Distinct binding specificities and functions of higher eukaryotic polypyrimidine tract-binding proteins

Science. 1995 May 26;268(5214):1173-6. doi: 10.1126/science.7761834.

Abstract

In higher eukaryotes, the polypyrimidine-tract (Py-tract) adjacent to the 3' splice site is recognized by several proteins, including the essential splicing factor U2AF65, the splicing regulator Sex-lethal (Sxl), and polypyrimidine tract-binding protein (PTB), whose function is unknown. Iterative in vitro genetic selection was used to show that these proteins have distinct sequence preferences. The uridine-rich degenerate sequences selected by U2AF65 are similar to those present in the diverse array of natural metazoan Py-tracts. In contrast, the Sxl-consensus is a highly specific sequence, which can help explain the ability of Sxl to regulate splicing of transformer pre-mRNA and autoregulate splicing of its own pre-mRNA. The PTB-consensus is not a typical Py-tract; it can be found in certain alternatively spliced pre-mRNAs that undergo negative regulation. Here it is shown that PTB can regulate alternative splicing by selectively repressing 3' splice sites that contain a PTB-binding site.

Publication types

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

MeSH terms

  • Animals
  • Base Sequence
  • Binding Sites
  • Consensus Sequence
  • DNA, Complementary
  • Drosophila
  • Drosophila Proteins*
  • Female
  • Humans
  • Insect Hormones / metabolism
  • Male
  • Molecular Sequence Data
  • Nuclear Proteins*
  • Polypyrimidine Tract-Binding Protein
  • RNA Splicing*
  • RNA-Binding Proteins / metabolism*
  • Ribonucleoproteins / metabolism*
  • Splicing Factor U2AF

Substances

  • DNA, Complementary
  • Drosophila Proteins
  • Insect Hormones
  • Nuclear Proteins
  • RNA-Binding Proteins
  • Ribonucleoproteins
  • Splicing Factor U2AF
  • Sxl protein, Drosophila
  • U2AF2 protein, human
  • Polypyrimidine Tract-Binding Protein