X-chromosome hyperactivation in mammals via nonlinear relationships between chromatin states and transcription

Nat Struct Mol Biol. 2011 Dec 4;19(1):56-61. doi: 10.1038/nsmb.2195.

Abstract

Dosage compensation in mammals occurs at two levels. In addition to balancing X-chromosome dosage between males and females via X inactivation, mammals also balance dosage of Xs and autosomes. It has been proposed that X-autosome equalization occurs by upregulation of Xa (active X). To investigate mechanism, we perform allele-specific ChIP-seq for chromatin epitopes and analyze RNA-seq data. The hypertranscribed Xa demonstrates enrichment of active chromatin marks relative to autosomes. We derive predictive models for relationships among Pol II occupancy, active mark densities and gene expression, and we suggest that Xa upregulation involves increased transcription initiation and elongation. Enrichment of active marks on Xa does not scale proportionally with transcription output, a disparity explained by nonlinear quantitative dependencies among active histone marks, Pol II occupancy and transcription. Notably, the trend of nonlinear upregulation also occurs on autosomes. Thus, Xa upregulation involves combined increases of active histone marks and Pol II occupancy, without invoking X-specific dependencies between chromatin states and transcription.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Chromatin / genetics*
  • Chromatin / metabolism
  • Chromosomes, Mammalian / genetics
  • DNA Polymerase II / metabolism
  • Dosage Compensation, Genetic*
  • Female
  • Gene Expression Profiling
  • Genes, X-Linked / genetics
  • Histones / metabolism
  • Lysine / metabolism
  • Male
  • Methylation
  • Mice
  • Mice, 129 Strain
  • Models, Genetic
  • Oligonucleotide Array Sequence Analysis
  • Promoter Regions, Genetic / genetics
  • Transcription Initiation Site
  • Transcription, Genetic*
  • X Chromosome / genetics*

Substances

  • Chromatin
  • Histones
  • DNA Polymerase II
  • Lysine

Associated data

  • GEO/GSE33823