1,197
Views
12
CrossRef citations to date
0
Altmetric
Review

Injury response checkpoint and developmental timing in insects

&
Pages 226-231 | Received 08 Dec 2014, Accepted 23 Mar 2015, Published online: 27 Apr 2015

References

  • Malá J, Sehnal F, Kumaran AK, Granger NA. Effects of starvation, chilling, and injury on endocrine gland function in Galleria mellonella. Arch. Insect Biochem. Physiol. 1987;4(2):113-128; http://dx.doi.org/10.1002/arch.940040205
  • Kunkel JG. Cockroach molting. II. The nature of regeneration-induced delay of molting hormone secretion. Biol. Bull. 1977;153(1):145-62; PMID:889943; http://dx.doi.org/10.2307/1540698
  • O’farrell A, Stock A. Regeneration and the Moulting Cycle in. Blattella Germanica L. III. Successive Regeneration of Both Metathoracic Legs. Aust. J. Biol. Sci. 1954;7(4):525-536; PMID:13229848
  • Pohley J. Experimentelle Beitrage zur Lenkung der Organentwicklung, des Hautungsrhytmus und der Metamorphose bei der Schabe Periplaneta americana L. Wilhelm Roux; Arch Entwicklungsmech Org. 1959;151:323-80.; http://dx.doi.org/10.1007/BF00577774
  • Stock A, O’Farrell AF. Regeneration and the moulting cycle in Blattella germanica L. II. Simultaneous regeneration of both metathoracic legs. Aust. J. Biol. Sci. 1954;7(3):302-7 PMID:13219037
  • Atli E, Unlü H. The effects of microwave frequency electromagnetic fields on the development of Drosophila melanogaster. Int. J. Radiat. Biol. 2006;82(6):435-41. PMID:16846978; http://dx.doi.org/10.1080/09553000600798849
  • Villee CA. Some effects of x-rays on development in Drosophila. J. Exp. Zool. 1946;101(2):261-280. ; http://dx.doi.org/10.1002/jez.1401010206
  • Bourgin RC, Krumins R, Quastler H. Radiation-Induced Delay of Pupation in Drosophila. Radiat. Res. 1956;5(6):657-673; PMID:13379619; http://dx.doi.org/10.2307/3570585
  • Madhavan K, Schneiderman H. Hormonal control of imaginal disc regeneration in galleria mellonella (lepidoptera). Biol. Bull. 1969;137(2):321-31; http://dx.doi.org/10.2307/1540104
  • Simpson P, Berreur P, Berreur-Bonnenfant J. The initiation of pupariation in Drosophila: dependence on growth of the imaginal discs. J. Embryol. Exp. Morphol. 1980;57:155-65; PMID:7430927
  • Stieper BC, Kupershtok M, Driscoll M V, Shingleton AW. Imaginal discs regulate developmental timing in Drosophila melanogaster. Dev. Biol. 2008;321(1):18-26. PMID:18632097.; http://dx.doi.org/10.1016/j.ydbio.2008.05.556
  • Poodry CA, Woods DF. Control of the developmental timer for Drosophila pupariation. Roux's Arch. Dev. Biol. 1990;199(4):219-227
  • Smith-Bolton RK, Worley MI, Kanda H, Hariharan IK. Regenerative growth in Drosophila imaginal discs is regulated by Wingless and Myc. Dev. Cell 2009;16(6):797-809; PMID:19531351
  • Halme A, Cheng M, Hariharan IK. Retinoids regulate a developmental checkpoint for tissue regeneration in Drosophila. Curr. Biol. 2010;20(5):458-63; PMID:20189388; http://dx.doi.org/10.1016/j.cub.2010.01.038
  • Hackney JF, Zolali-Meybodi O, Cherbas P. Tissue damage disrupts developmental progression and ecdysteroid biosynthesis in Drosophila. PLoS One 2012;7(11):e49105; PMID:23166607; http://dx.doi.org/10.1371/journal.pone.0049105
