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PMID: 8700852 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Q/R site editing in kainate receptor GluR5 and GluR6 pre-mRNAs requires distant intronic sequences.

Herb A, Higuchi M, Sprengel R, Seeburg PH

Abstract

RNA editing by adenosine deamination in brain-expressed pre-mRNAs for glutamate receptor (GluR) subunits alters gene-specified codons for functionally critical positions, such as the channel's Q/R site. We show by transcript analysis of minigenes transiently expressed in PC-12 cells that, in contrast to GluR-B pre-mRNA, where the two editing sites (Q/R and R/G) require base pairing with nearby intronic editing site complementary sequences (ECSs), editing in GluR5 and GluR6 pre-mRNAs recruits an ECS located as far as 1900 nucleotides distal to the Q/R site. The exon-intron duplex structure of the GluR5 and GluR6 pre-mRNAs appears to be a substrate of double-stranded RNA-specific adenosine deaminase. This enzyme when coexpressed in HEK 293 cells preferentially targets the adenosine of the Q/R site and of an unpaired position in the ECS which is highly edited in brain.

MeSH Terms
Adenosine/chemistry Amino Acid Sequence Animals Base Sequence Brain/physiology DNA Primers/chemistry Hydrogen Bonding Introns Mice Molecular Sequence Data Nucleic Acid Conformation PC12 Cells RNA Editing RNA Precursors RNA, Double-Stranded/genetics Rats Receptors, Kainic Acid/genetics
Chemicals
DNA Primers RNA Precursors RNA, Double-Stranded Receptors, Kainic Acid Adenosine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Herb A
Laboratory for Molecular Neuroendocrinololgy, Zentrum für Molekulare Biologie, Heidelberg, Germany.
Higuchi M
Sprengel R
Seeburg P H
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1996-03-05
Pages
1875-80
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC39875
Subset
IM
Databases
GENBANK
U31443, U31444
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