C. elegans Heterochromatin Factor SET-32 Plays an Essential Role in Transgenerational Establishment of Nuclear RNAi-Mediated Epigenetic Silencing

Cell Rep. 2018 Nov 20;25(8):2273-2284.e3. doi: 10.1016/j.celrep.2018.10.086.

Abstract

The dynamic process by which nuclear RNAi engages a transcriptionally active target, before the repressive state is stably established, remains largely a mystery. Here, we found that the onset of exogenous dsRNA-induced nuclear RNAi in C. elegans is a transgenerational process, and it requires a putative histone methyltransferase (HMT), SET-32. By developing a CRISPR-based genetic approach, we found that silencing establishment at the endogenous targets of germline nuclear RNAi also requires SET-32. Although SET-32 and two H3K9 HMTs, MET-2 and SET-25, are dispensable for the maintenance of silencing, they do contribute to transcriptional repression in mutants that lack the germline nuclear Argonaute protein HRDE-1, suggesting a conditional role of heterochromatin in the maintenance phase. Our study indicates that (1) establishment and maintenance of siRNA-guided transcriptional repression are two distinct processes with different genetic requirements and (2) the rate-limiting step of the establishment phase is a transgenerational, chromatin-based process.

Keywords: CRISPR; HRDE-1; MET-2; SET-25; SET-32; epigenetic silencing; heterochromatin; nuclear RNAi; silencing establishment; transgenerational epigenetic inheritance.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • CRISPR-Cas Systems / genetics
  • Caenorhabditis elegans / genetics*
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / physiology*
  • Epigenesis, Genetic*
  • Germ Cells / metabolism
  • Heterochromatin / metabolism*
  • Histone Methyltransferases / genetics
  • Histone Methyltransferases / physiology*
  • Histones / metabolism
  • Lysine / metabolism
  • Mutation / genetics
  • RNA Interference*
  • RNA, Double-Stranded / metabolism
  • Transcription, Genetic

Substances

  • Caenorhabditis elegans Proteins
  • Heterochromatin
  • Histones
  • RNA, Double-Stranded
  • Histone Methyltransferases
  • set-32 protein, C elegans
  • Lysine