  • Pohley H. Regeneration and the moulting cycle in Ephestia kuhniella. In: Kiortis V, Trampusch H, eds. Regeneration in Animals. Amsterdam: North Holland Pub. Co.; 1965:324-30
  • Simpson P, Schneiderman HA. Isolation of temperature sensitive mutations blocking clone development in Drosophila melanogaster, and the effects of a temperature sensitive cell lethal mutation on pattern formation in imaginal discs. Wilhelm Roux's Arch. Dev. Biol. 1975;178(3):247-275
  • Brindley H. On the regeneration of the legs in the Blattidae. Zool Soc Proc 1897:907-16
  • O’Farrell AF, Stock A, Rae C, J.A. M. Regeneration and development in the cockroach B. germanica. Acta Soc Entomol Cech 1960;57:317-24
  • Villee CA. A Quantitative Study of Phenocopy Production with Monochromatic Ultraviolet Irradiation. Biol. Bull. 1947;92(1):1-9.; http://dx.doi.org/10.2307/1537964
  • Knobloch CA, Steel CGH. Interactions between limb regeneration and ecdysteroid titres in last larval instar Rhodnius prolixus (Hemiptera). J. Insect Physiol. 1988;34(6):507-514.; http://dx.doi.org/10.1016/0022-1910(88)90192-8
  • Garelli A, Gontijo AM, Miguela V, Caparros E, Dominguez M. Imaginal discs secrete insulin-like peptide 8 to mediate plasticity of growth and maturation. Science 2012;336(6081):579-82; PMID:22556250; http://dx.doi.org/10.1126/science.1216735
  • Johnson DG, Walker CL. Cyclins and cell cycle checkpoints. Annu. Rev. Pharmacol. Toxicol. 1999;39:295-312; PMID:10331086; http://dx.doi.org/10.1146/annurev.pharmtox.39.1.295
  • Davidowitz G, D’Amico LJ, Nijhout HF. Critical weight in the development of insect body size. Evol. Dev. 2003;5(2):188-97; PMID:12622736; http://dx.doi.org/10.1046/j.1525-142X.2003.03026.x
  • Nijhout HF, Williams CM. Control of Moulting and Metamorphosis in the Tobacco Hornworm, Manduca Sexta (L.): Cessation of Juvenile Hormone Secretion as a Trigger for Pupation. J. Exp. Biol. 1974;61(2):493-501
  • Mirth C, Truman JW, Riddiford LM. The role of the prothoracic gland in determining critical weight for metamorphosis in Drosophila melanogaster. Curr. Biol. 2005;15(20):1796-807; PMID:16182527; http://dx.doi.org/10.1016/j.cub.2005.09.017
  • Andres AJ, Cherbas P. Tissue-specific ecdysone responses: regulation of the Drosophila genes Eip28/29 and Eip40 during larval development. Development 1992;116(4):865-76; PMID:1295740
  • Worley MI, Setiawan L, Hariharan IK. Regeneration and transdetermination in Drosophila imaginal discs. Annu. Rev. Genet. 2012;46:289-310; PMID:22934642; http://dx.doi.org/10.1146/annurev-genet-110711-155637
  • Gateff E, Schneiderman HA. Developmental capacities of benign and malignant neoplasms of Drosophila. Wilhelm Roux Arch. für Entwicklungsmechanik der Org. 1974;176(1):23-65; http://dx.doi.org/10.1007/BF00577830
  • Stewart M, Murphy C, Fristrom JW. The recovery and preliminary characterization of X chromosome mutants affecting imaginal discs of Drosophila melanogaster. Dev. Biol. 1972;27(1):71-83; PMID:4621757; http://dx.doi.org/10.1016/0012-1606(72)90113-3
