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Monosex in Aquaculture

  • Tomer Ventura
Chapter
Part of the Results and Problems in Cell Differentiation book series (RESULTS, volume 65)

Abstract

Monosex refers to the culture of either all-male or all-female populations, a sought after approach in aquaculture. This chapter reviews the advantages of monosex population culture and details the mechanisms to achieve it based on different modes of sex determination and sexual differentiation. A recent case study for an aquaculture biotechnology based on sexual manipulation in crustaceans serves in this chapter to identify the key elements for a successful application. This application which makes use of RNA interference with a key regulating hormone opens the pathway toward environmentally friendly applications in fish and additional aquacultured species. This chapter portrays the state of the art in sexual manipulations in aquacultured species, starting with vertebrate species, followed by the case study of the crustacean species and discussion on how the techniques used in this study are applicable for other species.

References

  1. Bao B, Garverick HA (1998) Expression of steroidogenic enzyme and gonadotropin receptor genes in bovine follicles during ovarian follicular waves: a review. J Anim Sci 76(7):1903–1921CrossRefGoogle Scholar
  2. Budd A, Banh Q, Domingos J, Jerry D (2015) Sex control in fish: approaches, challenges and opportunities for aquaculture. J Mar Sci Eng 3(2):329CrossRefGoogle Scholar
  3. Chandler JC, Aizen J, Elizur A, Hollander-Cohen L, Battaglene S, Ventura T (2015) Discovery of a novel insulin-like peptide and insulin binding proteins in the Eastern rock lobster Sagmariasus verreauxi. Gen Comp Endocrinol 215:76–87CrossRefGoogle Scholar
  4. Cohen D, Sagi A, Ra'anan Z, Zohar G (1988) The production of Macrobrachium rosenbergii in monosex populations: III—yield characteristics under intensive monoculture conditions in earthen ponds. Isr J Aquacult Bamidgeh 40:57–63Google Scholar
  5. Devlin RH, Nagahama Y (2002) Sex determination and sex differentiation in fish: an overview of genetic, physiological, and environmental influences. Aquaculture 208(3–4):191–364CrossRefGoogle Scholar
  6. Malecha SR, Nevin PA, Ha P, Barck LE, Lamadrid-Rose Y, Masuno S, Hedgecock D (1992) Sex-ratios and sex-determination in progeny from crosses of surgically sex-reversed freshwater prawns, Macrobrachium rosenbergii. Aquaculture 105:201–218CrossRefGoogle Scholar
  7. Megbowon I, Mojekwu TO (2014) Tilapia sex reversal using methyl testosterone (MT) and its effect on fish, man and environment. Biotechnology 13:213–216CrossRefGoogle Scholar
  8. Munsterberg A, Lovell-Badge R (1991) Expression of the mouse anti-mullerian hormone gene suggests a role in both male and female sexual differentiation. Development 113(2):613–624PubMedGoogle Scholar
  9. Nair CM, Salin KR, Raju MS, Sebastian M (2006) Economic analysis of monosex culture of giant freshwater prawn (Macrobrachium rosenbergii De Man): a case study. Aquac Res 37(9):949–954CrossRefGoogle Scholar
  10. Pandia TJ (2012) Genetic sex differentiation in fish. CRC Press, FloridaCrossRefGoogle Scholar
  11. Raymond CS, Shamu CE, Shen MM, Seifert KJ, Hirsch B, Hodgkin J, Zarkower D (1998) Evidence for evolutionary conservation of sex-determining genes. Nature 391(6668):691–695CrossRefGoogle Scholar
  12. Sagi A, Cohen D (1990) Growth, maturation and progeny of sex-reversed Macrobrachium rosenbergii males. World Aquacult 21:87–90Google Scholar
  13. Sandra G-E, Norma M-M (2009) Sexual determination and differentiation in teleost fish. Rev Fish Biol Fish 20(1):101–121CrossRefGoogle Scholar
  14. Suzuki MG, Ohbayashi F, Mita K, Shimada T (2001) The mechanism of sex-specific splicing at the doublesex gene is different between Drosophila melanogaster and Bombyx mori. Insect Biochem Mol Biol 31(12):1201–1211CrossRefGoogle Scholar
  15. Ventura T, Sagi A (2012) The insulin-like androgenic gland hormone in crustaceans: from a single gene silencing to a wide array of sexual manipulation-based biotechnologies. Biotechnol Adv 30(6):1543–1550CrossRefGoogle Scholar
  16. Ventura T, Manor R, Aflalo ED, Weil S, Raviv S, Glazer L, Sagi A (2009) Temporal silencing of an androgenic gland-specific insulin-like gene affecting phenotypical gender differences and spermatogenesis. Endocrinology 150(3):1278–1286CrossRefGoogle Scholar
  17. Ventura T, Aflalo ED, Weil S, Kashkush K, Sagi A (2011a) Isolation and characterization of a female-specific DNA marker in the giant freshwater prawn Macrobrachium rosenbergii. Heredity 107:456–461CrossRefGoogle Scholar
  18. Ventura T, Rosen O, Sagi A (2011b) From the discovery of the crustacean androgenic gland to the insulin-like hormone in six decades. Gen Comp Endocrinol 173(3):381–388CrossRefGoogle Scholar
  19. Ventura T, Manor R, Aflalo ED, Weil S, Rosen O, Sagi A (2012) Timing sexual differentiation: full functional sex reversal achieved through silencing of a single insulin-like gene in the prawn, Macrobrachium rosenbergii. Biol Reprod 86(3):1–6CrossRefGoogle Scholar
  20. Ventura T, Fitzgibbon Q, Battaglene S, Sagi A, Elizur A (2014) Identification and characterization of androgenic gland specific insulin-like peptide-encoding transcripts in two spiny lobster species: Sagmariasus verreauxi and Jasus edwardsii. Gen Comp Endocrinol 214:126–133CrossRefGoogle Scholar

Copyright information

© Springer International Publishing AG, part of Springer Nature 2018

Authors and Affiliations

  1. 1.School of Science and EngineeringUniversity of the Sunshine CoastMaroochydoreAustralia

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