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金乌贼同工酶分析(英文) 被引量:4

Isozyme analysis of Sepia esculenta(Cephalopoda: Sepiidae)
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摘要 采用水平淀粉凝胶电泳技术对金乌贼(Sepia esculenta)同工酶的组织特异性及其山东日照近海群体的遗传结构进行研究。对金乌贼眼、鳃、肌肉、口球、肝脏、鳃心6种组织的19种同工酶进行分析,检测出PGDH、GPI、MPI、IDHP、SOD、ME、AAT、DIA、MDH、LDH、G3PDH、PGM共12种同工酶在几种组织中有较稳定而清晰的表达。结果表明,金乌贼同工酶的表达有明显的组织特异性。选择金乌贼3种组织(眼、口球、鳃心)进行同工酶分析,共记录了18个基因座位,其中3个基因座位LDH-2*、G3PDH-1*、PGM*呈多态,其多态座位比例为0.166 7(P0.99)和0.055 6(P0.95),平均观测杂合度和预期杂合度分别为0.015 9和0.014 3,平均有效等位基因数为1.020 1,表明日照近海金乌贼群体的遗传多样性较低。 Horizontal starch gel electrophoresis was used to investigate the tissue-specific and genetic structure of Sepia esculenta Hoyle, 1885 (Cephalopoda: Sepiidae). The specimens were collected from the coast of Rizhao, Shandong Province of China. A preliminary screening for 19 isozymes in six kinds of tissues (eye, branchia, mantle muscle, buccal bulb muscle, branchial heart, liver) was carried out using TC-7.0 buffer system. The results showed that the isozymes expression was highly tissue-specific in S. esculenta. Twelve isozymes (PGDH, GPI, MPI, IDHP, SOD, ME, AAT, DIA, MDH, LDH, G3PDH and PGM) and three kinds of tissues (eye, buccal bulb muscle and branchial heart) were .selected for genetic analysis of S. esculenta population. Of the eighteen putative enzyme-coding loci examined, three loci were polymorphlc, i.e., LDH-2^* , G3PDH-1 ^* and PGM ^* . The proportion of polymorphic loci was 0. 166 7 (P0.99) and 0.055 6 (P0.95).The average values of observed and expected heterozygosity were 0.015 9 and 0.014 3, respectively. The average effective number of alleles was 1.020 1. Analysis of S. esculenta in the present study revealed low levels of genetic variability.
出处 《中国水产科学》 CAS CSCD 北大核心 2005年第5期549-555,共7页 Journal of Fishery Sciences of China
基金 Supported by the Natural Science Foundation of Qingdao(04-2-JZ-80)and Key Technologies R&D Programof Shandong Province(2004GG2205110).
关键词 金乌贼 同工酶 组织特异性 遗传结构 Sepia esculenta isozyme tissue-specificity genetic structure
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  • 1Shaw, C.R.and Prasad, R.1970.Starch gel electrophoresis of enzymes-A complication of recipes [J].Biochemical Genetics, 4: 297-320.
  • 2Morizot, D.C., and M.E.Schmidt.1990.Starch gel electrophoresis and histochemicalvisualization of protein [A], in "Electrophoretic and Electro Focusing Technique in Fisheries Management" [C](ed.By D.H.Whitmore), CRC Press, Florida, 23-84.
  • 3May, B., 1992.Starch gel electrophoresis of isozymes [A].In: Molecular Genetic Analysis of Populations: A Practical Approach [C].(A.R.Hoelzel, ed.) Oxford Univ.Press, London.1-27, 271-280.
  • 4Shaklee J B, Allendorf F W, Morizot D C etal, 1990.Genetic Nomenclature for Protein-CodingLoci in Fish [J].Trans Amer Fish Soci, 119: 2-15.
  • 5Nei, M.,1972.Genetic distance between populations [J].The Amer.Nat., 106: 283-292
  • 6Katugin O N, 1993.Genetic variation in the squid Berryteuthis magister (Breey, 1913) (Oegopsida: Gonatiade) [A].Okutani T, O' dor R K, kubodera T, eds: Recent advances infisheries biology [C].Tokyo: Tokai University Press, 201-213.
  • 7O' Brien S J,Wildt D E, Bush M, et al., 1987.East African cheetahs: evidence for two population bottlenecks [J].Proc Natl Acad Sci.USA, 84: 508-511.
  • 8Ward R D, Skibinski D O F, Woodwork M, 1992.Protein heterozygosity, protein structure and taxonomic differentiation [J].Evol.Biol., 26: 73-159.
  • 9Fujio, Y., Yamanaka, R.and Smith, P.J.1983.Genetic variation in marine mollusks [J].Bull.Jap.Soc.Sci.Fish., 49: 1809-1817.
  • 10Pérez-Losada, M., Guerra A., Sanjuan A.1996.Allozyme electrophoretic technique and phylogenetic relationships in three species of Sepia (Cephalopoda: Sepiidae) [J].Comp.Biochem.Physiol.B, 114: 11~18.

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