  • Bryant PJ. Regeneration and duplication following operations in situ on the imaginal discs of Drosophila melanogaster. Dev. Biol. 1971;26(4):637-651; PMID:5002603.; http://dx.doi.org/10.1016/0012-1606(71)90146-1
  • Woods DF, Bryant PJ. Molecular cloning of the lethal(1)discs large-1 oncogene of Drosophila. Dev. Biol. 1989;134(1):222-35; PMID:2471660; http://dx.doi.org/10.1016/0012-1606(89)90092-4
  • Martin P, Martin A, Shearn A. Studies of l(3)c43hs1 a polyphasic, temperature-sensitive mutant of Drosophila melanogaster with a variety of imaginal disc defects. Dev. Biol. 1977;55(2):213-32; PMID:402295; http://dx.doi.org/10.1016/0012-1606(77)90168-3
  • Bryant PJ, Schubiger G. Giant and duplicated imaginal discs in a new lethal mutant of Drosophila melanogaster. Dev. Biol. 1971;24(2):233-63; PMID:4994924; http://dx.doi.org/10.1016/0012-1606(71)90097-2
  • Rahn P. Untersuchungen zur Entwicklung von Ganz- und Teilimplantaten der Flügelimaginalscheibe vonEphestia kühniella Z. Wilhelm Roux. Arch. Entwickl. Mech. Org. 1972;170(1):48-82; http://dx.doi.org/10.1007/BF00575521
  • Dewes E. Regeneration in transplanted halves of male genital disks and its influence upon duration of development in Ephestia kühniella Z. Wilhelm Roux Arch. für Entwicklungsmechanik der Org. 1973;172(4):349-354; http://dx.doi.org/10.1007/BF00577885
  • Dewes E. Entwicklungsleistungen implantierter ganzer und halbierter männlicher Genitalimaginalscheiben von Ephestia kühniella Z. und Entwicklungsdauer der Wirtstiere. Wilhelm Roux's Arch. Dev. Biol. 1975;178(2):167-183
  • Sehnal F, Bryant PJ. Delayed pupariation in Drosophila imaginal disc overgrowth mutants is associated with reduced ecdysteroid titer. J. Insect Physiol. 1993;39(12):1051-1059; http://dx.doi.org/10.1016/0022-1910(93)90129-F
  • Gateff E. Malignant neoplasms of genetic origin in Drosophila melanogaster. Science 1978;200(4349):1448-59; PMID:96525; http://dx.doi.org/10.1126/science.96525
  • Kiss I, Molnár I. Metamorphic changes of wild type and mutant Drosophila tissues induced by 20-hydroxy ecdysone in vitro. J. Insect Physiol. 1980;26(6):391-401; http://dx.doi.org/10.1016/0022-1910(80)90010-4
  • Yamanaka N, Rewitz KF, O’Connor MB. Ecdysone Control of Developmental Transitions: Lessons from Drosophila Research. 2013 58:497-516; PMID:23072462
  • Riddiford LM. Hormone receptors and the regulation of insect metamorphosis. Receptor 1993;3(3):203-9; PMID:8167571
  • Buszczak M, Freeman MR, Carlson JR, Bender M, Cooley L, Segraves WA. Ecdysone response genes govern egg chamber development during mid-oogenesis in Drosophila. Development 1999;126(20):4581-9; PMID:10498692
  • Carney GE, Bender M. The Drosophila ecdysone receptor (EcR) gene is required maternally for normal oogenesis. Genetics 2000;154(3):1203-11; PMID:10757764
  • Chavoshi TM, Moussian B, Uv A. Tissue-autonomous EcR functions are required for concurrent organ morphogenesis in the Drosophila embryo. Mech. Dev. 2010;127(5-6):308-19; PMID:20093179; http://dx.doi.org/10.1016/j.mod.2010.01.003
