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Mol. Cell. Biol., Mar 1996, 960-967, Vol 16, No. 3
HY Kao and PG Siliciano
We have used suppressor genetics to identify factors that interact with
Saccharomyces cerevisiae U1 small nuclear RNA (snRNA). In this way, we
isolated PRP40-1, a suppressor that restores growth at 18 degrees C to a
strain bearing a cold-sensitive mutation in U1 RNA. A gene disruption
experiment shows that PRP40 is an essential gene. To study the role of
PRP40 in splicing, we created a pool of temperature-sensitive prp40
strains. Primer extension analysis of intron-containing transcripts in
prp40 temperature-sensitive strains reveals a splicing defect, indicating
that Prp40 plays a direct role in pre-mRNA splicing. In addition, U1 RNA
coimmunoprecipitates with Pro40, indicating that Prp40 is bound to the U1
small nuclear ribonucleoprotein particle in vivo. Therefore, we conclude
that PRP40 encodes a novel, essential splicing component that associates
with the yeast U1 small nuclear ribonucleoprotein particle.
Copyright © 1996, American Society for Microbiology
Identification of Prp40, a novel essential yeast splicing factor associated with the U1 small nuclear ribonucleoprotein particle
Department of Biochemistry and Institute of Human Genetics, University of Minnesota, Minneapolis, 55455, USA.
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