(Hypertension. 1996;27:1018-1024.)
© 1996 American Heart Association, Inc.
Articles |
2A-Adrenergic Receptor Gene
From the Hypertension and Atherosclerosis Section, Department of Medicine, Boston University School of Medicine (Mass).
Correspondence to Diane E. Handy, W520, Boston University School of Medicine, 80 E Concord St, Boston, MA 02118.
Abstract We investigated the transcriptional activity of the
-131 to -92 region of the rat
2A-adrenergic
receptor gene. In HT29 cells, this region has a positive effect on
transcription, whereas in RINm5F cells, this region has a negative
effect on transcription. The -131 to -92 region has a GC
box (GGGGCGG) surrounded by overlapping GGAGG repeats. To
analyze nuclear factor binding to this region, we made a series
of sequence substitutions in the GGAGG repeats, the GC box, or both
regions. Gel mobility shift assays indicated that most of the nuclear
factor complexes formed between the wild-type -131/-92
sequence and either HT29 or RINm5F extracts were specific for Sp1 or
related proteins that recognize a GC box. Mutation of either the GGAGG
repeats or the GC box did not eliminate the binding of Sp1 or related
nuclear factors, suggesting that both the GGAGG repeats and the GC box
could bind Sp1-related factors. Mutation of both these sites eliminated
the binding of Sp1-related factors. In the absence of Sp1 binding
sites, this region had a negative effect on transcription in HT29 and a
positive effect on transcription in RINm5F cells. These data support
the notion that Sp1 and/or a related factor may control both positive
and negative gene expression and suggest that the -131/-92
region may be involved in regulating tissue-specific levels of
2A-adrenergic receptor gene expression.
Key Words: receptors, adrenergic, alpha transcription, genetic molecular biology
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