Hap2–Ino80-facilitated transcription promotes de novo establishment of CENP-A chromatin

Puneet P. Singh, Manu Shukla, Sharon A. White, Marcel Lafos, Pin Tong, Tatsiana Auchynnikava, Christos Spanos, Juri Rappsilber, Alison L. Pidoux, Robin C. Allshire

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

Centromeres are maintained epigenetically by the presence of CENP-A, an evolutionarily conserved histone H3 variant, which directs kinetochore assembly and hence centromere function. To identify factors that promote assembly of CENP-A chromatin, we affinity-selected solubilized fission yeast CENP-ACnp1 chromatin. All subunits of the Ino80 complex were enriched, including the auxiliary subunit Hap2. Chromatin association of Hap2 is Ies4-dependent. In addition to a role in maintenance of CENP-ACnp1 chromatin integrity at endogenous centromeres, Hap2 is required for de novo assembly of CENP-ACnp1 chromatin on naïve centromere DNA and promotes H3 turnover on centromere regions and other loci prone to CENP-ACnp1 deposition. Prior to CENP-ACnp1 chromatin assembly, Hap2 facilitates transcription from centromere DNA. These analyses suggest that Hap2–Ino80 destabilizes H3 nucleosomes on centromere DNA through transcription-coupled histone H3 turnover, driving the replacement of resident H3 nucleosomes with CENP-ACnp1 nucleosomes. These inherent properties define centromere DNA by directing a program that mediates CENP-ACnp1 assembly on appropriate sequences.
Original languageEnglish
Pages (from-to)226-238
JournalGenes & Development
Issue number3-4
Early online date9 Jan 2020
Publication statusE-pub ahead of print - 9 Jan 2020

Keywords / Materials (for Non-textual outputs)

  • CENP-A
  • centromere
  • chromatin
  • chromosome segregation
  • epigenetic
  • fission yeast
  • histone
  • kintectochore
  • remodeling
  • transcription


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