Our long term goal is to learn how the self-renewing asymmetric division of stem cells is achieved, a question crucial to the understanding of tissue development/repair, oncogenesis, immunodeficiency, and sterility. Our focus has been to address this question in Drosophila germline stem cells, initially by identifying these cells and revealing the self-renewing asymmetry of their division, followed by genetic dissection of the underlying mechanism. This leads to the finding of piwi, Yb, pumilio (pum), and arrest (aret) genes essential for germline stem cell renewal. Our working hypothesis is that the self- renewing ability of germ-line stem cells is induced by signaling from Yb/piwi/hh-expressing apical somatic cells. The somatic induction is achieved by controlling the asymmetric distribution of key proteins between the stem cell and its differentiated daughter, the cystoblast, which renders their specific fates. Such key proteins include PUM which regulates differential translation, BAM which promotes cystoblast differentiation and PIWI which is also expressed in the germline as a cell-autonomous promoter of stem cell division.
Our specific aims are to explore the stem cell mechanism by systematically testing and expanding this hypothesis. With all the tools in place and experience in most of the following analyses, we propose to: 1. Analyze the biochemical role of PIWI as a nuclear factor in germline stem cell division. 2. Examine the developmental role of Yb in signaling germline stem cell division. 3. Analyze the biochemical role of YB in signaling cells. 4. Define regulatory relationship between genes involved in producing somatic signals. 5. Identify new genes interacting with piwi by genetic suppressor screens.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD033760-07
Application #
6499083
Study Section
Genetics Study Section (GEN)
Program Officer
Tasca, Richard J
Project Start
1996-02-01
Project End
2005-01-31
Budget Start
2002-02-01
Budget End
2003-01-31
Support Year
7
Fiscal Year
2002
Total Cost
$342,222
Indirect Cost
Name
Duke University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Ge, Xin Quan; Han, Jinah; Cheng, Ee-Chun et al. (2015) Embryonic Stem Cells License a High Level of Dormant Origins to Protect the Genome against Replication Stress. Stem Cell Reports 5:185-94
Mani, Sneha Ramesh; Megosh, Heather; Lin, Haifan (2014) PIWI proteins are essential for early Drosophila embryogenesis. Dev Biol 385:340-9
Huang, Xiao Albert; Lin, Haifan (2012) The miRNA Regulation of Stem Cells. Wiley Interdiscip Rev Membr Transp Signal 1:83-95
Huang, Xiao Albert; Lin, Haifan (2012) The microRNA regulation of stem cells. Wiley Interdiscip Rev Dev Biol 1:83-95
Yin, Hang; Sweeney, Sarah; Raha, Debasish et al. (2011) A high-resolution whole-genome map of key chromatin modifications in the adult Drosophila melanogaster. PLoS Genet 7:e1002380
Liu, Li; Qi, Hongying; Wang, Jianquan et al. (2011) PAPI, a novel TUDOR-domain protein, complexes with AGO3, ME31B and TRAL in the nuage to silence transposition. Development 138:1863-73
Gangaraju, Vamsi K; Yin, Hang; Weiner, Molly M et al. (2011) Drosophila Piwi functions in Hsp90-mediated suppression of phenotypic variation. Nat Genet 43:153-8
Juliano, Celina; Wang, Jianquan; Lin, Haifan (2011) Uniting germline and stem cells: the function of Piwi proteins and the piRNA pathway in diverse organisms. Annu Rev Genet 45:447-69
Qi, Hongying; Watanabe, Toshiaki; Ku, Hsueh-Yen et al. (2011) The Yb body, a major site for Piwi-associated RNA biogenesis and a gateway for Piwi expression and transport to the nucleus in somatic cells. J Biol Chem 286:3789-97
Smulders-Srinivasan, Tora K; Szakmary, Akos; Lin, Haifan (2010) A Drosophila chromatin factor interacts with the Piwi-interacting RNA mechanism in niche cells to regulate germline stem cell self-renewal. Genetics 186:573-83

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