The Drosophila NURF remodelling and the ATAC histone acetylase complexes functionally interact and are required for global chromosome organization

EMBO Rep. 2008 Feb;9(2):187-92. doi: 10.1038/sj.embor.7401141. Epub 2007 Dec 14.

Abstract

Drosophila Gcn5 is the catalytic subunit of the SAGA and ATAC histone acetylase complexes. Here, we show that mutations in Gcn5 and the ATAC component Ada2a induce a decondensation of the male X chromosome, similar to that induced by mutations in the Iswi and Nurf301 subunits of the NURF nucleosome remodelling complex. Genetic studies as well as transcript profiling analysis indicate that ATAC and NURF regulate overlapping sets of target genes during development. In addition, we find that Ada2a chromosome binding and histone H4-Lys12 acetylation are compromised in Iswi and Nurf301 mutants. Our results strongly suggest that NURF is required for ATAC to access the chromatin and to regulate global chromosome organization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Adenosine Triphosphatases / metabolism
  • Animals
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster / cytology
  • Drosophila melanogaster / enzymology*
  • Drosophila melanogaster / genetics
  • Genes, Insect
  • Histone Acetyltransferases / metabolism*
  • Larva
  • Male
  • Multiprotein Complexes / metabolism*
  • Mutation / genetics
  • Protein Binding
  • Protein Subunits / metabolism
  • Transcription Factors / metabolism
  • X Chromosome / metabolism*

Substances

  • Drosophila Proteins
  • ISWI protein
  • Multiprotein Complexes
  • Protein Subunits
  • Transcription Factors
  • GCN5 protein, Drosophila
  • Histone Acetyltransferases
  • Adenosine Triphosphatases