Histones Are Rapidly Loaded onto Unintegrated Retroviral DNAs Soon after Nuclear Entry

Cell Host Microbe. 2016 Dec 14;20(6):798-809. doi: 10.1016/j.chom.2016.10.009. Epub 2016 Nov 17.

Abstract

Chromosomal structure of nuclear DNA is usually maintained by insertion of nucleosomes into preexisting chromatin, both on newly synthesized DNA at replication forks and at sites of DNA damage. But during retrovirus infection, a histone-free DNA copy of the viral genome is synthesized that must be loaded with nucleosomes de novo. Here, we show that core histones are rapidly loaded onto unintegrated Moloney murine leukemia virus DNAs. Loading of nucleosomes requires nuclear entry, but does not require viral DNA integration. The histones associated with unintegrated DNAs become marked by covalent modifications, with a delay relative to the time of core histone loading. Expression from unintegrated DNA can be enhanced by modulation of the histone-modifying machinery. The data show that histone loading onto unintegrated DNAs occurs very rapidly after nuclear entry and does not require prior establishment of an integrated provirus.

Keywords: chromatin immunoprecipitation; epigenetics; histone; histone modifications; nucleosome; retrovirus.

MeSH terms

  • Animals
  • Cell Cycle
  • Chromatin
  • Chromatin Immunoprecipitation
  • DNA Damage
  • DNA Replication / genetics
  • DNA, Viral* / analysis
  • Epigenomics
  • HEK293 Cells / virology
  • Histone Code*
  • Histones / metabolism*
  • Humans
  • Mice
  • Moloney murine leukemia virus / genetics
  • NIH 3T3 Cells / virology
  • Nucleosomes / genetics
  • Retroviridae / genetics*
  • Retroviridae Infections / virology
  • Virus Integration
  • Virus Internalization*

Substances

  • Chromatin
  • DNA, Viral
  • Histones
  • Nucleosomes