Affiliation:
1. Departments of Genetics
2. Medicine, The University of Pennsylvania, Philadelphia, Pennsylvania 19104
Abstract
ABSTRACT
Activation of the human growth hormone (
hGH-N
) gene in pituitary somatotropes is mediated by a locus control region (LCR). This LCR is composed of DNase I-hypersensitive sites (HS) located −14.5 kb to −32 kb relative to the
hGH-N
promoter. HSI, at −14.5 kb, is the dominant determinant of
hGH-N
expression and is essential for establishment of a 32-kb domain of histone acetylation that encompasses the active
hGH
locus. This activity is conferred by three binding sites for the POU domain transcription factor Pit-1. These Pit-1 elements are sufficient to activate
hGH-N
expression in the mouse pituitary. In contrast, Pit-1 sites at the
hGH-N
promoter are consistently unable to mediate similar activity. In the present study, we demonstrate that the functional difference between the promoter-proximal and the HSI Pit-1 binding sites can be attributed in part to a single base difference. This base affects the conformation of the Pit-1/DNA complex, and reciprocal exchange of the divergent bases between the two sets of Pit-1 elements results in a partial reversal of their transgenic activities. These data support a model in which the Pit-1 binding sites in the
hGH
LCR allosterically program the bound Pit-1 complex for chromatin activating functions.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
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