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PMID: 3021333 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

One binding site determines sequence specificity of Tetrahymena pre-rRNA self-splicing, trans-splicing, and RNA enzyme activity.

Cell ·Vol. 47 ·No. 2 ·1986-10-24 ·Pages 207-16

Been MD, Cech TR

Abstract

The specificity of reactions catalyzed by the Tetrahymena pre-rRNA intervening sequence (IVS) was studied using site-specific mutagenesis. Two sequences required for 5' splice-site selection during self-splicing were defined. Single-base changes in either a 5' exon sequence or a 5' exon-binding site within the IVS disrupt their ability to pair and result in inefficient or inaccurate splicing. Combinations that restore complementarity suppress the effect of the single-base changes. Sequence alterations in the 5' exon-binding site also change the specificity of two other reactions: intermolecular exon ligation (trans-splicing) and the enzymatic nucleotidyltransferase activity of the IVS RNA. Thus the substrate specificity of an RNA enzyme can be changed in a manner predictable by the rules of Watson-Crick base-pairing.

MeSH Terms
Base Sequence Binding Sites Exons Guanosine Triphosphate/metabolism Introns Mutation Nucleic Acid Conformation Nucleotidyltransferases/metabolism RNA Splicing RNA, Ribosomal/genetics Substrate Specificity Templates, Genetic Tetrahymena/physiology
Chemicals
RNA, Ribosomal Guanosine Triphosphate Nucleotidyltransferases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Been M D
Cech T R
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1986-10-24
Pages
207-16
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIGMS NIH HHS · GM28039 · United States
Databases
GENBANK
M14748
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