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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