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PMID: 8500172 Published · ppublish English Journal Article

3' splice site recognition in S. cerevisiae does not require base pairing with U1 snRNA.

Cell ·Vol. 73 ·No. 4 ·1993-05-21 ·Pages 803-12

Séraphin B, Kandels-Lewis S

Abstract

The conserved nucleotides 9 and 10 of U1 small nuclear RNA (snRNA) have been proposed to base pair with either 5' exon or 3' splice site sequences. In S. pombe, U1 snRNA pairing with the conserved 3' splice site is required for the first step of splicing and viability. In contrast, we show that S. cerevisiae U1 mutants at positions 9 and 10 are fully functional. Splicing of several genes is normal in these strains, ruling out an essential base pairing between U1 snRNA and 3' splice sites. U1 snRNA positions 9 and 10 are shown to be involved in 5' splice site selection through their interaction with exon sequences. Our results demonstrate that some snRNA-pre-mRNA interactions are not evolutionarily conserved and that 3' splice site recognition occurs by different mechanisms in various organisms.

MeSH Terms
Base Sequence Biological Evolution Exons Molecular Sequence Data Mutation Nucleic Acid Hybridization RNA Splicing/physiology RNA, Fungal/physiology RNA, Small Nuclear/physiology Ribonucleoprotein, U1 Small Nuclear/physiology Saccharomyces cerevisiae/genetics
Chemicals
RNA, Fungal RNA, Small Nuclear Ribonucleoprotein, U1 Small Nuclear
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Séraphin B
European Molecular Biology Laboratory, Heidelberg, Federal Republic of Germany.
Kandels-Lewis S
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1993-05-21
Pages
803-12
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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