Regulation of gene transcription in the gonadotrope is a key regulatory step that determines the levels of gonadotropin hormones and therefore, regulates gonadal function. Gametogenesis and steroidogenesis in both sexes are controlled by these two hormones, follicle-stimulating hormone (FSH) and luteinizing hormone (LH) from the pituitary, which are, in turn, regulated by gonadotropin-releasing hormone (GnRH) from the hypothalamus. GnRH regulates gonadotropin synthesis through induction of the three immediate early genes: ATF3 induces the ? glycoprotein subunit, Egr-1 induces the LH? subunit, and AP-1 induces the FSH? subunit. The overall goal of this application is to determine the GnRH-regulated transcriptomes comprised of these immediate early genes in the gonadotrope cell. We propose two complimentary aims to dissect transcriptional regulation from a more comprehensive standpoint. In the first aim, we will determine the complement of direct target genes, in addition to gonadotropin subunits, of these immediate early genes by ChIP-chip, which will allow us to delineate the transcriptional regulatory network. The intersection of genes that are induced by GnRH, already identified by expression array analysis, and the direct gene targets of these three most highly induced transcription factors determined herein by ChIP-chip, will focus our analysis on the most functional binding elements. Furthermore, overlap of these data sets will identify the genes whose transcription may be regulated similarly to gonadotropins. In the second aim, using a two-hybrid screen of a cDNA library from gonadotrope-derived cells, we will identify molecules that interact with ATF3, Egr-1 or AP-1, with a special emphasis on coactivators and corepressors. These cofactors may contribute to differential expression of the three gonadotropin subunits. Additionally, we will determine whether selected target genes from the first aim have similar sets of binding sites in their promoters and/or require the same cofactors, which may contribute to regulation of their expression. This approach will help us triangulate, from a broad perspective, the differential regulation of the gonadotropin subunits and whether it is accomplished by formation of diverse complexes on their respective promoters, in addition to analyzing the more global regulation of gene transcription in the gonadotrope. The results from this proposal will also open new avenues to study chromatin remodeling and activation of basal transcriptional machinery.

Public Health Relevance

Fertility in mammals is regulated by integration of different hormonal signals, which occurs at the level of the gonadotrope cell population in the pituitary gland. The integration ultimately results in the precisely orchestrated modulation of gene expression in the gonadotrope cell that leads to delicate balance of hormones that control reproduction. Thus, understanding the molecular mechanisms governing gonadotrope gene expression will lead to insight into the physiology and pathophysiology of the reproductive system.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21HD058752-01A1
Application #
7645442
Study Section
Integrative and Clinical Endocrinology and Reproduction Study Section (ICER)
Program Officer
Lamar, Charisee A
Project Start
2009-05-13
Project End
2011-04-30
Budget Start
2009-05-13
Budget End
2010-04-30
Support Year
1
Fiscal Year
2009
Total Cost
$231,750
Indirect Cost
Name
University of California San Diego
Department
Obstetrics & Gynecology
Type
Schools of Medicine
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Xie, Changchuan; Jonak, Carrie R; Kauffman, Alexander S et al. (2015) Gonadotropin and kisspeptin gene expression, but not GnRH, are impaired in cFOS deficient mice. Mol Cell Endocrinol 411:223-31
Roybal, Lacey L; Hambarchyan, Arpi; Meadows, Jason D et al. (2014) Roles of binding elements, FOXL2 domains, and interactions with cJUN and SMADs in regulation of FSH?. Mol Endocrinol 28:1640-55
Reddy, Gaddameedi R; Xie, Changchuan; Lindaman, Lacey L et al. (2013) GnRH increases c-Fos half-life contributing to higher FSH? induction. Mol Endocrinol 27:253-65
Lindaman, Lacey L; Yeh, Debra M; Xie, Changchuan et al. (2013) Phosphorylation of ATF2 and interaction with NFY induces c-Jun in the gonadotrope. Mol Cell Endocrinol 365:316-26
Breen, Kellie M; Thackray, Varykina G; Hsu, Tracy et al. (2012) Stress levels of glucocorticoids inhibit LH?-subunit gene expression in gonadotrope cells. Mol Endocrinol 26:1716-31
Ely, Heather A; Mellon, Pamela L; Coss, Djurdjica (2011) GnRH induces the c-Fos gene via phosphorylation of SRF by the calcium/calmodulin kinase II pathway. Mol Endocrinol 25:669-80
Thackray, Varykina G; Mellon, Pamela L; Coss, Djurdjica (2010) Hormones in synergy: regulation of the pituitary gonadotropin genes. Mol Cell Endocrinol 314:192-203
Corpuz, Patrick S; Lindaman, Lacey L; Mellon, Pamela L et al. (2010) FoxL2 Is required for activin induction of the mouse and human follicle-stimulating hormone beta-subunit genes. Mol Endocrinol 24:1037-51
Coss, Djurdjica; Mellon, Pamela L; Thackray, Varykina G (2010) A FoxL in the Smad house: activin regulation of FSH. Trends Endocrinol Metab 21:562-8
Breen, Kellie M; Thackray, Varykina G; Coss, Djurdjica et al. (2010) Runt-related transcription factors impair activin induction of the follicle-stimulating hormone {beta}-subunit gene. Endocrinology 151:2669-80

Showing the most recent 10 out of 12 publications