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The histone methyltransferase Dot1/DOT1L as a critical regulator of the cell cycle

Dot1/DOT1L catalyzes the methylation of histone H3 lysine 79 (H3K79), which regulates diverse cellular processes, such as development, reprogramming, differentiation, and proliferation. In regards to these processes, studies of Dot1/DOT1L-dependent H3K79 methylation have mainly focused on the transc...

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Detalles Bibliográficos
Autores principales: Kim, Wootae, Choi, Minji, Kim, Ja-Eun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979909/
https://www.ncbi.nlm.nih.gov/pubmed/24526115
http://dx.doi.org/10.4161/cc.28104
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author Kim, Wootae
Choi, Minji
Kim, Ja-Eun
author_facet Kim, Wootae
Choi, Minji
Kim, Ja-Eun
author_sort Kim, Wootae
collection PubMed
description Dot1/DOT1L catalyzes the methylation of histone H3 lysine 79 (H3K79), which regulates diverse cellular processes, such as development, reprogramming, differentiation, and proliferation. In regards to these processes, studies of Dot1/DOT1L-dependent H3K79 methylation have mainly focused on the transcriptional regulation of specific genes. Although the gene transcription mediated by Dot1/DOT1L during the cell cycle is not fully understood, H3K79 methylation plays a critical role in the progression of G(1) phase, S phase, mitosis, and meiosis. This modification may contribute to the chromatin structure that controls gene expression, replication initiation, DNA damage response, microtubule reorganization, chromosome segregation, and heterochromatin formation. Overall, Dot1/DOT1L is required to maintain genomic and chromosomal stability. This review summarizes the several functions of Dot1/DOT1L and highlights its role in cell cycle regulation.
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spelling pubmed-39799092014-04-10 The histone methyltransferase Dot1/DOT1L as a critical regulator of the cell cycle Kim, Wootae Choi, Minji Kim, Ja-Eun Cell Cycle Review Dot1/DOT1L catalyzes the methylation of histone H3 lysine 79 (H3K79), which regulates diverse cellular processes, such as development, reprogramming, differentiation, and proliferation. In regards to these processes, studies of Dot1/DOT1L-dependent H3K79 methylation have mainly focused on the transcriptional regulation of specific genes. Although the gene transcription mediated by Dot1/DOT1L during the cell cycle is not fully understood, H3K79 methylation plays a critical role in the progression of G(1) phase, S phase, mitosis, and meiosis. This modification may contribute to the chromatin structure that controls gene expression, replication initiation, DNA damage response, microtubule reorganization, chromosome segregation, and heterochromatin formation. Overall, Dot1/DOT1L is required to maintain genomic and chromosomal stability. This review summarizes the several functions of Dot1/DOT1L and highlights its role in cell cycle regulation. Landes Bioscience 2014-03-01 2014-02-06 /pmc/articles/PMC3979909/ /pubmed/24526115 http://dx.doi.org/10.4161/cc.28104 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Review
Kim, Wootae
Choi, Minji
Kim, Ja-Eun
The histone methyltransferase Dot1/DOT1L as a critical regulator of the cell cycle
title The histone methyltransferase Dot1/DOT1L as a critical regulator of the cell cycle
title_full The histone methyltransferase Dot1/DOT1L as a critical regulator of the cell cycle
title_fullStr The histone methyltransferase Dot1/DOT1L as a critical regulator of the cell cycle
title_full_unstemmed The histone methyltransferase Dot1/DOT1L as a critical regulator of the cell cycle
title_short The histone methyltransferase Dot1/DOT1L as a critical regulator of the cell cycle
title_sort histone methyltransferase dot1/dot1l as a critical regulator of the cell cycle
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979909/
https://www.ncbi.nlm.nih.gov/pubmed/24526115
http://dx.doi.org/10.4161/cc.28104
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