Inducible somatic oocyte destruction in response to rapamycin requires wild-type regulation of follicle cell epithelial polarity

T C Thomson; J Johnson

doi:10.1038/cdd.2010.49

journal article May 07, 2010

Inducible somatic oocyte destruction in response to rapamycin requires wild-type regulation of follicle cell epithelial polarity

T C Thomson J Johnson

Cell Death & Differentiation Vol. 17 No. 11 pp. 1717-1727 · Springer Science and Business Media LLC

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References

40

[1]

Mouse Ovarian Germ Cell Cysts Undergo Programmed Breakdown to Form Primordial Follicles

Melissa E. Pepling, Allan C. Spradling

Developmental Biology 2001 10.1006/dbio.2001.0269

[2]

Pepling ME . From primordial germ cell to primordial follicle: mammalian female germ cell development. Genesis 2006; 44: 622–632. 10.1002/dvg.20258

[3]

Noce T, Okamoto-Ito S, Tsunekawa N . Vasa homolog genes in mammalian germ cell development. Cell Struct Funct 2001; 26: 131–136. 10.1247/csf.26.131

[4]

Baskind HA, Na L, Ma Q, Patel MP, Geenen DL, Wang QT . Functional conservation of asxl2, a murine homolog for the Drosophila enhancer of trithorax and polycomb group gene asx. PLoS One 2009; 4: e4750. 10.1371/journal.pone.0004750

[5]

Mazzalupo S, Cooley L . Illuminating the role of caspases during Drosophila oogenesis. Cell Death Differ 2006; 13: 1950–1959. 10.1038/sj.cdd.4401892

[6]

INVOLVEMENT OF APOPTOSIS IN OVARIAN FOLLICULAR ATRESIA AND POSTOVULATORY REGRESSION

Jonathan L. Tilly, Kim I. Kowalski, Alan L. Johnson et al.

Endocrinology 1991 10.1210/endo-129-5-2799

[7]

Tilly JL . Molecular and genetic basis of normal and toxicant-induced apoptosis in female germ cells. Toxicol Lett 1998; 102–103: 497–501. 10.1016/s0378-4274(98)00240-9

[8]

Lobascio AM, Klinger FG, Scaldaferri ML, Farini D, De Felici M . Analysis of programmed cell death in mouse fetal oocytes. Reproduction 2007; 134: 241–252. 10.1530/rep-07-0141

[9]

Escobar ML, Echeverra OM, Ortz R, Vzquez-Nin GH . Combined apoptosis and autophagy, the process that eliminates the oocytes of atretic follicles in immature rats. Apoptosis 2008; 13: 1253–1266. 10.1007/s10495-008-0248-z

[10]

Inoue S, Watanabe H, Saito H, Hiroi M, Tonosaki A . Elimination of atretic follicles from the mouse ovary: a tem and immunohistochemical study in mice. J Anat 2000; 196 (Part 1): 103–110. 10.1046/j.1469-7580.2000.19610103.x

[11]

Drummond-Barbosa D, Spradling AC . Stem cells and their progeny respond to nutritional changes during Drosophila oogenesis. Dev Biol 2001; 231: 265–278. 10.1006/dbio.2000.0135

[12]

LaFever L, Drummond-Barbosa D . Direct control of germline stem cell division and cyst growth by neural insulin in Drosophila. Science 2005; 309: 1071–1073. 10.1126/science.1111410

[13]

Pritchett TL, Tanner EA, McCall K . Cracking open cell death in the Drosophila ovary. Apoptosis 2009; 14: 969–979. 10.1007/s10495-009-0369-z

[14]

Gingras AC, Raught B, Sonenberg N . Regulation of translation initiation by FRAP/mTOR. Genes Dev 2001; 15: 807–826. 10.1101/gad.887201

[15]

Wiederrecht GJ, Sabers CJ, Brunn GJ, Martin MM, Dumont FJ, Abraham RT . Mechanism of action of rapamycin: new insights into the regulation of g1-phase progression in eukaryotic cells. Prog Cell Cycle Res 1995; 1: 53–71. 10.1007/978-1-4615-1809-9_5

[16]

TOR Signaling in Growth and Metabolism

Stephan Wullschleger, Robbie Loewith, Michael N. Hall

Cell 2006 10.1016/j.cell.2006.01.016

[17]

Mammalian TOR complex 2 controls the actin cytoskeleton and is rapamycin insensitive

Estela Jacinto, Robbie Loewith, Anja Schmidt et al.

Nature Cell Biology 2004 10.1038/ncb1183

[18]

Harrar Y, Bellini C, Faure JD . Fkbps: at the crossroads of folding and transduction. Trends Plant Sci 2001; 6: 426–431. 10.1016/s1360-1385(01)02044-1

[19]

Zhang H, Stallock JP, Ng JC, Reinhard C, Neufeld TP . Regulation of cellular growth by the Drosophila target of rapamycin dTOR. Genes Dev 2000; 14: 2712–2724. 10.1101/gad.835000

[20]

Prasad M, Jang AC, Starz-Gaiano M, Melani M, Montell DJ . A protocol for culturing Drosophila melanogaster stage 9 egg chambers for live imaging. Nat Protoc 2007; 2: 2467–2473. 10.1038/nprot.2007.363

[21]

Wang X, Proud CG . Nutrient control of TORC1, a cell-cycle regulator. Trends Cell Biol 2009; 19: 260–267. 10.1016/j.tcb.2009.03.005

