DOI QR코드

DOI QR Code

A comparative analysis of cell cycles in diploid and induced triploid tissues in marine medaka(Oryzias dancena)

해산송사리(Oryzias dancena) 2배체와 유도 3배체 조직의 세포주기 비교

  • Park, In-Seok (Division of Marine Bioscience, College of Ocean Science and Technology, Korea Maritime & Ocean University)
  • 박인석 (한국해양대학교 해양과학기술대학 해양생명과학부)
  • Received : 2019.11.26
  • Accepted : 2019.12.17
  • Published : 2019.12.31

Abstract

The aim of this study was to conduct a comparative analysis of the diploid and induced triploid cell cycles in marine medaka, Oryzias dancena, tissues. The mean fraction of cells in the G1, S, and G2+M phases was 85.5%, 7.6%, and 6.9%, respectively, in the tail fin tissues of diploid fish and 91.2%, 3.6%, and 5.2%, respectively, in those of induced triploid fish. The mean fraction of cells in the G1, S, and G2+M phases were 78.4%, 10.6%, and 11.0%, respectively, in the liver tissues of diploid fish; 86.2%, 5.9%, and 7.9%, respectively, in those of induced triploid; 79.3%, 9.4%, and 11.3%, respectively, in the gill tissues of diploid fish; and 85.7%, 5.4%, and 8.9%, respectively, in the induced triploid fish. The differences among the tissues were statistically significant within both the diploid and induced triploid fish (p<0.05). Mitosis was more active in each tissue of the diploid fish than in the corresponding tissues of the induced triploid fish and mitosis was more active in the liver and gill tissues than in the tail fin tissues in both the diploid and induced triploid marine medaka.

해산송사리, Oryzias dancena 2배체와 유도 3배체 각 조직에서의 세포주기를 비교, 분석하였다. G1, S, G2+M기의 분포 빈도에서 꼬리지느러미인 경우 2배체에서는 85.8%, 7.6% 및 6.9%이었으며 유도 3배체에서는 91.2%, 3.6% 및 5.2%이었다. 간 조직인 경우 2배체에서는 78.4%, 10.6%, 및 11.0%이었으며 유도 3배체는 86.2%, 5.9% 및 7.9%이었다. 아가미 조직인 경우 2배체에서는 79.3%, 9.4% 및 11.3%이었으며 유도 3배체는 85.7%, 5.4% 및 8.9%이었다. 2배체와 유도 3배체에서 조직 간 세포 주기 빈도에서 유의한 차이가 있었다(p<0.05). Mitosis (체세포분열)은 유도 3배체에 비해 2배체가 더욱 활성이 있었으며, 이러한 체세포분열은 2배체와 유도 3배체 모두에서 꼬리지느러미 조직 보다는 간 조직과 아가미 조직에서 더욱 왕성하였다.

