PMID- 20504961 OWN - NLM STAT- MEDLINE DCOM- 20100622 LR - 20240214 IS - 1477-9129 (Electronic) IS - 0950-1991 (Print) IS - 0950-1991 (Linking) VI - 137 IP - 13 DP - 2010 Jul TI - Specific roles of Target of rapamycin in the control of stem cells and their progeny in the Drosophila ovary. PG - 2117-26 LID - 10.1242/dev.050351 [doi] AB - Stem cells depend on intrinsic and local factors to maintain their identity and activity, but they also sense and respond to changing external conditions. We previously showed that germline stem cells (GSCs) and follicle stem cells (FSCs) in the Drosophila ovary respond to diet via insulin signals. Insulin signals directly modulate the GSC cell cycle at the G2 phase, but additional unknown dietary mediators control both G1 and G2. Target of rapamycin, or TOR, is part of a highly conserved nutrient-sensing pathway affecting growth, proliferation, survival and fertility. Here, we show that optimal TOR activity maintains GSCs but does not play a major role in FSC maintenance, suggesting differential regulation of GSCs versus FSCs. TOR promotes GSC proliferation via G2 but independently of insulin signaling, and TOR is required for the proliferation, growth and survival of differentiating germ cells. We also report that TOR controls the proliferation of FSCs but not of their differentiating progeny. Instead, TOR controls follicle cell number by promoting survival, independently of either the apoptotic or autophagic pathways. These results uncover specific TOR functions in the control of stem cells versus their differentiating progeny, and reveal parallels between Drosophila and mammalian follicle growth. FAU - LaFever, Leesa AU - LaFever L AD - Department of Cell and Developmental Biology, Vanderbilt University Medical Center, Nashville, TN 37232, USA. FAU - Feoktistov, Alexander AU - Feoktistov A FAU - Hsu, Hwei-Jan AU - Hsu HJ FAU - Drummond-Barbosa, Daniela AU - Drummond-Barbosa D LA - eng GR - R01 GM069875/GM/NIGMS NIH HHS/United States GR - T32 HD007043/HD/NICHD NIH HHS/United States GR - T32 HD007502/HD/NICHD NIH HHS/United States GR - T32HD007043/HD/NICHD NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't DEP - 20100526 PL - England TA - Development JT - Development (Cambridge, England) JID - 8701744 RN - 0 (Drosophila Proteins) RN - 0 (Insulin) RN - EC 2.7.- (Protein Kinases) RN - EC 2.7.1.- (target of rapamycin protein, Drosophila) RN - EC 2.7.11.1 (TOR Serine-Threonine Kinases) SB - IM EIN - Development. 2010 Jul;137(14):2451 MH - Animals MH - Cell Proliferation MH - Drosophila Proteins/*metabolism MH - Drosophila melanogaster/metabolism MH - Female MH - Insulin/metabolism MH - Ovary/cytology MH - Protein Kinases/*metabolism MH - Signal Transduction MH - Stem Cells/*metabolism MH - TOR Serine-Threonine Kinases PMC - PMC2882131 EDAT- 2010/05/28 06:00 MHDA- 2010/06/23 06:00 PMCR- 2011/07/01 CRDT- 2010/05/28 06:00 PHST- 2010/05/28 06:00 [entrez] PHST- 2010/05/28 06:00 [pubmed] PHST- 2010/06/23 06:00 [medline] PHST- 2011/07/01 00:00 [pmc-release] AID - dev.050351 [pii] AID - 10.1242/dev.050351 [doi] PST - ppublish SO - Development. 2010 Jul;137(13):2117-26. doi: 10.1242/dev.050351. Epub 2010 May 26.