[22]

Brand AH, Perrimon N . Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development 1993; 118: 401–415. 10.1242/dev.118.2.401

[23]

Van Doren M, Williamson AL, Lehmann R . Regulation of zygotic gene expression in Drosophila primordial germ cells. Curr Biol 1998; 8: 243–246. 10.1016/s0960-9822(98)70091-0

[24]

Kennerdell JR, Yamaguchi S, Carthew RW . RNAi is activated during Drosophila oocyte maturation in a manner dependent on aubergine and spindle-E. Genes Dev 2002; 16: 1884–1889. 10.1101/gad.990802

[25]

Zhang Y, Billington CJ, Pan D, Neufeld TP . Drosophila target of rapamycin kinase functions as a multimer. Genetics 2006; 172: 355–362. 10.1534/genetics.105.051979

[26]

Udan RS, Kango-Singh M, Nolo R, Tao C, Halder G . Hippo promotes proliferation arrest and apoptosis in the Salvador/Warts pathway. Nat Cell Biol 2003; 5: 914–920. 10.1038/ncb1050

[27]

Polesello C, Tapon N . Salvador-warts-hippo signaling promotes Drosophila posterior follicle cell maturation downstream of notch. Curr Biol 2007; 17: 1864–1870. 10.1016/j.cub.2007.09.049

[28]

Meignin C, Alvarez-Garcia I, Davis I, Palacios IM . The salvador-warts-hippo pathway is required for epithelial proliferation and axis specification in Drosophila. Curr Biol 2007; 17: 1871–1878. 10.1016/j.cub.2007.09.062

[29]

Hamaratoglu F, Willecke M, Kango-Singh M, Nolo R, Hyun E, Tao C et al. The tumour-suppressor genes NF2/Merlin and expanded act through hippo signalling to regulate cell proliferation and apoptosis. Nat Cell Biol 2006; 8: 27–36. 10.1038/ncb1339

[30]

MacDougall N, Lad Y, Wilkie GS, Francis-Lang H, Sullivan W, Davis I . Merlin, the Drosophila homologue of neurofibromatosis-2, is specifically required in posterior follicle cells for axis formation in the oocyte. Development 2001; 128: 665–673. 10.1242/dev.128.5.665

[31]

LaJeunesse DR, McCartney BM, Fehon RG . Structural analysis of Drosophila merlin reveals functional domains important for growth control and subcellular localization. J Cell Biol 1998; 141: 1589–1599. 10.1083/jcb.141.7.1589

[32]

Zhao M, Szafranski P, Hall CA, Goode S . Basolateral junctions utilize warts signaling to control epithelial-mesenchymal transition and proliferation crucial for migration and invasion of Drosophila ovarian epithelial cells. Genetics 2008; 178: 1947–1971. 10.1534/genetics.108.086983

[33]

Assmat E, Bazellires E, Pallesi-Pocachard E, Le Bivic A, Massey-Harroche D . Polarity complex proteins. Biochim Biophys Acta 2008; 1778: 614–630. 10.1016/j.bbamem.2007.08.029

[34]

MacDonald JM, Beach MG, Porpiglia E, Sheehan AE, Watts RJ, Freeman MR . The Drosophila cell corpse engulfment receptor Draper mediates glial clearance of severed axons. Neuron 2006; 50: 869–881. 10.1016/j.neuron.2006.04.028

[35]

Li W, Baker NE . Engulfment is required for cell competition. Cell 2007; 129: 1215–1225. 10.1016/j.cell.2007.03.054

[36]

Oldham S, Montagne J, Radimerski T, Thomas G, Hafen E . Genetic and biochemical characterization of dTOR, the Drosophila homolog of the target of rapamycin. Genes Dev 2000; 14: 2689–2694. 10.1101/gad.845700

[37]

Yaba A, Bianchi V, Borini A, Johnson J . A putative mitotic checkpoint dependent on mTOR function controls cell proliferation and survival in ovarian granulosa cells. Reprod Sci 2008; 15: 128–138. 10.1177/1933719107312037

[38]

Huang JH, Rajkovic A, Szafranski P, Ochsner S, Richards J, Goode S . Expression of Drosophila neoplastic tumor suppressor genes discs large, scribble, and lethal giant larvae in the mammalian ovary. Gene Expr Patterns 2003; 3: 3–11. 10.1016/s1567-133x(02)00096-0

[39]

Sarbassov DD, Ali SM, Sengupta S, Sheen JH, Hsu PP, Bagley AF et al. Prolonged rapamycin treatment inhibits mtorc2 assembly and akt/pkb. Mol Cell 2006; 22: 159–168. 10.1016/j.molcel.2006.03.029

[40]

Mirouse V, Swick LL, Kazgan N, St Johnston D, Brenman JE . LKB1 and AMPK maintain epithelial cell polarity under energetic stress. J Cell Biol 2007; 177: 387–392. 10.1083/jcb.200702053

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Published: May 07, 2010
Vol/Issue: 17(11)
Pages: 1717-1727
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Cite This Article

T C Thomson, J Johnson (2010). Inducible somatic oocyte destruction in response to rapamycin requires wild-type regulation of follicle cell epithelial polarity. Cell Death & Differentiation, 17(11), 1717-1727. https://doi.org/10.1038/cdd.2010.49

Inducible somatic oocyte destruction in response to rapamycin requires wild-type regulation of follicle cell epithelial polarity

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