The basic objective is to elucidate the molecular mechanisms involved in the regulation of expression of the proopiomelanocortin (POMC) gene in pituitary and hypothalamic tissues. Using a series of rat POMC-specific cDNAs and gene clones, we propose to further characterize the transcriptional regulation of the POMC gene by steroids, peptides, and catacholamines, both singlely and in combination. Some studies will be done in the intact animal; however, certain studies will be done in primary cultures of pituitary cells and in AtT20 tumor cells to preclude indirect effects on POMC gene expression. The exact sites in the POMC gene involved with regulation by specific hormones of gene expression will be mapped by deletion analysis and site directed mutagenesis. We have already constructed a rat POMC promoter/rat Prolactin coding region construct to aid in these studies. Using protein/DNA binding studies using the regions identified in the previous studies and a reinitiating nuclear transcription assay, we will begin to identify and characterize the transacting factors which mediate the peptide hormone, neurotransmitter, and steroid mediated modulation of POMC gene expression. In related studies, we will characterize the induction of the glucocorticoid receptor encoding gene after culturing of the intermediate lobe cells. In addition to understanding how expression of the glucocorticoid receptor gene is suppressed in the intact animal, these studies will allow us to develop a relatively homogeneous primary culture system in which we can study the glucocorticoid/CRF regulatory interactions. We will further characterize the regulation of the POMC gene system in the periarcuate region of the hypothalamus using several reproductive paradigms. Studies will be performed both by solution hybridization assays as well as in situ hybridization assays, coupled with several anatomical techniques to functionally subdivide the POMC neurons. We will further develop the use of POMC gene intervening sequence specific DNA probes in solution and in situ hybridization as an indirect method for analyzing transcriptional rates in small amounts of tissues and individual cells, respectively. These studies should yield a great deal of understanding of the complex interaction of various types of hormonal substances in the regulation of a specific gene in a complex but normal physiological situation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK027484-10
Application #
3228330
Study Section
Endocrinology Study Section (END)
Project Start
1987-08-01
Project End
1991-07-31
Budget Start
1989-08-01
Budget End
1990-07-31
Support Year
10
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Mount Sinai School of Medicine
Department
Type
Schools of Medicine
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10029
Boutillier, A L; Gaiddon, C; Lorang, D et al. (1998) Transcriptional activation of the proopiomelanocortin gene by cyclic AMP-responsive element binding protein. Pituitary 1:33-43
Boutillier, A L; Monnier, D; Lorang, D et al. (1995) Corticotropin-releasing hormone stimulates proopiomelanocortin transcription by cFos-dependent and -independent pathways: characterization of an AP1 site in exon 1. Mol Endocrinol 9:745-55
Han, E S; Levin, N; Bengani, N et al. (1995) Hyperadrenocorticism and food restriction-induced life extension in the rat: evidence for divergent regulation of pituitary proopiomelanocortin RNA and adrenocorticotropic hormone biosynthesis. J Gerontol A Biol Sci Med Sci 50:B288-94
Jin, W D; Boutillier, A L; Glucksman, M J et al. (1994) Characterization of a corticotropin-releasing hormone-responsive element in the rat proopiomelanocortin gene promoter and molecular cloning of its binding protein. Mol Endocrinol 8:1377-88
Levin, N; Wallace, C; Bengani, N et al. (1993) Ovine anterior pituitary proopiomelanocortin gene expression is not increased by ACTH secretagogues in vitro. Endocrinology 132:1692-700
Smith, A I; Levin, N; Wallace, C A et al. (1993) The role of vasopressin on ACTH secretion and biosynthesis in the ovine pituitary gland. Regul Pept 45:237-41
Boutillier, A L; Barthel, F; Roberts, J L et al. (1992) Beta-adrenergic stimulation of cFOS via protein kinase A is mediated by cAMP regulatory element binding protein (CREB)-dependent and tissue-specific CREB-independent mechanisms in corticotrope cells. J Biol Chem 267:23520-6
Mechanick, J I; Levin, N; Roberts, J L et al. (1992) Proopiomelanocortin gene expression in a distinct population of rat spleen and lung leukocytes. Endocrinology 131:518-25
Rasmussen, D D; Jakubowski, M; Allen, D L et al. (1992) Positive correlation between proopiomelanocortin and tyrosine hydroxylase mRNA levels in the mediobasohypothalamus of ovariectomized rats: response to estradiol replacement and withdrawal. Neuroendocrinology 56:285-94
Sheppard, K E; Roberts, J L; Blum, M (1991) Adrenocorticotropin-releasing factor down-regulates glucocorticoid receptor expression in mouse corticotrope tumor cells via an adenylate cyclase-dependent mechanism. Endocrinology 129:663-70

Showing the most recent 10 out of 24 publications