  • Fristrom JW, Logan WR, Murphy C. The synthetic and minimal culture requirements for evagination of imaginal discs of Drosophila melanogaster in vitro. Dev. Biol. 1973;33(2):441-456; PMID:4207978; http://dx.doi.org/10.1016/0012-1606(73)90149-8
  • Martin P, Shearn A. Development of Drosophila imaginal discs in vitro: Effects of ecdysone concentration and insulin. J. Exp. Zool. 1980;211(3):291-301.; http://dx.doi.org/10.1002/jez.1402110306
  • Postlethwait JH, Schneiderman HA. Induction of metamorphosis by ecdysone analogues. Drosophila imaginal discs cultured in vivo. Biol. Bull. 1970;138(1):47-55; PMID:5437915; http://dx.doi.org/10.2307/1540290
  • Guillermet C, Mandaron P. In vitro imaginal disc development and moulting hormone. J Embryol Exp Morphol 1980;57(1):107-118; PMID:6776221
  • Mandaron P, Guillerment C, Sengel P. In Vitro Development of Drosophila Imaginal Discs: Hormonal Control and Mechanism of Evagination. Integr. Comp. Biol. 1977;17(3):661-670; http://dx.doi.org/10.1093/icb/17.3.661
  • Ashburner M. Sequential gene activation by ecdysone in polytene chromosomes of Drosophila melanogaster. Dev. Biol. 1974;39(1):141-157; PMID:4209831.; http://dx.doi.org/10.1016/S0012-1606(74)80016-3
  • Ashburner M, Chihara C, Meltzer P, Richards G. Temporal control of puffing activity in polytene chromosomes. Cold Spring Harb. Symp. Quant. Biol. 1974;38:655-62; http://dx.doi.org/10.1101/SQB.1974.038.01.070
  • Boyd M, Ashburner M. The hormonal control of salivary gland secretion in Drosophila melanogaster: Studies in vitro. J. Insect Physiol. 1977;23(4):517-523; http://dx.doi.org/10.1016/0022-1910(77)90263-3
  • Kraminsky GP, Clark WC, Estelle MA, Gietz RD, Sage BA, O'Connor JD, Hodgetts RB. Induction of translatable mRNA for dopa decarboxylase in Drosophila: an early response to ecdysterone. Proc. Natl. Acad. Sci. U. S. A. 1980;77(7):4175-9; PMID:6776524; http://dx.doi.org/10.1073/pnas.77.7.4175
  • Schwartz LM, Truman JW. Hormonal control of muscle atrophy and degeneration in the moth Antheraea polyphemus. J. Exp. Biol. 1984;111:13-30; PMID:6491588
  • Ninov N, Manjón C, Martín-Blanco E. Dynamic control of cell cycle and growth coupling by ecdysone, EGFR, and PI3K signaling in Drosophila histoblasts. PLoS Biol. 2009;7(4):e1000079; PMID:19355788; http://dx.doi.org/10.1371/journal.pbio.1000079
  • Smith WA, Gilbert LI, Bollenbacher WE. Calcium-cyclic AMP interactions in prothoracicotropic hormone stimulation of ecdysone synthesis. Mol. Cell. Endocrinol. 1985;39(1):71-8; PMID:2982678; http://dx.doi.org/10.1016/0303-7207(85)90093-0
  • Smith WA, Combest WL, Gilbert LI. Involvement of cyclic AMP-dependent protein kinase in prothoracicotropic hormone-stimulated ecdysone synthesis. Mol. Cell. Endocrinol. 1986;47(1-2):25-33; PMID:3017787; http://dx.doi.org/10.1016/0303-7207(86)90012-2
  • Gilbert LI, Combest WL, Smith WA, Meller VH, Rountree DB. Neuropeptides, second messengers and insect molting. Bioessays 1988;8(5):153-7; PMID:3044357; http://dx.doi.org/10.1002/bies.950080506
  • McBrayer Z, Ono H, Shimell M, Parvy JP, Beckstead RB, Warren JT, Thummel CS, Dauphin-Villemant C, Gilbert LI, O'Connor MB. Prothoracicotropic hormone regulates developmental timing and body size in Drosophila. Dev. Cell 2007;13(6):857-71; PMID:18061567
