The Protein Sex-lethal Antagonizes the Splicing Factor U2AF to Regulate Alternative Splicing of Transformer pre-mRNA

Nature. 1993 Mar 11;362(6416):171-5. doi: 10.1038/362171a0.

Abstract

Somatic sexual differentiation in Drosophila melanogaster involves a cascade of regulated splicing events and provides an attractive model system for the analysis of alternative splicing mechanisms. The protein Sex-lethal (Sxl) activates a female-specific 3' splice site in the first intron of transformer (tra) pre-mRNA while repressing an alternative non-sex-specific site. We have developed an in vitro system that recapitulates this regulation in a manner consistent with genetic, transfection and fly transformation studies. Using this system, we have determined the molecular basis of the splice site switch. Here we show that Sxl inhibits splicing to the non-sex-specific (default) site by specifically binding to its polypyrimidine tract, blocking the binding of the essential splicing factor U2AF. This enables U2AF to activate the lower-affinity female-specific site. A splicing 'effector' domain present in U2AF but absent from Sxl accounts for the different activities of these two polypyrimidine-tract-binding proteins: addition of the U2AF effector domain to Sxl converts it from a splicing repressor to an activator and renders it unable to mediate splice-site switching.

Publication types

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

MeSH terms

  • Alternative Splicing*
  • Animals
  • Animals, Genetically Modified
  • Base Sequence
  • Drosophila Proteins*
  • Drosophila melanogaster / genetics*
  • Drosophila melanogaster / physiology
  • Female
  • Genes, Lethal
  • Globins / genetics
  • Humans
  • Insect Hormones / metabolism*
  • Introns
  • Male
  • Molecular Sequence Data
  • Nuclear Proteins*
  • Polymerase Chain Reaction / methods
  • RNA / genetics
  • RNA / isolation & purification
  • RNA Precursors / genetics
  • RNA Precursors / metabolism*
  • RNA Splicing
  • RNA-Binding Proteins*
  • Recombinant Proteins / metabolism
  • Ribonucleoproteins / metabolism*
  • Sex Ratio
  • Splicing Factor U2AF

Substances

  • Drosophila Proteins
  • Insect Hormones
  • Nuclear Proteins
  • RNA Precursors
  • RNA-Binding Proteins
  • Recombinant Proteins
  • Ribonucleoproteins
  • Splicing Factor U2AF
  • Sxl protein, Drosophila
  • U2AF2 protein, human
  • RNA
  • Globins