Abstract
Extensive programmed cell death occurs in the female germline of many species ranging from C. elegans to humans. One purpose for germline apoptosis is to remove defective cells unable to develop into fertile eggs. In addition, recent work suggests that the death of specific germline cells may also play a vital role by providing essential nutrients to the surviving oocytes. In Drosophila, the genetic control of germline apoptosis and the proteins that carry out the death sentences are beginning to emerge from studies of female sterile mutations. These studies suggest that the morphological changes that occur during the late stages of Drosophila oogenesis may be initiated and driven by a modified form of programmed cell death. Cell Death and Differentiation (2000) 7, 1071–1074
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References
De Pol A, Vaccina F, Forabosco A, Cavazzuti E and Marzona L . 1997 Apoptosis of germ cells during human prenatal oogenesis. Hum. Reprod. 12: 2235–2241
De Pol A, Marzona L, Vaccina F, Negro R, Sena P and Forabosco A . 1998 Apoptosis in different stages of human oogenesis. Anticancer Res. 18: 3457–3461
Cavaliere V, Taddei C and Gargiulo G . 1998 Apoptosis of nurse cells at the late stages of oogenesis of Drosophila melanogaster. Dev. Genes Evol. 208: 106–112
Foley K and Cooley L . 1998 Apoptosis in late stage Drosophila nurse cells does not require genes within the H99 deficiency. Development 125: 1075–1082
Gumienny TL, Lambie E, Hartwieg E, Horvitz HR and Hengartner MO . 1999 Genetic control of programmed cell death in the Caenorhabditis elegans hermaphrodite germline. Development 126: 1011–1022
Baker TG and Sum W . 1976 Development of the ovary and oogenesis. Clin. Obstet. Gynaecol. 3: 3–26
Spradling AC . 1993 Developmental Genetics of Oogenesis. In: Bate M, Martinez Arias A (eds). The Development of Drosophila menalogaster. Cold Spring Harbor Laboratory Press: Cold Spring Harbor pp. 1–70
Robinson DN and Cooley L . 1996 Stable intercellular bridges in development: the cytoskeleton lining the tunnel. Trends Cell Biol. 6: 474–479
Giorgi F and Deri P . 1976 Cell death in ovarian chambers of Drosophila melanogaster. J. Embryol. Exp. Morph. 35: 521–533
Thummel CS . 1996 Flies on steroids–Drosophila metamorphosis and the mechanisms of steroid hormone action. Trends Genet. 12: 306–310
Buszczak M, Freeman MR, Carlson JR, Bender M, Cooley L and Segraves WA . 1999 Ecdysone response genes govern egg chamber development during mid-oogenesis in Drosophila. Development 126: 4581–4589
Mahajan-Miklos S and Cooley L . 1994 Intercellular cytoplasm transport during Drosophila oogenesis. Dev. Biol. 165: 336–351
Guild GM, Connelly PS, Shaw MK and Tilney LG . 1997 Actin filament cables in Drosophila nurse cells are composed of modules that slide passively past one another during dumping. J. Cell Biol. 138: 783–797
Matova N, Mahajaran-Miklos S, Mooseker MS and Cooley L . 1999 Drosophila quail, a villin-related protein, bundles actin filaments in apoptotic nurse cells. Development 126: 5645–5657
Lam M, Dubyak G and Distelhorst CW . 1993 Effect of glucocorticosteroid treatment on intracellular calcium homeostasis in mouse lymphoma cells. Mol. Endocrinol. 7: 686–693
Lam M, Dubyak G, Chen L, Nunez G, Miesfeld RL and Distelhorst CW . 1994 Evidence that BCL-2 represses apoptosis by regulating endoplasmic reticulum-associated Ca2+ fluxes. Proc. Natl. Acad. Sci. USA 91: 6569–6573
