Dynamic histone modifications mark sex chromosome inactivation and reactivation during mammalian spermatogenesis

Proc Natl Acad Sci U S A. 2004 Nov 23;101(47):16583-7. doi: 10.1073/pnas.0406325101. Epub 2004 Nov 9.

Abstract

Based on the formation of the XY body at pachytene and expression studies of a few X-linked genes, the X and Y chromosomes seem to undergo transcriptional inactivation during mammalian spermatogenesis. However, the extent and the mechanism of X and Y inactivation are not known. Here, we show that both the X and Y chromosomes undergo sequential changes in their histone modifications beginning at the pachytene stage of meiosis. These changes usually are associated with transcriptional inactivation in somatic cells, and they coincide with the exclusion of the phosphorylated (active) form of RNA polymerase II from the XY body. Both sex chromosomes undergo extensive deacetylation at histones H3 and H4 and (di)methylation of lysine (K)9 on histone H3; however, there are no changes in H3-K4 methylation. These changes persist even when the XY body disappears in late pachytene, and the X and Y chromosomes segregate from one another after the first meiotic division. By the spermatid stage, histone modifications of the X and Y chromosomes revert to those of active chromatin and RNA polymerase II reengages with both chromosomes. Our observations indicate that X and Y inactivation is extensive and persists even when the X and Y chromosomes are separated in secondary spermatocytes. These findings provide insights into epigenetic programming and chromatin dynamics in the male germ line.

Publication types

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

MeSH terms

  • Acetylation
  • Animals
  • Dosage Compensation, Genetic*
  • Histones / chemistry
  • Histones / genetics
  • Histones / metabolism*
  • In Situ Hybridization, Fluorescence
  • Male
  • Methylation
  • Mice
  • RNA Polymerase II / metabolism
  • Spermatogenesis / genetics*
  • Spermatogenesis / physiology*
  • X Chromosome / genetics*
  • X Chromosome / metabolism
  • Y Chromosome / genetics*
  • Y Chromosome / metabolism

Substances

  • Histones
  • RNA Polymerase II