The DOI matches its Crossref record; 83 of the 83 references it cites were found in a registry or an index.
Steroid regulated programmed cell death during Drosophila metamorphosis
Abstract
During insect metamorphosis, pulses of the steroid hormone 20-hydroxyecdysone (ecdysone) direct the destruction of obsolete larval tissues and their replacement by tissues and structures that form the adult fly. We show here that larval midgut and salivary gland histolysis are stage-specific steroid-triggered programmed cell death responses. Dying larval midgut and salivary gland cell nuclei become permeable to the vital dye acridine orange and their DNA undergoes fragmentation, indicative of apoptosis. Furthermore, the histolysis of these tissues can be inhibited by ectopic expression of the baculovirus antiapoptotic protein p35, implicating a role for caspases in the death response. Coordinate stage-specific induction of the Drosophila death genes reaper (rpr) and head involution defective (hid) immediately precedes the destruction of the larval midgut and salivary gland. In addition, the diap2 anti-cell death gene is repressed in larval salivary glands as rpr and hid are induced, suggesting that the death of this tissue is under both positive and negative regulation. Finally, diap2 is repressed by ecdysone in cultured salivary glands under the same conditions that induce rpr expression and trigger programmed cell death. These studies indicate that ecdysone directs the death of larval tissues via the precise stage- and tissue-specific regulation of key death effector genes.
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Cites
Apoptosis: A Basic Biological Phenomenon with Wideranging Implications in Tissue Kinetics
Kerr, J. F. R., Wyllie, A. H., & Currie, A. R. (1972) · British Journal of Cancer · doi:10.1038/bjc.1972.33 · Cited by 15,725
Targeted gene expression as a means of altering cell fates and generating dominant phenotypes
Brand, A. H., & Perrimon, N. (1993) · Development · doi:10.1242/dev.118.2.401 · Cited by 9,612
Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation.
Gavrieli, Y., Sherman, Y., & Ben-Sasson, S. A. (1992) · The Journal of cell biology · doi:10.1083/jcb.119.3.493 · Cited by 9,444
Glucocorticoid-induced thymocyte apoptosis is associated with endogenous endonuclease activation
Wyllie, A. H. (1980) · Nature · doi:10.1038/284555a0 · Cited by 4,504
The Genetics and Biology of Drosophila
(1978) · Food and Cosmetics Toxicology · doi:10.1016/s0015-6264(78)80200-4 · Cited by 3,755
The development of Drosophila melanogaster
Ingham, P. (1994) · Trends in Genetics · doi:10.1016/0168-9525(90)90017-z · Cited by 3,149
Programmed Cell Death in Animal Development
Jacobson, M. D., Weil, M., & Raff, M. C. (1997) · Cell · doi:10.1016/s0092-8674(00)81873-5 · Cited by 2,698
Social controls on cell survival and cell death
Raff, M. C. (1992) · Nature · doi:10.1038/356397a0 · Cited by 2,604
Mechanisms and Genes of Cellular Suicide
Steller, H. (1995) · Science · doi:10.1126/science.7878463 · Cited by 2,479
The embryonic development of Drosophila melanogaster
(1938) · Protoplasma · doi:10.1007/bf01613769 · Cited by 2,142
Cited by
MicroRNA targets in Drosophila
Enright, A. J., John, B., Gaul, U., Tuschl, T., Sander, C., & Marks, D. S. (2003) · Genome Biology · doi:10.1186/gb-2003-5-1-r1 · Cited by 3,597
Autophagy-dependent cell death
Denton, D., & Kumar, S. (2019) · Cell Death & Differentiation · doi:10.1038/s41418-018-0252-y · Cited by 777
Doherty, J., & Baehrecke, E. H. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0201-5 · Cited by 624
Self-citationGeorgel, P., Naitza, S., Kappler, C., Ferrandon, D., Zachary, D., Swimmer, C., Kopczynski, C., Duyk, G., Reichhart, J.-M., & Hoffmann, J. A. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00059-4 · Cited by 448
Cell death by autophagy: facts and apparent artefacts
Denton, D., Nicolson, S., & Kumar, S. (2012) · Cell Death & Differentiation · doi:10.1038/cdd.2011.146 · Cited by 381
Die another way – non-apoptotic mechanisms of cell death
Tait, S. W. G., Ichim, G., & Green, D. R. (2014) · Journal of Cell Science · doi:10.1242/jcs.093575 · Cited by 366
Drosophila Ecdysone Receptor Mutations Reveal Functional Differences among Receptor Isoforms
Bender, M., Imam, F. B., Talbot, W. S., Ganetzky, B., & Hogness, D. S. (1997) · Cell · doi:10.1016/s0092-8674(00)80466-3 · Cited by 280
Filonova, L. H., Bozhkov, P. V., Brukhin, V. B., Daniel, G., Zhivotovsky, B., & Arnold, S. V. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.24.4399 · Cited by 257
