scholarly journals Pit-1 Binding Sites at the Somatotrope-specific DNase I Hypersensitive Sites I, II of the Human Growth Hormone Locus Control Region Are Essential forin Vivo hGH-NGene Activation

1999 ◽  
Vol 274 (50) ◽  
pp. 35725-35733 ◽  
Author(s):  
Brian M. Shewchuk ◽  
Sylvia L. Asa ◽  
Nancy E. Cooke ◽  
Stephen A. Liebhaber
1995 ◽  
Vol 15 (12) ◽  
pp. 7010-7021 ◽  
Author(s):  
B K Jones ◽  
B R Monks ◽  
S A Liebhaber ◽  
N E Cooke

The five-member human growth hormone (hGH)/chorionic somatomammotropin (hCS) gene cluster encodes the pituitary-specific hGH-N gene and four highly related genes (hGH-V, hCS-A, hCS-B, and hCS-L) that are expressed only in the placenta. When the hGH-N or hCS-A gene, together with all previously identified cis-acting regulatory sequences, was integrated into the mouse genome, it was expressed only sporadically and at low levels in the transgenic target organs. DNase I mapping of chromatin from expressing and nonexpressing cell types was used to identify a pituitary-specific set of DNase I-hypersensitive sites (HS) and a set of HS common to both the pituitary and placenta, centered approximately 15 and 30 kb 5' of hGH-N, respectively. When contained on a cosmid insert in their native genomic configuration, these HS consistently directed high-level, pituitary-specific expression of hGH-N in transgenic mice and appeared to define a locus control region required for hGH-N expression. Individually, each set of HS was able to mediate position-independent hGH-N expression in the pituitary but demonstrated loss of physiologic control and loss of tissue specificity. The gene-proximal set of HS contained a potent enhancer activity in the pituitary, while the more distal set appeared to function primarily to establish site-of-integration independence. These data indicate that synergistic interactions among multiple elements are required to restrict hGH-N transcription to the pituitary and generate appropriate levels of expression. In addition, these results suggest a role for both shared and unique regulatory sequences in locus control region-mediated expression of the hGH/hCS gene cluster in the pituitary and possibly the placenta.


2012 ◽  
Vol 415 (1) ◽  
pp. 29-45 ◽  
Author(s):  
Tamra L. Hunsaker ◽  
Holly S. Jefferson ◽  
J. Kaitlin Morrison ◽  
Andrew J. Franklin ◽  
Brian M. Shewchuk

Haematologica ◽  
2015 ◽  
Vol 100 (5) ◽  
pp. e166-e168 ◽  
Author(s):  
A. Amid ◽  
M. Cheong ◽  
B. Eng ◽  
M. Hanna ◽  
B.-A. Hohenadel ◽  
...  

2006 ◽  
Vol 26 (17) ◽  
pp. 6535-6546 ◽  
Author(s):  
Brian M. Shewchuk ◽  
Yugong Ho ◽  
Stephen A. Liebhaber ◽  
Nancy E. Cooke

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.


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