Keywords

References

  1. Abraham D. 2011. "Oryzias dancena". The IUCN Red List of Threated Species. eT172326A6868382. International Union for Conservation of Nature. Gland, Switzerland.
  2. Cho YS, SY Lee, DS Kim and YK Nam. 2010a. Tolerance capacity to salinity change in adult and larva of Oryzias dancena, a euryhaline medaka. Korean J. Ichthyol. 22:9-16.
  3. Cho YS, SY Lee, DS Kim and YK Nam. 2010b. Spawning performance, embryonic development and early viability under different salinity conditions in a euryhaline medaka species, Oryzias dancena. Korean J. Ichthyol. 22:25-33.
  4. Cho YS, SY Lee, DS Kim and YK Nam. 2012. Characterization of stable fluorescent transgenic marine medaka (Oryzias dancena) lines carrying red fluorescent protein gene driven by myosin light chain 2 promoter. Transgenic Res. 22:849-859. https://doi.org/10.1007/s11248-012-9675-2
  5. Dean PN and J Jett. 1974. Mathematical analysis of DNA distributions derived from flow microfluorometry. J. Cell Biol. 60:523-527. https://doi.org/10.1083/jcb.60.2.523
  6. Dunham RA and RH Devlin. 1999. Comparison of traditional breeding and transgenesis in farmed fish with implications for growth enhancement and fitness. pp. 209-229. In Transgenic Animals in Agriculture (Murray JD, GB Anderson, AM Oberbauer and MN McGloughlin eds.). CAB International, New York.
  7. Estevam J, H Danaee, R Liu, J Ecsedy, W Trepicchio and T Wyant. 2011. Validation of a flow cytometry based G2M delay cell cycle assay for use in evaluating the pharmacodynamic response to Aurora A inhibition. J. Immunol. Methods 363:135-142. https://doi.org/10.1016/j.jim.2010.09.021
  8. Gil HW, TH Lee, HJ Han and IS Park. 2017. Comparative analysis of tissue and cell cycle on the for eastern catfish, Silurus asotus between diploid and triploid. Dev. Reprod. 21:193-204. https://doi.org/10.12717/DR.2017.21.2.193
  9. Goo IB, JH Im, HW Gil, SG Lim and IS Park. 2015. Comparison of cell and nuclear size difference between diploid and induced triploid in marine medaka, Oryzias dancena. Dev. Reprod. 19:127-134. https://doi.org/10.12717/DR.2015.19.3.127
  10. Im JH, HW Gill, TH Lee, HJ Kong, CM Ahn, BS Kim, DS Kim, CI Zhang and IS Park. 2016. Morphometric characteristics and fin dimorphism between male and female on the marine medaka, Oryzias dancena. Dev. Reprod. 20:331-347. https://doi.org/10.12717/DR.2016.20.4.331
  11. Inoue K and Y Takei. 2003. Asian medaka fishes offer new models for studying mechanisms of seawater adaptation. Comp. Biochem. Physiol. B 136:635-645. https://doi.org/10.1016/S1096-4959(03)00204-5
  12. Kang CK, SC Tsai, TH Lee and PP Hwang. 2008. Differential expression of branchial $Na^+/K^+$ -ATPase of two medaka species (Oryzias latipes) and (Oryzias dancena), with different salinity tolerances acclimated to fresh water, brackish water and seawater. Comp. Biochem. Physiol. A 151:566-576. https://doi.org/10.1016/j.cbpa.2008.07.020
  13. Kim DS, HJ Cho, IS Park, GC Choi and YK Nam. 2001. Cytogenetic traits and gonad development of induced triploidy in far eastern catfish, Silurus asotus. Korean J. Genetics 23:55-62.
  14. Kim DS, JY Jo and TY Lee. 1994. Introduction of triploidy in mud loach, Misgurnus mizolepis and its effect on gonad development and growth. Aquaculture 120:263-270. https://doi.org/10.1016/0044-8486(94)90083-3
  15. Lee HB, DS Kim, HW Gil and IS Park. 2018. Physiological response of diploid and triploid far eastern catfish, Silurus asotus to water temperature stress. Dev. Reprod. 22:165-174. https://doi.org/10.12717/DR.2018.22.2.165
  16. Lim HB, DS Kim, HW Gil and IS Park. 2018. Physiological responses of diploid and triploid far eastern catfish, Silurus asotus to water temperature stress. Dev. Reprod. 22:165-174. https://doi.org/10.12717/DR.2018.22.2.165
