Evolutionary divergence of intrinsic and trans-regulated nucleosome positioning sequences reveals plastic rules for chromatin organization

Genome Res. 2011 Nov;21(11):1851-62. doi: 10.1101/gr.122267.111. Epub 2011 Sep 13.

Abstract

The packaging of eukaryotic genomes into nuclesomes plays critical roles in chromatin organization and gene regulation. Studies in Saccharomyces cerevisiae indicate that nucleosome occupancy is partially encoded by intrinsic antinucleosomal DNA sequences, such as poly(A) sequences, as well as by binding sites for trans-acting factors that can evict nucleosomes, such as Reb1 and the Rsc3/30 complex. Here, we use genome-wide nucleosome occupancy maps in 13 Ascomycota fungi to discover large-scale evolutionary reprogramming of both intrinsic and trans determinants of chromatin structure. We find that poly(G)s act as intrinsic antinucleosomal sequences, comparable to the known function of poly(A)s, but that the abundance of poly(G)s has diverged greatly between species, obscuring their antinucleosomal effect in low-poly(G) species such as S. cerevisiae. We also develop a computational method that uses nucleosome occupancy maps for discovering trans-acting general regulatory factor (GRF) binding sites. Our approach reveals that the specific sequences bound by GRFs have diverged substantially across evolution, corresponding to a number of major evolutionary transitions in the repertoire of GRFs. We experimentally validate a proposed evolutionary transition from Cbf1 as a major GRF in pre-whole-genome duplication (WGD) yeasts to Reb1 in post-WGD yeasts. We further show that the mating type switch-activating protein Sap1 is a GRF in S. pombe, demonstrating the general applicability of our approach. Our results reveal that the underlying mechanisms that determine in vivo chromatin organization have diverged and that comparative genomics can help discover new determinants of chromatin organization.

Publication types

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

MeSH terms

  • Ascomycota / genetics
  • Ascomycota / metabolism
  • Base Sequence
  • Binding Sites / genetics
  • Chromatin / metabolism*
  • Cluster Analysis
  • DNA-Binding Proteins / metabolism
  • Evolution, Molecular*
  • Fungal Proteins / metabolism
  • Gene Expression Regulation, Fungal
  • Genome, Fungal*
  • Nucleosomes / metabolism*
  • Nucleotide Motifs
  • Phylogeny
  • Schizosaccharomyces pombe Proteins / metabolism
  • Sequence Alignment

Substances

  • CBF1 protein, Candida albicans
  • Chromatin
  • DNA-Binding Proteins
  • Fungal Proteins
  • Nucleosomes
  • Sap1 protein, S pombe
  • Schizosaccharomyces pombe Proteins

Associated data

  • GEO/GSE21960
  • GEO/GSE28839