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Originally published In Press as doi:10.1074/jbc.M009105200 on May 4, 2001
J. Biol. Chem., Vol. 276, Issue 28, 25929-25938, July 13, 2001
Functional Organization of the GluR1 Glutamate Receptor
Promoter*
Karin
Borges and
Raymond
Dingledine
From the Department of Pharmacology, Emory University School of
Medicine, Atlanta, Georgia 30322
The GluR1 glutamate receptor subunit is expressed
in most brain areas and plays a major role in excitatory synaptic
transmission. We cloned and sequenced 5 kilobase pairs of the rat
GluR1 promoter and identified multiple transcriptional start
sites between 295 and 202 (relative to the first ATG). Similar to
other glutamate receptor subunit promoters, the GluR1 promoter lacks
TATA and CAAT elements in that region but binds Sp1 proteins at two
sites. Promoter activity of GluR1 fragments cloned into pGL3 was
assessed by immunocytochemistry and by measuring luciferase activity
after transfection into primary cultures of rat cortical neurons and glia. GluR1 promoter activity was stronger in neurons, with neuronal specificity appearing to reside mainly within the neuronal
expression-enhancing regions, 1395 to 743 and 253 to 48. The
latter region contains 4 sites that bound recombinant cAMP-response
element-binding proteins and a glial silencing region between 253 and
202. In both neurons and glia, promoter activity was increased by a
64-base pair GA repeat upstream of the initiation sites and reduced by
a 57-base pair region that contained an N box. In contrast to the GluR2 promoter the regulatory regions are mainly located outside of the GluR1
initiation region.
*
This work was supported in part by grants from the National
Institutes of Health.The costs of publication of this
article were defrayed in part by the
payment of page charges. The article must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AF302117.
Supported by the Deutsche Forschungsgemeinschaft and the Markey
Foundation. To whom correspondence should be addressed: Dept. of
Pharmacology, Emory University School of Medicine, 1510 Clifton Rd.,
Atlanta, GA 30322. Tel.: 404-727-5635; Fax: 404-727-0365; E-mail:
kborges@pharm.emory.edu.
Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.

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Copyright © 2001 by the American Society for Biochemistry and Molecular Biology.
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