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

Cell Cycle. 2014;13(5):726-38. doi: 10.4161/cc.28104. Epub 2014 Feb 6.

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 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.

Keywords: DOT1L; H3K79; cell cycle; differentiation; histone methyltransferase; meiosis; mitosis; proliferation; replication; senescence.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cell Cycle*
  • Cellular Reprogramming
  • Chromatin / genetics
  • Chromatin / metabolism*
  • DNA Damage
  • Histone-Lysine N-Methyltransferase
  • Histones / metabolism
  • Humans
  • Lysine / metabolism
  • Methylation
  • Methyltransferases / metabolism*
  • Neoplasms / metabolism
  • Neoplasms / pathology

Substances

  • Chromatin
  • Histones
  • DOT1L protein, human
  • Methyltransferases
  • Histone-Lysine N-Methyltransferase
  • Lysine