Genome-Wide Analyses of Steroid- and Radiation-Triggered Programmed Cell Death in Drosophila
Lee, C.-Y., Clough, E. A., Yellon, P., Teslovich, T. M., Stephan, D. A., & Baehrecke, E. H. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00085-x · Cited by 215
Self-citationA SAGE Approach to Discovery of Genes Involved in Autophagic Cell Death
Gorski, S. M., Chittaranjan, S., Pleasance, E. D., Freeman, J. D., Anderson, C. L., Varhol, R. J., Coughlin, S. M., Zuyderduyn, S. D., Jones, S. J. M., & Marra, M. A. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00082-4 · Cited by 213
The role of larval fat cells in adult Drosophila melanogaster
Aguila, J. R., Suszko, J., Gibbs, A. G., & Hoshizaki, D. K. (2007) · Journal of Experimental Biology · doi:10.1242/jeb.001586 · Cited by 212
A role for juvenile hormone in the prepupal development of Drosophila melanogaster
Riddiford, L. M., Truman, J. W., Mirth, C. K., & Shen, Y.-C. (2010) · Development · doi:10.1242/dev.037218 · Cited by 194
Uba1 functions in Atg7- and Atg3-independent autophagy
Chang, T.-K., Shravage, B. V., Hayes, S. D., Powers, C. M., Simin, R. T., Wade Harper, J., & Baehrecke, E. H. (2013) · Nature Cell Biology · doi:10.1038/ncb2804 · Cited by 187
Self-citationGenetic Control of Programmed Cell Death During Animal Development
Conradt, B. (2009) · Annual Review of Genetics · doi:10.1146/annurev.genet.42.110807.091533 · Cited by 173
Steroid signaling in plants and insects—common themes, different pathways
Thummel, C. S., & Chory, J. (2002) · Genes & Development · doi:10.1101/gad.1042102 · Cited by 161
Self-citationPecasse, F., Beck, Y., Ruiz, C., & Richards, G. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9687 · Cited by 129
Sequence and functional properties of Ets genes in the model organism Drosophila
Hsu, T., & Schulz, R. A. (2000) · Oncogene · doi:10.1038/sj.onc.1204033 · Cited by 85
Relationship between growth arrest and autophagy in midgut programmed cell death in Drosophila
Denton, D., Chang, T.-K., Nicolson, S., Shravage, B., Simin, R., Baehrecke, E. H., & Kumar, S. (2012) · Cell Death & Differentiation · doi:10.1038/cdd.2012.43 · Cited by 81
Self-citationDevelopmentally programmed cell death in Drosophila
Denton, D., Aung-Htut, M. T., & Kumar, S. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.06.014 · Cited by 75
Mills, K., Daish, T., Harvey, K. F., Pfleger, C. M., Hariharan, I. K., & Kumar, S. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200512126 · Cited by 70
Non-apoptotic cell death in animal development
Kutscher, L. M., & Shaham, S. (2017) · Cell Death & Differentiation · doi:10.1038/cdd.2017.20 · Cited by 67
miR-14 Regulates Autophagy during Developmental Cell Death by Targeting ip3-kinase 2
Nelson, C., Ambros, V., & Baehrecke, E. H. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.09.011 · Cited by 61
Self-citationTruman, J. W., & Riddiford, L. M. (2023) · GENETICS · doi:10.1093/genetics/iyac184 · Cited by 60
UTX coordinates steroid hormone-mediated autophagy and cell death
Denton, D., Aung-Htut, M. T., Lorensuhewa, N., Nicolson, S., Zhu, W., Mills, K., Cakouros, D., Bergmann, A., & Kumar, S. (2013) · Nature Communications · doi:10.1038/ncomms3916 · Cited by 58
Lippai, M., Csikós, G., Maróy, P., Lukácsovich, T., Juhász, G., & Sass, M. (2008) · Autophagy · doi:10.4161/auto.5719 · Cited by 56
Lam, G., Nam, H.-J., Velentzas, P. D., Baehrecke, E. H., & Thummel, C. S. (2022) · Developmental Biology · doi:10.1016/j.ydbio.2021.10.001 · Cited by 38
Self-citationShen, J. L., Fortier, T. M., Zhao, Y. G., Wang, R., Burmeister, M., & Baehrecke, E. H. (2021) · Current Biology · doi:10.1016/j.cub.2021.04.062 · Cited by 36
Self-citationThe Proton-Coupled Monocarboxylate Transporter Hermes Is Necessary for Autophagy during Cell Death
Velentzas, P. D., Zhang, L., Das, G., Chang, T.-K., Nelson, C., Kobertz, W. R., & Baehrecke, E. H. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.09.015 · Cited by 31
Self-citationLiu, C., Wu, M., Zheng, Z., Fan, S., Tan, J., Jiao, Y., Palli, S. R., & Zhu, G. (2025) · Pest Management Science · doi:10.1002/ps.8592 · Cited by 9
Metadata
- Authors
- Jiang, C., Baehrecke, E. H., & Thummel, C. S.
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 1997-11-15
- Volume
- 124
- Issue
- 22
- Pages
- 4673-4683
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W2171784464
- Cited by
- 391
- References
- 83
- FWCI
- 5.63
- Type
- journal article
- Language
- en
- Open access
- closed
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