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Nat Struct Mol Biol. 2013 Jun;20(6):728-34. doi: 10.1038/nsmb.2556. Epub 2013 May 19.

A conformational switch in PRP8 mediates metal ion coordination that promotes pre-mRNA exon ligation.

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  • 1Department of Biochemistry, University of Alberta, Edmonton, Alberta, Canada.

Abstract

Splicing of pre-mRNAs in eukaryotes is catalyzed by the spliceosome, a large RNA-protein metalloenzyme. The catalytic center of the spliceosome involves a structure comprising the U2 and U6 snRNAs and includes a metal bound by U6 snRNA. The precise architecture of the splicesome active site, however, and the question of whether it includes protein components, remains unresolved. A wealth of evidence places the protein PRP8 at the heart of the spliceosome through assembly and catalysis. Here we provide evidence that the RNase H domain of PRP8 undergoes a conformational switch between the two steps of splicing, rationalizing yeast prp8 alleles that promote either the first or second step. We also show that this switch unmasks a metal-binding site involved in the second step. Together, these data establish that PRP8 is a metalloprotein that promotes exon ligation within the spliceosome.

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PMID:
23686287
PMCID:
PMC3703396
DOI:
10.1038/nsmb.2556
[PubMed - indexed for MEDLINE]
Free PMC Article
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