  • Zdarek J, Fraenkel G. Neurosecretory control of ecdysone release during puparium formation of flies. Gen. Comp. Endocrinol. 1971;17(3):483-489; PMID:5128300; http://dx.doi.org/10.1016/0016-6480(71)90183-3
  • Roberts B, Gilbert LI, Bollenbacher WE. In vitro activity of dipteran ring glands and activation by the prothoracicotropic hormone. Gen. Comp. Endocrinol. 1984;54(3):469-77; PMID:6735164; http://dx.doi.org/10.1016/0016-6480(84)90164-3
  • Harvie PD, Filippova M, Bryant PJ. Genes expressed in the ring gland, the major endocrine organ of Drosophila melanogaster. Genetics 1998;149(1):217-31; PMID:9584098
  • Neubueser D, Warren JT, Gilbert LI, Cohen SM. molting defective is required for ecdysone biosynthesis. Dev. Biol. 2005;280(2):362-72; PMID:15882578; http://dx.doi.org/10.1016/j.ydbio.2005.01.023
  • Wismar J, Habtemichael N, Warren JT, Dai JD, Gilbert LI, Gateff E. The mutation without children(rgl) causes ecdysteroid deficiency in third-instar larvae of Drosophila melanogaster. Dev. Biol. 2000;226(1):1-17; PMID:10993670; http://dx.doi.org/10.1006/dbio.2000.9811
  • Takeuchi H, Chen J, O’Reilly D, Rees H, Turner P. Regulation of ecdysteroid signalling: molecular cloning, characterization and expression of 3-dehydroecdysone 3α-reductase, a novel eukaryotic member of the short-chain dehydrogenases/reductases superfamily from the cotton leafworm, Spodoptera littoralis. 2000;349(Pt 1):239-245; PMID:10861234
  • Hadorn E. An Accelerating Effect of Normal “Ring-Glands” on Puparium-Formation in Lethal Larvae of Drosophila Melanogaster. Proc. Natl. Acad. Sci. U. S. A. 1937;23(9):478-84; PMID:16577798; http://dx.doi.org/10.1073/pnas.23.9.478
  • Waddington CH, Robertson E. Determination, activation and actinomycin D insensitivity in the optic imaginal disk of Drosophila. Nature 1969;221(5184):933-5; PMID:5765504; http://dx.doi.org/10.1038/221933a0
  • Colombani J, Andersen DS, Léopold P. Secreted peptide Dilp8 coordinates Drosophila tissue growth with developmental timing. Science 2012;336(6081):582-5; PMID:22556251; http://dx.doi.org/10.1126/science.1216689
  • Shingleton AW, Das J, Vinicius L, Stern DL. The temporal requirements for insulin signaling during development in Drosophila. PLoS Biol. 2005;3(9):e289; PMID:16086608; http://dx.doi.org/10.1371/journal.pbio.0030289
  • Böhni R, Riesgo-Escovar J, Oldham S, Brogiolo W, Stocker H, Andruss BF, Beckingham K, Hafen E. Autonomous control of cell and organ size by CHICO, a Drosophila homolog of vertebrate IRS1-4. Cell 1999;97(7):865-75; PMID:10399915; http://dx.doi.org/10.1016/S0092-8674(00)80799-0
  • Kramer JM, Davidge JT, Lockyer JM, Staveley BE. Expression of Drosophila FOXO regulates growth and can phenocopy starvation. BMC Dev. Biol. 2003;3:5; PMID:12844367.; http://dx.doi.org/10.1186/1471-213X-3-5
  • Shearn A, Rice T, Garen A, Gehring W. Imaginal disc abnormalities in lethal mutants of Drosophila. Proc. Natl. Acad. Sci. U. S. A. 1971;68(10):2594-8; PMID:5002822; http://dx.doi.org/10.1073/pnas.68.10.2594
