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PMID: 2840206 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Effects of RNA secondary structure on alternative splicing of pre-mRNA: is folding limited to a region behind the transcribing RNA polymerase?

Cell ·Vol. 54 ·No. 3 ·1988-07-29 ·Pages 393-401

Eperon LP, Graham IR, Griffiths AD, Eperon IC

Abstract

The use in vivo of an alternative 5' splice site sequestered within a short stem of potential RNA secondary structure is determined by the length of the loop. Above a threshold length of loop, the alternative site is used despite the potential structure. In contrast, the alternative site is used very little or not at all during splicing in vitro with all lengths of loop that we have tested. A model is proposed which suggests that pre-mRNA is free to fold only within a limited period after transcription.

MeSH Terms
Animals Cloning, Molecular DNA-Directed RNA Polymerases/metabolism Electrophoresis, Polyacrylamide Gel Endonucleases Exons Globins/genetics HeLa Cells Humans Models, Genetic Nucleic Acid Conformation RNA Precursors/genetics RNA Splicing RNA, Messenger/genetics Rabbits Single-Strand Specific DNA and RNA Endonucleases Transcription, Genetic
Chemicals
RNA Precursors RNA, Messenger Globins DNA-Directed RNA Polymerases Endonucleases Single-Strand Specific DNA and RNA Endonucleases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Eperon L P
Department of Biochemistry, University of Leicester, England.
Graham I R
Griffiths A D
Eperon I C
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1988-07-29
Pages
393-401
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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