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J. Biol. Chem., Vol. 276, Issue 28, 25929-25938, July 13, 2001
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and
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.
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.
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