  17. Lim SG, HK Han, KS Kim, BS Kim, HM Baek, IS Park and HW Gil. 2012. Observations on the reproductive behavior of the marine medaka, Oryzias dancena. Korean J. Ichthyol. 24:220-226.
  18. Lim SY, HW Gil and IS Park. 2017. Change of various characteristics between spawning and non-spawning season in diploid and induced triploid Far Eastern catfish, Silurus asotus. Dev. Reprod. 21:275-286. https://doi.org/10.12717/DR.2017.21.3.275
  19. Lincoln RF and V Bye. 1984. Triploid rainbows show commercial potential. Fish Farmer 7:30-32.
  20. Park IS and CY Choi. 2018. Occurrence of amitosis-like nuclear division in erythrocytes of induced triploid Far Eastern catfish, Silurus asotus and marine medaka, Oryzias dancena. JFMSE 30:1519-1527. https://doi.org/10.13000/JFMSE.2018.10.30.5.1519
  21. Park IS and DS Kim. 2000. Comparison of some tissues in diploid and triploid hybrid between mud loach, Misgurnus mizolepis and cyprinid loach, M. anguillicaudatus. Dev. Reprod. 4:19-28.
  22. Park IS and HB Kim. 1994. Induction of triploid cherry salmon, Oncorhynchus masou. J. Aquacult. 7:207-223.
  23. Park IS and HW Gil. 2018. Comparative analysis of fluctuating asymmetry between ploidy and sex in marine medaka, Oryzias dancena. Dev. Reprod. 22:275-281. https://doi.org/10.12717/DR.2018.22.3.275
  24. Park IS and KY Park. 1995. Haematological and physiological characteristics of diploid and triploid in cherry salmon, Oncorhynchus masou. J. Aquacult. 8:21-29.
  25. Park IS, HW Gil and DS Kim. 2018. Morphometric characteristics of diploid and triploid marine medaka, Oryzias dancena. Dev. Reprod. 22:183-192. https://doi.org/10.12717/DR.2018.22.2.183
  26. Park IS, HW Gil, TH Lee, YK Nam and DS Kim. 2016a. Comparative study of growth and gonad maturation in diploid and triploid marine medaka, Oryzias dancena. Dev. Reprod. 20:305-314. https://doi.org/10.12717/DR.2016.20.4.305
  27. Park IS, HW Gil, TH Lee, YK Nam, MG Ko and DS Kim. 2016b. Cytogenetic study of diploid and triploid marine medaka, Oryzias dancena. Korean J. Ichthyol. 28:215-222.
  28. Park IS, SJ Park, HW Gil, YK Nam and DS Kim. 2011. Anesthetic effects of clove oil and lidocaine-HCl on marine medaka, Oryzias dancena. Lab Anim. 40:45-51. https://doi.org/10.1038/laban0211-45
  29. Seol DW, SY Im, WJ Hur, MO Park, DS Kim, JY Jo and IS Park. 2008. Haematological parameters and respiratory function in diploid and triploid Far Eastern catfish, Silurus asotus. Genes Genom. 30:205-213.
  30. Sezaki K, S Watbe and K Hashimoto. 1988. Haematological parameters and erythrocyte enzyme activities associated with increase in ploidy status of the spinous loach, Cobitis biwae Jordan and Synder. J. Fish Biol. 32:149-150. https://doi.org/10.1111/j.1095-8649.1988.tb05343.x
  31. Thorgaard GH. 1983. Chromosome set manipulation and sex control in fish. pp. 405-434. In Fish Physiology (Hoar WS, DJ Randall and EM Donaldson eds.), Vol. IX B. Academic Press, New York.
  32. Ueno K. 1984. Induction of triploid carp and their haematological characteristics. Jpn. J. Genet. 59:585-591. https://doi.org/10.1266/jjg.59.585
  33. Vanparys C, M Maras, M Lenjou, J Robbens, D van Bockstaele, R Blust and W de Coen. 2006. Flow cytometric cell cycle analysis allows for rapid screening of estrogenicity in MCF-7 breast cancer cells. Toxicol. Vitro 20:1238-1248. https://doi.org/10.1016/j.tiv.2006.05.002
  34. Wolters WR, GS Libey and CL Chrisman. 1982. Effects of triploidy on growth and gonad development of channel catfish. Trans. Am. Fish. Soc. 111:102-105. https://doi.org/10.1577/1548-8659(1982)111@@<@@102:eotoga@@>@@2.0.co;2
  35. Yoo GY, TH Lee, HW Gil, SG Lim and IS Park. 2018. Cytogenetic analysis of hybrids and hybrid triploids between the river puffer, Takifugu obscurus, and the tiger puffer, Takifugu rubripes. Aquacult. Res. 49:637-650. https://doi.org/10.1111/are.13493