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J Biol Chem, Vol. 274, Issue 12, 7893-7900, March 19, 1999
Isolation and Characterization of a Novel Promoter for the Bovine
Growth Hormone Receptor Gene
Honglin
Jiang,
Carol S.
Okamura, and
Matthew C.
Lucy
From the Department of Animal Sciences, University of Missouri,
Columbia, Missouri 65211
The use of alternative promoters represents an
important mechanism for the regulation of growth hormone receptor (GHR)
gene expression. Two promoters have been isolated previously for the GHR gene: the P1 promoter that drives liver-specific expression, and
the P2 promoter that drives ubiquitous expression. In the present
study, we isolated a third GHR promoter termed P3. The P3 promoter was
GC-rich and TATA-less. The P3 promoter was able to drive the expression
of a luciferase reporter gene in cell lines Hep G2, PLC/PRF/5, and
BHK-21. In vivo, the P3 promoter initiated transcription
from two major sites in exon 1C of the GHR gene in many tissues. In the
adult bovine liver, the P3-transcribed GHR mRNA represented only
10% of the total GHR mRNA pool. In non-hepatic tissues such as
kidney, skeletal muscle, mammary gland, and uterus, P3-transcribed GHR
mRNA represented 30-40% of the total GHR mRNA pool. Within
the bovine GHR gene, the P3 promoter was located immediately downstream
from the P2 promoter. In transfected cells, the P2 promoter served as
an enhancer for the P3 promoter. Existence and co-regulation of two
ubiquitous promoters may be a mechanism for achieving a high level of
expression of the GHR gene in multiple tissues.
Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.

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Copyright © 1999 by the American Society for Biochemistry and Molecular Biology.
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