Our long-term goal is to understand the developmental and molecular basis for interactions that influence germline proliferation and differentiation. The germ cells of most animals, including mammals, proliferate extensively during development. This expansion is required to produce an adequate progenitor pool for adult gamete production. In addition to cell cycle progression, these cells must resist differentiation that would remove them from the proliferating state. We are investigating how nutritionally-sensitive signaling pathways control the accumulation and maintenance of the proliferating germ cells. These mechanisms are best studied in a whole-organism context that is amenable to genetic and molecular analysis, such as the nematode C. elegans. Recent studies from our lab implicate the highly conserved TOR target S6 kinase (S6K) in the control of germline proliferation and differentiation in C. elegans. Using complementary molecular-genetic and biochemical approaches, we propose to identify and characterize the relevant targets of S6K for its roles in regulating germline proliferation, differentiation, and sensitivity to organisal nutrition. Despite the evolutionary distance between C. elegans and mammals, this kinase is highly conserved. Therefore, these studies will likely provide broadly applicable results and lend insights into S6K function in other systems. Our studies will also shed light on general mechanisms that control the expansion of proliferating cell populations, with implications for fertility, development, cancer, and stem cell biology.

Public Health Relevance

Germ cells are the link from generation to generation and must proliferate and differentiate properly to ensure fertility. Germ cell proliferation and differentiation is controlled by interaction with neighboring cells, by hormones, and by nutrition. We study conserved molecular pathways that control germ cell proliferation and differentiation, as well as sensitivity to nutrition. These investigations inform similar processes in humans with general implications for fertility, cancer, and stem cell biology.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM061706-14
Application #
8987699
Study Section
Special Emphasis Panel (ZRG1-EMNR-D (02))
Program Officer
Gaillard, Shawn R
Project Start
2000-07-01
Project End
2019-05-31
Budget Start
2015-09-15
Budget End
2016-05-31
Support Year
14
Fiscal Year
2015
Total Cost
$367,391
Indirect Cost
$150,641
Name
New York University
Department
Pathology
Type
Schools of Medicine
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
Roy, Debasmita; Kahler, David J; Yun, Chi et al. (2018) Functional Interactions Between rsks-1/S6K, glp-1/Notch, and Regulators of Caenorhabditis elegans Fertility and Germline Stem Cell Maintenance. G3 (Bethesda) 8:3293-3309
McGovern, Marie; Castaneda, Perla Gisela; Pekar, Olga et al. (2018) The DSL ligand APX-1 is required for normal ovulation in C. elegans. Dev Biol 435:162-169
Pekar, Olga; Ow, Maria C; Hui, Kailyn Y et al. (2017) Linking the environment, DAF-7/TGF? signaling and LAG-2/DSL ligand expression in the germline stem cell niche. Development 144:2896-2906
Atwell, Kathryn; Dunn, Sara-Jane; Osborne, James M et al. (2016) How computational models contribute to our understanding of the germ line. Mol Reprod Dev 83:944-957
Roy, Debasmita; Michaelson, David; Hochman, Tsivia et al. (2016) Cell cycle features of C. elegans germline stem/progenitor cells vary temporally and spatially. Dev Biol 409:261-271
Atwell, Kathryn; Qin, Zhao; Gavaghan, David et al. (2015) Mechano-logical model of C. elegans germ line suggests feedback on the cell cycle. Development 142:3902-11
Deng, Xinzhu; Michaelson, David; Tchieu, Jason et al. (2015) Targeting Homologous Recombination in Notch-Driven C. elegans Stem Cell and Human Tumors. PLoS One 10:e0127862
Qin, Zhao; Hubbard, E Jane Albert (2015) Non-autonomous DAF-16/FOXO activity antagonizes age-related loss of C. elegans germline stem/progenitor cells. Nat Commun 6:7107
Hubbard, E Jane Albert (2014) FLP/FRT and Cre/lox recombination technology in C. elegans. Methods 68:417-24
Hubbard, E Jane Albert; Korta, Dorota Z; Dalfó, Diana (2013) Physiological control of germline development. Adv Exp Med Biol 757:101-31

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