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A non-canonical monovalent zinc finger stabilizes the integration of Cfp1 into the H3K4 methyltransferase complex COMPASS
COMPlex ASsociating with SET1 (COMPASS) is a histone H3 Lys-4 methyltransferase that typically marks the promoter region of actively transcribed genes. COMPASS is a multi-subunit complex in which the catalytic unit, SET1, is required for H3K4 methylation. An important subunit known to regulate SET1...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145517/ https://www.ncbi.nlm.nih.gov/pubmed/31724694 http://dx.doi.org/10.1093/nar/gkz1037 |
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author | Yang, Yidai Joshi, Monika Takahashi, Yoh-hei Ning, Zhibin Qu, Qianhui Brunzelle, Joseph S Skiniotis, Georgios Figeys, Daniel Shilatifard, Ali Couture, Jean-François |
author_facet | Yang, Yidai Joshi, Monika Takahashi, Yoh-hei Ning, Zhibin Qu, Qianhui Brunzelle, Joseph S Skiniotis, Georgios Figeys, Daniel Shilatifard, Ali Couture, Jean-François |
author_sort | Yang, Yidai |
collection | PubMed |
description | COMPlex ASsociating with SET1 (COMPASS) is a histone H3 Lys-4 methyltransferase that typically marks the promoter region of actively transcribed genes. COMPASS is a multi-subunit complex in which the catalytic unit, SET1, is required for H3K4 methylation. An important subunit known to regulate SET1 methyltransferase activity is the CxxC zinc finger protein 1 (Cfp1). Cfp1 binds to COMPASS and is critical to maintain high level of H3K4me3 in cells but the mechanisms underlying its stimulatory activity is poorly understood. In this study, we show that Cfp1 only modestly activates COMPASS methyltransferase activity in vitro. Binding of Cfp1 to COMPASS is in part mediated by a new type of monovalent zinc finger (ZnF). This ZnF interacts with the COMPASS’s subunits RbBP5 and disruption of this interaction blunts its methyltransferase activity in cells and in vivo. Collectively, our studies reveal that a novel form of ZnF on Cfp1 enables its integration into COMPASS and contributes to epigenetic signaling. |
format | Online Article Text |
id | pubmed-7145517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71455172020-04-13 A non-canonical monovalent zinc finger stabilizes the integration of Cfp1 into the H3K4 methyltransferase complex COMPASS Yang, Yidai Joshi, Monika Takahashi, Yoh-hei Ning, Zhibin Qu, Qianhui Brunzelle, Joseph S Skiniotis, Georgios Figeys, Daniel Shilatifard, Ali Couture, Jean-François Nucleic Acids Res Structural Biology COMPlex ASsociating with SET1 (COMPASS) is a histone H3 Lys-4 methyltransferase that typically marks the promoter region of actively transcribed genes. COMPASS is a multi-subunit complex in which the catalytic unit, SET1, is required for H3K4 methylation. An important subunit known to regulate SET1 methyltransferase activity is the CxxC zinc finger protein 1 (Cfp1). Cfp1 binds to COMPASS and is critical to maintain high level of H3K4me3 in cells but the mechanisms underlying its stimulatory activity is poorly understood. In this study, we show that Cfp1 only modestly activates COMPASS methyltransferase activity in vitro. Binding of Cfp1 to COMPASS is in part mediated by a new type of monovalent zinc finger (ZnF). This ZnF interacts with the COMPASS’s subunits RbBP5 and disruption of this interaction blunts its methyltransferase activity in cells and in vivo. Collectively, our studies reveal that a novel form of ZnF on Cfp1 enables its integration into COMPASS and contributes to epigenetic signaling. Oxford University Press 2020-01-10 2019-11-14 /pmc/articles/PMC7145517/ /pubmed/31724694 http://dx.doi.org/10.1093/nar/gkz1037 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Structural Biology Yang, Yidai Joshi, Monika Takahashi, Yoh-hei Ning, Zhibin Qu, Qianhui Brunzelle, Joseph S Skiniotis, Georgios Figeys, Daniel Shilatifard, Ali Couture, Jean-François A non-canonical monovalent zinc finger stabilizes the integration of Cfp1 into the H3K4 methyltransferase complex COMPASS |
title | A non-canonical monovalent zinc finger stabilizes the integration of Cfp1 into the H3K4 methyltransferase complex COMPASS |
title_full | A non-canonical monovalent zinc finger stabilizes the integration of Cfp1 into the H3K4 methyltransferase complex COMPASS |
title_fullStr | A non-canonical monovalent zinc finger stabilizes the integration of Cfp1 into the H3K4 methyltransferase complex COMPASS |
title_full_unstemmed | A non-canonical monovalent zinc finger stabilizes the integration of Cfp1 into the H3K4 methyltransferase complex COMPASS |
title_short | A non-canonical monovalent zinc finger stabilizes the integration of Cfp1 into the H3K4 methyltransferase complex COMPASS |
title_sort | non-canonical monovalent zinc finger stabilizes the integration of cfp1 into the h3k4 methyltransferase complex compass |
topic | Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145517/ https://www.ncbi.nlm.nih.gov/pubmed/31724694 http://dx.doi.org/10.1093/nar/gkz1037 |
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