Chen P, Rodriguez A, Erskine R, Thach T and Abrams JM . 1998 Dredd, a novel effector of the apoptosis activators reaper, grim, and hid in Drosophila. Dev. Biol. 201: 202–216
Dorstyn L, Colussi PA, Quinn LM, Richardson H and Kumar S . 1999 DRONC, an ecdysone-inducible Drosophila caspase. Proc. Natl. Acad. Sci. USA 96: 4307–4312
Varkey J, Chen P, Jemmerson R and Abrams JM . 1999 Altered cytochrome c display precedes apoptotic cell death in Drosophila. J. Cell Biol. 144: 701–710
Dorstyn L, Read SH, Quinn LM, Richardson H and Kumar S . 1999 DECAY, a novel Drosophila caspase related to mammalian caspase-3 and caspase-7. J. Biol. Chem. 274: 30778–30783
Colussi PA, Quinn LM, Huang DC, Coombe M, Read SH, Richardson H and Kumar S . 2000 Debcl, a proapoptotic Bcl-2 homologue, is a component of the Drosophila melanogaster cell death machinery. J. Cell Biol. 148: 703–714
McCall K and Steller H . 1998 Requirement for DCP-1 caspase during Drosophila oogenesis. Science 279: 230–234
Cooley L, Verheyen E and Ayers K . 1992 chickadee encodes a profilin required for intercellular cytoplasm transport during Drosophila oogenesis. Cell 69: 173–184
Cant K, Knowles BA, Mooseker MS and Cooley L . 1994 Drosophila singed, a fascin homolog, is required for actin bundle formation during oogenesis and bristle extension. J. Cell Biol. 125: 369–380
Mahajan-Miklos S and Cooley L . 1994 The villin-like protein encoded by the Drosophila quail gene is required for actin bundle assembly during oogenesis. Cell 78: 291–301
Wheatley S, Kulkarni S and Karess R . 1995 Drosophila nonmuscle myosin II is required for rapid cytoplasmic transport during oogenesis and for axial nuclear migration in early embryos. Development 121: 1937–1946
Edwards KA and Kiehart DP . 1996 Drosophila nonmuscle myosin II has multiple roles in imaginal discs and egg chamber morphogenesis. Development 122: 1499–1511
White K, Grether ME, Abrams JM, Young L, Farrell K and Steller H . 1994 Genetic control of programmed cell death in Drosophila. Science 264: 677–683
Grether ME, Abrams JM, Agapite J, White K and Steller H . 1995 The head involution defective gene of Drosophila melanogaster functions in programmed cell death. Genes Dev. 9: 1694–1708
Chen P, Nordstrom W, Gish B and Abrams JM . 1996 grim, a novel cell death gene in Drosophila. Genes Dev. 10: 1773–1782
Jiang C, Baehrecke EH and Thummel CS . 1997 Steroid regulated programmed cell death during Drosophila metamorphosis. Development 124: 4673–4683
Jiang C, Lamblin AF, Steller H and Thummel CS . 2000 A steroid-triggered transcriptional hierarchy controls salivary gland cell death during Drosophila metamorphosis. Mol. Cell 5: 445–455
Soller M, Bownes M and Kubli E . 1999 Control of oocyte maturation in sexually mature Drosophila females. Dev. Biol. 208: 337–351
Twombly V, Blackman RK, Jin H, Graff JM, Padgett RW and Gelbart WM . 1996 The TGF-beta signaling pathway is essential for Drosophila oogenesis. Development 122: 1555–1565
Acknowledgements
We would like to thank M Shaw, L Tilney, K Foley, A Rodriguez, J Varkey and J Abrams for images used in this review. This work was supported by a grant from the NIH to L Cooley (GM43301).
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Buszczak, M., Cooley, L. Eggs to die for: cell death during Drosophila oogenesis. Cell Death Differ 7, 1071–1074 (2000). https://doi.org/10.1038/sj.cdd.4400755
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DOI: https://doi.org/10.1038/sj.cdd.4400755
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