Rpp29 regulates histone H3.3 chromatin assembly through transcriptional mechanisms

J Biol Chem. 2018 Aug 10;293(32):12360-12377. doi: 10.1074/jbc.RA118.001845. Epub 2018 Jun 19.

Abstract

The histone H3 variant H3.3 is a highly conserved and dynamic regulator of chromatin organization. Therefore, fully elucidating its nucleosome incorporation mechanisms is essential to understanding its functions in epigenetic inheritance. We previously identified the RNase P protein subunit, Rpp29, as a repressor of H3.3 chromatin assembly. Here, we use a biochemical assay to show that Rpp29 interacts with H3.3 through a sequence element in its own N terminus, and we identify a novel interaction with histone H2B at an adjacent site. The fact that archaeal Rpp29 does not include this N-terminal region suggests that it evolved to regulate eukaryote-specific functions. Oncogenic H3.3 mutations alter the H3.3-Rpp29 interaction, which suggests that they could dysregulate Rpp29 function in chromatin assembly. We also used KNS42 cells, an H3.3(G34V) pediatric high-grade glioma cell line, to show that Rpp29 1) represses H3.3 incorporation into transcriptionally active protein-coding, rRNA, and tRNA genes; 2) represses mRNA, protein expression, and antisense RNA; and 3) represses euchromatic post-translational modifications (PTMs) and promotes heterochromatic PTM deposition (i.e. histone H3 Lys-9 trimethylation (H3K9me3) and H3.1/2/3K27me3). Notably, we also found that K27me2 is increased and K36me1 decreased on H3.3(G34V), which suggests that Gly-34 mutations dysregulate Lys-27 and Lys-36 methylation in cis The fact that Rpp29 represses H3.3 chromatin assembly and sense and antisense RNA and promotes H3K9me3 and H3K27me3 suggests that Rpp29 regulates H3.3-mediated epigenetic mechanisms by processing a transcribed signal that recruits H3.3 to its incorporation sites.

Keywords: RNase P; Rpp29; antisense RNA; chromatin regulation; epigenetics; gene regulation; glioblastoma; histone H3.3; histone modification; histone post-translational modifications (PTMs); transcription.

Publication types

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

MeSH terms

  • Chromatin Assembly and Disassembly*
  • Epigenesis, Genetic*
  • Glioma / genetics
  • Glioma / metabolism*
  • Glioma / pathology
  • Histones / genetics
  • Histones / metabolism*
  • Humans
  • Methylation
  • Mutation
  • Nucleosomes / genetics
  • Nucleosomes / metabolism*
  • Ribonucleases / genetics
  • Ribonucleases / metabolism*
  • Ribonucleoproteins / genetics
  • Ribonucleoproteins / metabolism*
  • Transcription, Genetic*
  • Tumor Cells, Cultured

Substances

  • Histones
  • Nucleosomes
  • Ribonucleoproteins
  • Ribonucleases
  • POP4 protein, human