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Short artificial hairpins sequester splicing signals and inhibit yeast pre-mRNA splicing.
Author(s) -
Valérie Goguel,
Y. Lynn Wang,
Michael Rosbash
Publication year - 1993
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.13.11.6841
Subject(s) - rna splicing , spliceosome , biology , protein splicing , prp24 , polypyrimidine tract , exonic splicing enhancer , saccharomyces cerevisiae , precursor mrna , ribonucleoprotein , microbiology and biotechnology , sr protein , small nuclear ribonucleoprotein , rna , genetics , yeast , gene
To examine the stability of yeast (Saccharomyces cerevisiae) pre-mRNA structures, we inserted a series of small sequence elements that generated potential RNA hairpins at the 5' splice site and branch point regions. We analyzed spliceosome assembly and splicing in vitro as well as splicing and nuclear pre-mRNA retention in vivo. Surprisingly, the inhibition of in vivo splicing approximately paralleled that of in vitro splicing. Even a 6-nucleotide hairpin could be shown to inhibit splicing, and a 15-nucleotide hairpin gave rise to almost complete inhibition. The in vitro results indicate that hairpins that sequester the 5' splice site have a major effect on the early steps of spliceosome assembly, including U1 small nuclear ribonucleoprotein binding. The in vivo experiments lead to comparable conclusions as the sequestering hairpins apparently result in the transport of pre-mRNA to the cytoplasm. The observations are compared with previous data from both yeast and mammalian systems and suggest an important effect of pre-mRNA structure on in vivo splicing.

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