  • Szabad J, Bryant PJ. The mode of action of “discless” mutations in Drosophila melanogaster. Dev. Biol. 1982;93(1):240-256; PMID:6813163.; http://dx.doi.org/10.1016/0012-1606(82)90256-1
  • Mensch J, Lavagnino N, Carreira VP, Massaldi A, Hasson E, Fanara JJ. Identifying candidate genes affecting developmental time in Drosophila melanogaster: pervasive pleiotropy and gene–by-environment interaction. BMC Dev. Biol. 2008;8(1):78; PMID:18687152; http://dx.doi.org/10.1186/1471-213X-8-78
  • Johnston LA, Prober DA, Edgar BA, Eisenman RN, Gallant P. Drosophila myc regulates cellular growth during development. Cell 1999;98(6):779-90; PMID:10499795; http://dx.doi.org/10.1016/S0092-8674(00)81512-3
  • Jacobs HW, Knoblich JA, Lehner CF. Drosophila Cyclin B3 is required for female fertility and is dispensable for mitosis like Cyclin B. Genes Dev. 1998;12(23):3741-51; PMID:9851980; http://dx.doi.org/10.1101/gad.12.23.3741
  • Manak JR, Mitiku N, Lipsick JS. Mutation of the Drosophila homologue of the Myb protooncogene causes genomic instability. Proc. Natl. Acad. Sci. U. S. A. 2002;99(11):7438-43; PMID:12032301; http://dx.doi.org/10.1073/pnas.122231599
  • Stevens ME, Bryant PJ. Temperature-dependent expression of the apterous phenotype in Drosophila melanogaster. Genetics 1986;112(2):217-28; PMID:3079719
  • Shi W, Stampas A, Zapata C, Baker NE. The pineapple eye gene is required for survival of Drosophila imaginal disc cells. Genetics 2003;165(4):1869-79; PMID:14704172
  • Dolecek R, Dvorácek C, Jezek M, Kubis M, Sajnar J, Závada M. Very low serum testosterone levels and severe impairment of spermatogenesis in burned male patients. Correlations with basal levels and levels of FSH, LH and PRL after LHRH + TRH. Endocrinol. Exp. 1983;17(1):33-45; PMID:6409583
  • Pozo J, Argente J. Delayed puberty in chronic illness. Best Pract. Res. Clin. Endocrinol. Metab. 2002;16(1):73-90; PMID:11987900; http://dx.doi.org/10.1053/beem.2002.0182
  • Simon D. Puberty in chronically diseased patients. Horm. Res. 2002;57 Suppl 2:53-6; PMID:12065928; http://dx.doi.org/10.1159/000058102
  • Mavoungou D, Poaty-Mavoungou V, Ongali B, Akoume MY, Maka G, Mavoungou E. Hypothalamic-pituitary gonadal axis and immune response imbalance during chronic filarial infections. Trop. Med. Int. Health 2005;10(11):1180-6; PMID:16262744; http://dx.doi.org/10.1111/j.1365-3156.2005.01499.x
  • Dolecek R. Endocrine changes after burn trauma–a review. Keio J. Med. 1989;38(3):262-76; PMID:2511373; http://dx.doi.org/10.2302/kjm.38.262
  • Emanuele NV, LaPaglia N, Kovacs EJ, Gamelli RL, Emanuele MA. Profound effects of burn and ethanol on proinflammatory cytokines of the reproductive axis in the male mouse. J. Burn Care Res. 29(3):531-40; PMID:18388566; http://dx.doi.org/10.1097/BCR.0b013e3181711273
  • Rewitz KF, Rybczynski R, Warren JT, Gilbert LI. The Halloween genes code for cytochrome P450 enzymes mediating synthesis of the insect moulting hormone. Biochem. Soc. Trans. 2006;34(Pt 6):1256-60; PMID:17073797

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.