Pitl, a tissue specific POU domain transcription factor that serves as a determining factor for three anterior pituitary cell types, was identified under this Award. Pit 1 regulates expression of many target genes, including growth hormone, prolactin, TSHalpha, and growth factor receptors including the growth hormone releasing factor receptor. This application proposes the definition of the molecular mechanisms by which the Pit 1 gene is initially activated and later exhibits auto regulation. Genetic, transgenic, and biochemical approaches will be used. The proposed studies include positional cloning of an informative regulatory locus and exploration of a novel pituitary HLH protein. The question of pituitary cell lineage will be investigated using contemporary gene rearrangement and transgenic technologies. Pit 1 acts in concert with other factors to determine cell specific patterns of gene expression, and the role of two novel homeodomain factors, Zn 15, and specific nuclear receptors in mediating the cell specific patterns of distal target gene expression will be studied. The possibility that novel co regulators of Pit 1 associate with distinct synergy domains in a gene specific fashion will be investigated. Current experiments that explore the role of the novel transcription factors in early pituitary development will be completed.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK018477-23
Application #
2684081
Study Section
Endocrinology Study Section (END)
Program Officer
Sato, Sheryl M
Project Start
1977-06-01
Project End
2001-03-31
Budget Start
1998-04-01
Budget End
1999-03-31
Support Year
23
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Kim, Hong Sook; Tan, Yuliang; Ma, Wubin et al. (2018) Pluripotency factors functionally premark cell-type-restricted enhancers in ES cells. Nature 556:510-514
Wang, Jianxun; Saijo, Kaoru; Skola, Dylan et al. (2018) Histone demethylase LSD1 regulates hematopoietic stem cells homeostasis and protects from death by endotoxic shock. Proc Natl Acad Sci U S A 115:E244-E252
Tan, Yuliang; Jin, Chunyu; Ma, Wubin et al. (2018) Dismissal of RNA Polymerase II Underlies a Large Ligand-Induced Enhancer Decommissioning Program. Mol Cell 71:526-539.e8
Cardamone, Maria Dafne; Tanasa, Bogdan; Cederquist, Carly T et al. (2018) Mitochondrial Retrograde Signaling in Mammals Is Mediated by the Transcriptional Cofactor GPS2 via Direct Mitochondria-to-Nucleus Translocation. Mol Cell 69:757-772.e7
Yang, Feng; Ma, Qi; Liu, Zhijie et al. (2017) Glucocorticoid Receptor:MegaTrans Switching Mediates the Repression of an ER?-Regulated Transcriptional Program. Mol Cell 66:321-331.e6
Puc, Janusz; Aggarwal, Aneel K; Rosenfeld, Michael G (2017) Physiological functions of programmed DNA breaks in signal-induced transcription. Nat Rev Mol Cell Biol 18:471-476
Puc, Janusz; Kozbial, Piotr; Li, Wenbo et al. (2015) Ligand-dependent enhancer activation regulated by topoisomerase-I activity. Cell 160:367-80
Li, Wenbo; Hu, Yiren; Oh, Soohwan et al. (2015) Condensin I and II Complexes License Full Estrogen Receptor ?-Dependent Enhancer Activation. Mol Cell 59:188-202
Wang, Jianxun; Telese, Francesca; Tan, Yuliang et al. (2015) LSD1n is an H4K20 demethylase regulating memory formation via transcriptional elongation control. Nat Neurosci 18:1256-64
Telese, Francesca; Ma, Qi; Perez, Patricia Montilla et al. (2015) LRP8-Reelin-Regulated Neuronal Enhancer Signature Underlying Learning and Memory Formation. Neuron 86:696-710

Showing the most recent 10 out of 61 publications