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

Research output: Contribution to journal › Review article › peer-review

107 Citations (Scopus)

Abstract

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 G1 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.

Original languageEnglish
Pages (from-to)726-738
Number of pages13
JournalCell Cycle
Volume13
Issue number5
DOIs
Publication statusPublished - 1 Mar 2014

Bibliographical note

Funding Information:
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIP) (No. 2012R1A2A2A01011164 and No.2011-0030072).

Keywords

  • Cell cycle
  • DOT1L
  • Differentiation
  • H3K79
  • Histone methyltransferase
  • Meiosis
  • Mitosis
  • Proliferation
  • Replication
  • Senescence

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