Cutoff Suppresses RNA Polymerase II Termination to Ensure Expression of piRNA Precursors

Mol Cell. 2016 Jul 7;63(1):97-109. doi: 10.1016/j.molcel.2016.05.010. Epub 2016 Jun 9.

Abstract

Small non-coding RNAs called piRNAs serve as guides for an adaptable immune system that represses transposable elements in germ cells of Metazoa. In Drosophila the RDC complex, composed of Rhino, Deadlock and Cutoff (Cuff) bind chromatin of dual-strand piRNA clusters, special genomic regions, which encode piRNA precursors. The RDC complex is required for transcription of piRNA precursors, though the mechanism by which it licenses transcription remained unknown. Here, we show that Cuff prevents premature termination of RNA polymerase II. Cuff prevents cleavage of nascent RNA at poly(A) sites by interfering with recruitment of the cleavage and polyadenylation specificity factor (CPSF) complex. Cuff also protects processed transcripts from degradation by the exonuclease Rat1. Our work reveals a conceptually different mechanism of transcriptional enhancement. In contrast to other factors that regulate termination by binding to specific signals on nascent RNA, the RDC complex inhibits termination in a chromatin-dependent and sequence-independent manner.

MeSH terms

  • Adenosine / metabolism
  • Animals
  • Animals, Genetically Modified
  • Binding Sites
  • Chromatin / metabolism
  • Chromosomal Proteins, Non-Histone / metabolism
  • Cleavage And Polyadenylation Specificity Factor / metabolism
  • Computational Biology
  • Databases, Genetic
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster / enzymology*
  • Drosophila melanogaster / genetics
  • Exoribonucleases / metabolism
  • Genes, Reporter
  • Microtubule-Associated Proteins / metabolism
  • Multiprotein Complexes
  • Polymers / metabolism
  • Protein Binding
  • RNA Polymerase II / metabolism*
  • RNA Stability
  • RNA, Small Interfering / biosynthesis*
  • RNA, Small Interfering / genetics
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism*
  • Transcription Termination, Genetic
  • Transcription, Genetic*

Substances

  • Chromatin
  • Chromosomal Proteins, Non-Histone
  • Cleavage And Polyadenylation Specificity Factor
  • Cuff protein, Drosophila
  • Drosophila Proteins
  • Microtubule-Associated Proteins
  • Multiprotein Complexes
  • Polymers
  • RNA, Small Interfering
  • RNA-Binding Proteins
  • del protein, Drosophila
  • rhi protein, Drosophila
  • polyadenosine
  • RNA Polymerase II
  • Exoribonucleases
  • Adenosine