The yeast 5'-3' exonuclease Rat1p functions during transcription elongation by RNA polymerase II

Mol Cell. 2010 Feb 26;37(4):580-7. doi: 10.1016/j.molcel.2010.01.019.

Abstract

Termination of RNA polymerase II (RNAPII) transcription of protein-coding genes occurs downstream of cleavage/polyadenylation sites. According to the "torpedo" model, the 5'-3' exonuclease Rat1p/Xrn2p attacks the newly formed 5' end of the cleaved pre-mRNA, causing the still transcribing RNAPII to terminate. Here we demonstrate a similar role of S. cerevisiae Rat1p within the gene body. We find that the transcription processivity defect imposed on RNAPII by the rpb1-N488D mutation is corrected upon Rat1p inactivation. Importantly, Rat1p-dependent transcription termination occurs upstream the polyadenylation site. Genetic and biochemical evidence demonstrate that mRNA capping is defective in rpb1-N488D cells, which leads to increased levels of Rat1p all along the gene locus. Consistently, Rat1p-dependent RNAPII termination is also observed in the capping-deficient ceg1-63 strain. Our data suggest that Rat1p serves to terminate RNAPII molecules engaged in the production of uncapped RNA, regardless of their position on the gene locus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Exoribonucleases / genetics
  • Exoribonucleases / metabolism*
  • Gene Expression Regulation, Fungal
  • Nucleotidyltransferases / genetics
  • Nucleotidyltransferases / metabolism
  • RNA Caps / biosynthesis*
  • RNA Caps / genetics
  • RNA Polymerase II / genetics
  • RNA Polymerase II / metabolism*
  • Saccharomyces cerevisiae / enzymology*
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Transcription, Genetic*
  • mRNA Guanylyltransferases

Substances

  • RNA Caps
  • Saccharomyces cerevisiae Proteins
  • RAT1 protein, S cerevisiae
  • Nucleotidyltransferases
  • RNA Polymerase II
  • RPB1 protein, S cerevisiae
  • mRNA Guanylyltransferases
  • Exoribonucleases