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The induction of triploidy in Oreochromis aureus by heat shock

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Summary

Triploid fish were obtained using heat-shock treatment. The optimal conditions for the heat shock (39.5±0.2°C for 3.5–4 min) as well as the exact zygote age (3 min) at which this heat shock was applied were studied. Results showed that this treatment gives rise to 100% of triploid fish with a satisfactory survival rate of 61% beyond the yolk sac resorption. The genital papillae of this triploid fish were underdeveloped in comparison to normal diploid fish. However, no morphological or growth-rate differences between diploid and triploid fish could be observed up to the age of 6 months. Triploidy was assessed by the karyotyping of embryo cells or adult PHA-stimulated lymphocytes, or by erythrocyte measurements. The occurrence of a heat-shock sensitive event at the zygotic age of 6 min is discussed.

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References

  • Allen SK, Stanley JG (1979) Polyploid mosaics induced by cytochalasin B in landlocked Atlantic salmon Salmo-salar. Trans Am Fish Soc 18:462–466

    Google Scholar 

  • Ashburner M, Bonner JJ (1979) The induction of gene activity in Drosophila by heat shock. Cell 17:241–254

    Google Scholar 

  • Avtalion RR (1982) Genetic markers in Sarotherodom and their use for sex and species identification. In: Pullin RSV, Lowe-McConnell RH (eds) The biology and culture of tilapia. ICLARM, pp 269–277

  • Beck ML, Biggers CJ (1983) Ploidy of hybrids between Grass carp and Bighead carp determined by morphological analysis. Trans Am Fish Soc 112:808–811

    Google Scholar 

  • Beck ML, Briggers CJ (1983) Erythrocyte measurements of diploid and triploid Ctenopharyngodon idella x Hypophthalmichthys nobilis hybrids. J Fish Biol 22:497–502

    Google Scholar 

  • Benfey TJ, Sutterlin AM (1984) The haematology of triploid landlocked Atlantic salmon (Salmo salar L). J Fish Biol 24:333–338

    Google Scholar 

  • Benfey TJ, Sutterlin AM (1984) Triploidy induced by heat shock and hydrostatic pressure in landlocked Atlantic salmon (Salmo salar L). Aquaculture 36:359–367

    Google Scholar 

  • Benfey TJ, Sutterlin AM, Thompson RT (1984) Use of erythrocyte measurements to identify triploid salmonids. Can J Fish Aquat Sci 41:980–984

    Google Scholar 

  • Benfey TJ, Sutterlin A (1984) Growth and gonadal development in triploid landlocked Atlantic salmon (Salmo salar). Can J Fish Aquat Sci 41:1387–1392

    Google Scholar 

  • Bensaude O, Babinet C, Marange M, Jacob F (1983) Heat shock proteins, first major product of zygotic gene activity in mouse embryo. Nature 305:331–333

    Google Scholar 

  • Cherfas NB (1979) Gynogenesis in fish. In: Kirpichnikov VS (ed) Genetic bases of fish selection. Springer, Berlin Heidelberg New York, pp 255–273

    Google Scholar 

  • Chourrout D (1980) Termal induction of diploid gynogenesis and triploidy in the rainbow trout (Salmo gairdneri R.). Reprod Nutr Dev 20:726–733

    Google Scholar 

  • Chourrout D, Quillet E (1982) Induced gynogenesis in the Rainbow trout: sex and survival of progenies, production of all triploid population. Theor Appl Genet 63:201–205

    Google Scholar 

  • Chourrout D, Itskovich J (1983) Three manipulations permitted by artificial insemination in Tilapia: induced diploid gynogenesis, production of all triploid population and intergeneric hybridization. In: Int Symp Tilapia in aquaculture. Nazareth, Israel, pp 246–255

  • Chourrout D (1984) Pressure induced retention of second polar body and suppression of first cleavage in Rainbow trout: production of all triploid and heterozygous and homozygous diploid gynogenetics. Aquaculture 36:111–126

    Google Scholar 

  • Edwards RG (1958a) Colchicin induced heteroploidy in the mouse. 1. The induction of triploidy by treatment of the gametes. J Exp Zool 137:317–348

    Google Scholar 

  • Edwards RG, (1958b) Colchicin induced heteroploidy in the mouse. 2. The induction of tetraploidy and other types of heteroploidy. J Exp Zool 137:349–362

