Enhancer of Rudimentary Cooperates with Conserved RNA-Processing Factors to Promote Meiotic mRNA Decay and Facultative Heterochromatin Assembly

Mol Cell. 2016 Mar 3;61(5):747-759. doi: 10.1016/j.molcel.2016.01.029.

Abstract

Erh1, the fission yeast homolog of Enhancer of rudimentary, is implicated in meiotic mRNA elimination during vegetative growth, but its function is poorly understood. We show that Erh1 and the RNA-binding protein Mmi1 form a stoichiometric complex, called the Erh1-Mmi1 complex (EMC), to promote meiotic mRNA decay and facultative heterochromatin assembly. To perform these functions, EMC associates with two distinct complexes, Mtl1-Red1 core (MTREC) and CCR4-NOT. Whereas MTREC facilitates assembly of heterochromatin islands coating meiotic genes silenced by the nuclear exosome, CCR4-NOT promotes RNAi-dependent heterochromatin domain (HOOD) formation at EMC-target loci. CCR4-NOT also assembles HOODs at retrotransposons and regulated genes containing cryptic introns. We find that CCR4-NOT facilitates HOOD assembly through its association with the conserved Pir2/ARS2 protein, and also maintains rDNA integrity and silencing by promoting heterochromatin formation. Our results reveal connections among Erh1, CCR4-NOT, Pir2/ARS2, and RNAi, which target heterochromatin to regulate gene expression and protect genome integrity.

Publication types

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

MeSH terms

  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Chromatin Assembly and Disassembly*
  • DNA, Ribosomal / genetics
  • DNA, Ribosomal / metabolism
  • Gene Expression Regulation, Fungal
  • Heterochromatin / genetics
  • Heterochromatin / metabolism*
  • Meiosis*
  • Mutation
  • Nucleic Acid Conformation
  • Protein Binding
  • RNA Interference*
  • RNA Stability*
  • RNA, Fungal / genetics
  • RNA, Fungal / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism
  • Retroelements
  • Schizosaccharomyces / genetics
  • Schizosaccharomyces / growth & development
  • Schizosaccharomyces / metabolism*
  • Schizosaccharomyces pombe Proteins / genetics
  • Schizosaccharomyces pombe Proteins / metabolism*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • mRNA Cleavage and Polyadenylation Factors / genetics
  • mRNA Cleavage and Polyadenylation Factors / metabolism*

Substances

  • Carrier Proteins
  • DNA, Ribosomal
  • Erh1 protein, S pombe
  • Heterochromatin
  • Mmi1 protein, S pombe
  • RNA, Fungal
  • RNA, Messenger
  • RNA-Binding Proteins
  • Red1 protein, S pombe
  • Retroelements
  • Schizosaccharomyces pombe Proteins
  • Transcription Factors
  • mRNA Cleavage and Polyadenylation Factors
  • mei2 protein, S pombe