The PRP31 gene encodes a novel protein required for pre-mRNA splicing in Saccharomyces cerevisiae

Nucleic Acids Res. 1996 Mar 15;24(6):1164-70. doi: 10.1093/nar/24.6.1164.

Abstract

The pre-mRNA splicing factor Prp31p was identified in a screen of temperature-sensitive yeast strains for those exhibiting a splicing defect upon shift to the non- permissive temperature. The wild-type PRP31 gene was cloned and shown to be essential for cell viability. The PRP31 gene is predicted to encode a 60 kDa polypeptide. No similarities with other known splicing factors or motifs indicative of protein-protein or RNA-protein interaction domains are discernible in the predicted amino acid sequence. A PRP31 allele bearing a triple repeat of the hemagglutinin epitope has been generated. The tagged protein is functional in vivo and a single polypeptide species of the predicted size was detected by Western analysis with proteins from yeast cell extracts. Functional Prp31p is required for the processing of pre-mRNA species both in vivo and in vitro, indicating that the protein is directly involved in the splicing pathway.

Publication types

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

MeSH terms

  • Cloning, Molecular
  • Fungal Proteins / genetics*
  • Fungal Proteins / metabolism*
  • Genes, Fungal*
  • Mutation
  • RNA Precursors / metabolism*
  • RNA Processing, Post-Transcriptional
  • RNA Splicing / genetics
  • RNA, Fungal / metabolism*
  • Restriction Mapping
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae / metabolism*
  • Temperature

Substances

  • Fungal Proteins
  • RNA Precursors
  • RNA, Fungal