    Google Scholar 

  • Galman OR, Avtalion RR (unpublished) Further studies on the embryonic development of O. aureus (Cichlidae teleostei) using scanning electron and light microscopies

  • Gervai J, Peter S, Nagy A, Horvath L, Coanyi V (1980) Induced triploidy in carp, Cyprinus carpio L. J Fish Biol 17:667–671

    Google Scholar 

  • Koiller M, Avtalion RR (1985) A laboratory scale recycling water unit for Tilapia breeding. Aquacult Engin 4:235–246

    Google Scholar 

  • Mires D (1982) A study of the problems of the mass production of hybrid tilapia fry. In: Pullin RSV, Lowe-McConnell RH (eds) The biology and culture of tilapias. ICLARM, pp 317–329

  • Nagy A, Rajki K, Horvath L, Csanyi V (1978) Investigation on carp. (Cyprinus carpio L.) gynogenesis. J Fish Biol 13:215–224

    Google Scholar 

  • Nevins JR (1982) Induction of the synthesis of a 70,000 dalton mammalian heat shock protein by the adenovirus E1A gene product. Cell 29:913–919

    Google Scholar 

  • Purdom CE (1972) Induced polyploidy in plaice (Pleuronectes platessd) and its hybrid with the flounder (Platichythys flesus). Heredity 29:11–24

    Google Scholar 

  • Refstie T, Vassvik V, Gjedrem T (1977) Induction of polyploidy in salmonids by Cytochalasin B. Aquaculture 10:65–74

    Google Scholar 

  • Refstie T (1983): Induction of diploid gynogenesis in Atlantic salmon and Rainbow trout using irradiated sperm and heat shock. Can J Zool 61:2411–2416

    Google Scholar 

  • Reinschmidt DC, Simon SJ, Valpe EP, Tompkins R (1979) Production of tetraploid and homozygous diploid amphibians by supression of first cleavage. J Exp Zool 210:137–143

    Google Scholar 

  • Rothbard S, Hulsta G (1980): Closed system incubator for cichlid eggs. Prog Fish Cult 42:203–204

    Google Scholar 

  • Snow, MHL (1973) Tetraploid mouse embryos production by cytochalasin B. during cleavage. Nature 244:513–515

    Google Scholar 

  • Stanley JG, Hidu H, Allen SK (1984) Growth of american oysters increased by polyploidy induced by blocking meiosis I. but not meiosis II. Aquaculture 37:147–155

    Google Scholar 

  • Swarup H (1959a): Production of triploidy in Gasterosteus aculeatus (L.). J Genet 56:129–142

    Google Scholar 

  • Swarup H (1959b) Effects of triploidy on the body size, general organization and cellular structure in Gasterosteus aculeatus (L.). J Genet 56:143–155

    Google Scholar 

  • Thorgaard GH, Gall GAE (1979) Adult triploids in Rainbow trout family. Genetics 93:961–973

    Google Scholar 

  • Thorgaard GH, Jazwin ME, Stier AR (1981) Polyploidy induced by heat shock in Rainbow trout. Trans Am Fish Soc 110:546–550

    Google Scholar 

  • Utter FM, Johnson OW, Thorgaard GH, Rabinovitch PS (1983) Measurements and potential applications of induced triploidy in Pacific salmon. Aquaculture 35:125–135

    Google Scholar 

  • Valenti RJ (1975) Induced polyploidy in Tilapia aurea (Steindachner) by means of temperature shock treatment. J Fish Biol 7:519–528

    Google Scholar 

  • Wester RC, Foote RH (1972) Ouabain effect on bovine spermatozoan motility and testosterone binding. Proc Soc Exp Biol Med 141:26–30

    Google Scholar 

  • Wolters WR, Libey GS, Chrisman CL (1982) Effect of triploid on growth and gonad development of Channal Catfish. Trans Am Fish Soc 111:102–105

    Google Scholar 

  • Zieve GW (1984) Nocodazole and cytochalasin D. induced tetraploidy in mammalian cells. Am J Physiol C 246:154

    Google Scholar 

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Communicated by E. J. Eisen

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Don, J., Avtalion, R.R. The induction of triploidy in Oreochromis aureus by heat shock. Theoret. Appl. Genetics 72, 186–192 (1986). https://doi.org/10.1007/BF00266991

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  • DOI: https://doi.org/10.1007/BF00266991

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