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DNMTs and SETDB1 function as co-repressors in MAX-mediated repression of germ cell–related genes in mouse embryonic stem cells

In embryonic stem cells (ESCs), the expression of development-related genes, including germ cell–related genes, is globally repressed. The transcription factor MAX represses germ cell–related gene expression in ESCs via PCGF6-polycomb repressive complex 1 (PRC1), which consists of several epigenetic...

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Autores principales: Tatsumi, Daiki, Hayashi, Yohei, Endo, Mai, Kobayashi, Hisato, Yoshioka, Takumi, Kiso, Kohei, Kanno, Shinichiro, Nakai, Yuji, Maeda, Ikuma, Mochizuki, Kentaro, Tachibana, Makoto, Koseki, Haruhiko, Okuda, Akihiko, Yasui, Akira, Kono, Tomohiro, Matsui, Yasuhisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221296/
https://www.ncbi.nlm.nih.gov/pubmed/30403691
http://dx.doi.org/10.1371/journal.pone.0205969
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author Tatsumi, Daiki
Hayashi, Yohei
Endo, Mai
Kobayashi, Hisato
Yoshioka, Takumi
Kiso, Kohei
Kanno, Shinichiro
Nakai, Yuji
Maeda, Ikuma
Mochizuki, Kentaro
Tachibana, Makoto
Koseki, Haruhiko
Okuda, Akihiko
Yasui, Akira
Kono, Tomohiro
Matsui, Yasuhisa
author_facet Tatsumi, Daiki
Hayashi, Yohei
Endo, Mai
Kobayashi, Hisato
Yoshioka, Takumi
Kiso, Kohei
Kanno, Shinichiro
Nakai, Yuji
Maeda, Ikuma
Mochizuki, Kentaro
Tachibana, Makoto
Koseki, Haruhiko
Okuda, Akihiko
Yasui, Akira
Kono, Tomohiro
Matsui, Yasuhisa
author_sort Tatsumi, Daiki
collection PubMed
description In embryonic stem cells (ESCs), the expression of development-related genes, including germ cell–related genes, is globally repressed. The transcription factor MAX represses germ cell–related gene expression in ESCs via PCGF6-polycomb repressive complex 1 (PRC1), which consists of several epigenetic factors. However, we predicted that MAX represses germ cell–related gene expression through several additional mechanisms because PCGF6-PRC1 regulates the expression of only a subset of genes repressed by MAX. Here, we report that MAX associated with DNA methyltransferases (DNMTs) and the histone methyltransferase SETDB1 cooperatively control germ cell–related gene expression in ESCs. Both DNA methylation and histone H3 lysine 9 tri-methylation of the promoter regions of several germ cell–related genes were not affected by knockout of the PRC1 components, indicating that the MAX-DNMT and MAX-SETDB1 pathways are independent of the PCGF6-PRC1 pathway. Our findings provide insights into our understanding of MAX-based repressive mechanisms of germ cell–related genes in ESCs.
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spelling pubmed-62212962018-11-19 DNMTs and SETDB1 function as co-repressors in MAX-mediated repression of germ cell–related genes in mouse embryonic stem cells Tatsumi, Daiki Hayashi, Yohei Endo, Mai Kobayashi, Hisato Yoshioka, Takumi Kiso, Kohei Kanno, Shinichiro Nakai, Yuji Maeda, Ikuma Mochizuki, Kentaro Tachibana, Makoto Koseki, Haruhiko Okuda, Akihiko Yasui, Akira Kono, Tomohiro Matsui, Yasuhisa PLoS One Research Article In embryonic stem cells (ESCs), the expression of development-related genes, including germ cell–related genes, is globally repressed. The transcription factor MAX represses germ cell–related gene expression in ESCs via PCGF6-polycomb repressive complex 1 (PRC1), which consists of several epigenetic factors. However, we predicted that MAX represses germ cell–related gene expression through several additional mechanisms because PCGF6-PRC1 regulates the expression of only a subset of genes repressed by MAX. Here, we report that MAX associated with DNA methyltransferases (DNMTs) and the histone methyltransferase SETDB1 cooperatively control germ cell–related gene expression in ESCs. Both DNA methylation and histone H3 lysine 9 tri-methylation of the promoter regions of several germ cell–related genes were not affected by knockout of the PRC1 components, indicating that the MAX-DNMT and MAX-SETDB1 pathways are independent of the PCGF6-PRC1 pathway. Our findings provide insights into our understanding of MAX-based repressive mechanisms of germ cell–related genes in ESCs. Public Library of Science 2018-11-07 /pmc/articles/PMC6221296/ /pubmed/30403691 http://dx.doi.org/10.1371/journal.pone.0205969 Text en © 2018 Tatsumi et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Tatsumi, Daiki
Hayashi, Yohei
Endo, Mai
Kobayashi, Hisato
Yoshioka, Takumi
Kiso, Kohei
Kanno, Shinichiro
Nakai, Yuji
Maeda, Ikuma
Mochizuki, Kentaro
Tachibana, Makoto
Koseki, Haruhiko
Okuda, Akihiko
Yasui, Akira
Kono, Tomohiro
Matsui, Yasuhisa
DNMTs and SETDB1 function as co-repressors in MAX-mediated repression of germ cell–related genes in mouse embryonic stem cells
title DNMTs and SETDB1 function as co-repressors in MAX-mediated repression of germ cell–related genes in mouse embryonic stem cells
title_full DNMTs and SETDB1 function as co-repressors in MAX-mediated repression of germ cell–related genes in mouse embryonic stem cells
title_fullStr DNMTs and SETDB1 function as co-repressors in MAX-mediated repression of germ cell–related genes in mouse embryonic stem cells
title_full_unstemmed DNMTs and SETDB1 function as co-repressors in MAX-mediated repression of germ cell–related genes in mouse embryonic stem cells
title_short DNMTs and SETDB1 function as co-repressors in MAX-mediated repression of germ cell–related genes in mouse embryonic stem cells
title_sort dnmts and setdb1 function as co-repressors in max-mediated repression of germ cell–related genes in mouse embryonic stem cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221296/
https://www.ncbi.nlm.nih.gov/pubmed/30403691
http://dx.doi.org/10.1371/journal.pone.0205969
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