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SETDB1-Mediated Silencing of Retroelements

SETDB1 (SET domain bifurcated histone lysine methyltransferase 1) is a protein lysine methyltransferase and methylates histone H3 at lysine 9 (H3K9). Among other H3K9 methyltransferases, SETDB1 and SETDB1-mediated H3K9 trimethylation (H3K9me3) play pivotal roles for silencing of endogenous and exoge...

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Autores principales: Fukuda, Kei, Shinkai, Yoichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354471/
https://www.ncbi.nlm.nih.gov/pubmed/32486217
http://dx.doi.org/10.3390/v12060596
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author Fukuda, Kei
Shinkai, Yoichi
author_facet Fukuda, Kei
Shinkai, Yoichi
author_sort Fukuda, Kei
collection PubMed
description SETDB1 (SET domain bifurcated histone lysine methyltransferase 1) is a protein lysine methyltransferase and methylates histone H3 at lysine 9 (H3K9). Among other H3K9 methyltransferases, SETDB1 and SETDB1-mediated H3K9 trimethylation (H3K9me3) play pivotal roles for silencing of endogenous and exogenous retroelements, thus contributing to genome stability against retroelement transposition. Furthermore, SETDB1 is highly upregulated in various tumor cells. In this article, we describe recent advances about how SETDB1 activity is regulated, how SETDB1 represses various types of retroelements such as L1 and class I, II, and III endogenous retroviruses (ERVs) in concert with other epigenetic factors such as KAP1 and the HUSH complex and how SETDB1-mediated H3K9 methylation can be maintained during replication.
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spelling pubmed-73544712020-08-05 SETDB1-Mediated Silencing of Retroelements Fukuda, Kei Shinkai, Yoichi Viruses Review SETDB1 (SET domain bifurcated histone lysine methyltransferase 1) is a protein lysine methyltransferase and methylates histone H3 at lysine 9 (H3K9). Among other H3K9 methyltransferases, SETDB1 and SETDB1-mediated H3K9 trimethylation (H3K9me3) play pivotal roles for silencing of endogenous and exogenous retroelements, thus contributing to genome stability against retroelement transposition. Furthermore, SETDB1 is highly upregulated in various tumor cells. In this article, we describe recent advances about how SETDB1 activity is regulated, how SETDB1 represses various types of retroelements such as L1 and class I, II, and III endogenous retroviruses (ERVs) in concert with other epigenetic factors such as KAP1 and the HUSH complex and how SETDB1-mediated H3K9 methylation can be maintained during replication. MDPI 2020-05-30 /pmc/articles/PMC7354471/ /pubmed/32486217 http://dx.doi.org/10.3390/v12060596 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Fukuda, Kei
Shinkai, Yoichi
SETDB1-Mediated Silencing of Retroelements
title SETDB1-Mediated Silencing of Retroelements
title_full SETDB1-Mediated Silencing of Retroelements
title_fullStr SETDB1-Mediated Silencing of Retroelements
title_full_unstemmed SETDB1-Mediated Silencing of Retroelements
title_short SETDB1-Mediated Silencing of Retroelements
title_sort setdb1-mediated silencing of retroelements
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354471/
https://www.ncbi.nlm.nih.gov/pubmed/32486217
http://dx.doi.org/10.3390/v12060596
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