CpG Island Chromatin |
title_full_unstemmed | The SET1 Complex Selects Actively Transcribed Target Genes via Multivalent Interaction with CpG Island Chromatin |
title_short | The SET1 Complex Selects Actively Transcribed Target Genes via Multivalent Interaction with CpG Island Chromatin |
title_sort | set1 complex selects actively transcribed target genes via multivalent interaction with cpg island chromatin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603731/ https://www.ncbi.nlm.nih.gov/pubmed/28877467 http://dx.doi.org/10.1016/j.celrep.2017.08.030 |
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