help button home button Endocrine Society Molecular Endocrinology ENDO 08 Sessions Library
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Pennathur, S.
Right arrow Articles by Jameson, J. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Pennathur, S.
Right arrow Articles by Jameson, J. L.

Molecular Endocrinology, Vol 7, 797-805, Copyright © 1993 by Endocrine Society


ARTICLES

Localization of promoter sequences required for thyrotropin-releasing hormone and thyroid hormone responsiveness of the glycoprotein hormone alpha-gene in primary cultures of rat pituitary cells

S Pennathur, LD Madison, TW Kay and JL Jameson
Thyroid Unit, Massachusetts General Hospital, Harvard Medical School, Boston 02114.

The glycoprotein hormone alpha-gene is regulated by multiple hormones in different pituitary and placental cell types. In thyrotropes, the alpha-gene is stimulated by TRH and repressed by thyroid hormone (T3). We used transient expression assays in primary cultures of rat pituitary cells to examine regulation of the alpha-promoter (alpha Luc) by TRH and T3. The -846 alpha Luc activity was stimulated 3.4-fold by TRH and repressed 44% by T3. GnRH and cAMP stimulated -846 alpha Luc by 8.3- and 8.6-fold, respectively. T3 blocked TRH stimulation, but it had no effect on stimulation by GnRH or cAMP, suggesting that the T3- mediated effects are thyrotrope specific. TRH and T3 responsiveness was preserved with deletions to -346 basepairs (bp). TRH responsiveness was lost after deletion to -280 bp, whereas T3-mediated repression was eliminated by further deletion to -180 bp. A series of DNA fragments between -420 and -180 was linked to -132 alpha Luc to study TRH and T3 responses in greater detail. Sequences between -346 to -180 bp conferred TRH responsiveness and T3 inhibition. TRH responsiveness was not seen after 3'-deletions of this fragment to -244 or -280 bp. These results together with the 5'-deletions provide evidence for two interdependent TRH regulatory regions: one between -346 to -280 bp and another between -244 to -180 bp. T3-dependent repression only requires sequences between -244 and -180 bp. Site-directed cluster mutations were created in each of these two regulatory domains. A mutation in region 1 (-346 to -328 bp) eliminated TRH stimulation, but retained basal suppression by T3.(ABSTRACT TRUNCATED AT 250 WORDS)


This article has been cited by other articles:


Home page
EndocrinologyHome page
M. I. Chiamolera and F. E. Wondisford
Thyrotropin-Releasing Hormone and the Thyroid Hormone Feedback Mechanism
Endocrinology, March 1, 2009; 150(3): 1091 - 1096.
[Abstract] [Full Text] [PDF]


Home page
Endocr. Rev.Home page
J. S. Jorgensen, C. C. Quirk, and J. H. Nilson
Multiple and Overlapping Combinatorial Codes Orchestrate Hormonal Responsiveness and Dictate Cell-Specific Expression of the Genes Encoding Luteinizing Hormone
Endocr. Rev., August 1, 2004; 25(4): 521 - 542.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
E. J. Lee, L. M. Anderson, B. Thimmapaya, and J. L. Jameson
Targeted Expression of Toxic Genes Directed by Pituitary Hormone Promoters: A Potential Strategy for Adenovirus-Mediated Gene Therapy of Pituitary Tumors
J. Clin. Endocrinol. Metab., February 1, 1999; 84(2): 786 - 794.
[Abstract] [Full Text]


Home page
EndocrinologyHome page
B. Yusta, E. T. Alarid, D. F. Gordon, E. C. Ridgway, and P. L. Mellon
The Thyrotropin {beta}-Subunit Gene Is Repressed by Thyroid Hormone in a Novel Thyrotrope Cell Line, Mouse T{alpha}T1 Cells
Endocrinology, November 1, 1998; 139(11): 4476 - 4482.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
I. M. Colin and J. L. Jameson
Estradiol Sensitization of Rat Pituitary Cells to Gonadotropin-Releasing Hormone: Involvement of Protein Kinase C- and Calcium-Dependent Signaling Pathways
Endocrinology, September 1, 1998; 139(9): 3796 - 3802.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
S. Chin, J. Apriletti, and G. Gick
Characterization of a Negative Thyroid Hormone Response Element in the Rat Sodium, Potassium-Adenosine Triphosphatase {alpha}3 Gene Promoter
Endocrinology, August 1, 1998; 139(8): 3423 - 3431.
[Abstract] [Full Text] [PDF]


Home page
Mol. Endocrinol.Home page
M. L. Brinkmeier, D. F. Gordon, J. M. Dowding, T. L. Saunders, S. K. Kendall, V. D. Sarapura, W. M. Wood, E. C. Ridgway, and S. A. Camper
Cell-Specific Expression of the Mouse Glycoprotein Hormone {alpha}-Subunit Gene Requires Multiple Interacting DNA Elements in Transgenic Mice and Cultured Cells
Mol. Endocrinol., May 1, 1998; 12(5): 622 - 633.
[Abstract] [Full Text]


Home page
J. Clin. Endocrinol. Metab.Home page
D. P. Olson and R. J. Koenig
Thyroid Function in Rubinstein-Taybi Syndrome
J. Clin. Endocrinol. Metab., October 1, 1997; 82(10): 3264 - 3266.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
K. Hashimoto, K. Zanger, A. N. Hollenberg, L. E. Cohen, S. Radovick, and F. E. Wondisford
cAMP Response Element-binding Protein-binding Protein Mediates Thyrotropin-releasing Hormone Signaling on Thyrotropin Subunit Genes
J. Biol. Chem., October 20, 2000; 275(43): 33365 - 33372.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 1993 by The Endocrine Society