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PMID: 3848348 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Trans splicing of mRNA precursors in vitro.

Cell ·Vol. 42 ·No. 1 ·1985-08-00 ·Pages 165-71

Konarska MM, Padgett RA, Sharp PA

Abstract

Two exon segments from two separate RNA molecules can be joined in a trans splicing process. In trans splicing reactions, an RNA molecule containing an exon, a 5' splice site, and adjacent intron sequences was mixed with an RNA molecule containing an exon, a 3' splice site, and adjacent intron sequences. The efficiency of trans splicing of these two RNAs increased if the two termini of the intervening sequences were paired in a short RNA duplex. However, trans splicing of two RNA molecules with no significant complementarity was also observed. These results strongly suggest that significant secondary structures within intervening sequences could affect the splicing of flanking exons. Similarly, RNAs that are complementary to segments within the intervening sequences could potentially regulate the selection of splice sites. Finally, some organisms might use trans splicing to distribute a single exon to many different mRNAs.

MeSH Terms
Adenosine Triphosphate/pharmacology Adenoviruses, Human/genetics Base Sequence Nucleic Acid Hybridization Nucleic Acid Precursors/metabolism RNA Precursors RNA Splicing RNA, Messenger/metabolism RNA, Viral/metabolism Transcription, Genetic
Chemicals
Nucleic Acid Precursors RNA Precursors RNA, Messenger RNA, Viral Adenosine Triphosphate
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Konarska M M
Padgett R A
Sharp P A
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1985-08-00
Pages
165-71
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NCI NIH HHS · P01-CA14051 · United States
NCI NIH HHS · P01-CA26717 · United States
NIGMS NIH HHS · R01-GM32467 · United States
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