Control of alpha-herpesvirus IE gene expression by HCF-1 coupled chromatin modification activities

Biochim Biophys Acta. 2010 Mar-Apr;1799(3-4):257-65. doi: 10.1016/j.bbagrm.2009.08.003. Epub 2009 Aug 12.

Abstract

The immediate early genes of the alpha-herpesviruses HSV and VZV are transcriptionally regulated by viral and cellular factors in a complex combinatorial manner. Despite this complexity and the apparent redundancy of activators, the expression of the viral IE genes is critically dependent upon the cellular transcriptional coactivator HCF-1. Although the role of HCF-1 had remained elusive, recent studies have demonstrated that the protein is a component of multiple chromatin modification complexes including the Set1/MLL1 histone H3K4 methyltransferases. Studies using model viral promoter-reporter systems as well as analyses of components recruited to the viral genome during the initiation of infection have elucidated the significance of HCF-1 chromatin modification complexes in contributing to the final state of modified histones assembled on the viral IE promoters. Strikingly, the absence of HCF-1 results in the accumulation of nucleosomes bearing repressive marks on the viral IE promoters and silencing of viral gene expression.

Publication types

  • Research Support, N.I.H., Intramural
  • Review

MeSH terms

  • Alphaherpesvirinae / physiology*
  • Chromatin / metabolism*
  • DNA Methylation
  • Gene Expression Regulation, Viral / physiology*
  • Genes, Immediate-Early / genetics*
  • Histones / metabolism
  • Host Cell Factor C1 / genetics
  • Host Cell Factor C1 / metabolism*
  • Humans
  • Transcription, Genetic

Substances

  • Chromatin
  • HCFC1 protein, human
  • Histones
  • Host Cell Factor C1