中国水产科学
中國水產科學
중국수산과학
Journal of Fishery Sciences of China
2005年
5期
549-555
,共7页
金乌贼%同工酶%组织特异性%遗传结构
金烏賊%同工酶%組織特異性%遺傳結構
금오적%동공매%조직특이성%유전결구
Sepia esculenta%isozyme%tissue-specificity%genetic structure
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.
採用水平澱粉凝膠電泳技術對金烏賊(Sepia esculenta)同工酶的組織特異性及其山東日照近海群體的遺傳結構進行研究.對金烏賊眼、鰓、肌肉、口毬、肝髒、鰓心6種組織的19種同工酶進行分析,檢測齣PGDH、GPI、MPI、IDHP、SOD、ME、AAT、DIA、MDH、LDH、G3PDH、PGM共12種同工酶在幾種組織中有較穩定而清晰的錶達.結果錶明,金烏賊同工酶的錶達有明顯的組織特異性.選擇金烏賊3種組織(眼、口毬、鰓心)進行同工酶分析,共記錄瞭18箇基因座位,其中3箇基因座位LDH-2*、G3PDH-1*、PGM*呈多態,其多態座位比例為0.166 7(P0.99)和0.055 6(P0.95),平均觀測雜閤度和預期雜閤度分彆為0.015 9和0.014 3,平均有效等位基因數為1.020 1,錶明日照近海金烏賊群體的遺傳多樣性較低.
채용수평정분응효전영기술대금오적(Sepia esculenta)동공매적조직특이성급기산동일조근해군체적유전결구진행연구.대금오적안、새、기육、구구、간장、새심6충조직적19충동공매진행분석,검측출PGDH、GPI、MPI、IDHP、SOD、ME、AAT、DIA、MDH、LDH、G3PDH、PGM공12충동공매재궤충조직중유교은정이청석적표체.결과표명,금오적동공매적표체유명현적조직특이성.선택금오적3충조직(안、구구、새심)진행동공매분석,공기록료18개기인좌위,기중3개기인좌위LDH-2*、G3PDH-1*、PGM*정다태,기다태좌위비례위0.166 7(P0.99)화0.055 6(P0.95),평균관측잡합도화예기잡합도분별위0.015 9화0.014 3,평균유효등위기인수위1.020 1,표명일조근해금오적군체적유전다양성교저.
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 screeninng 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 polymorphic, 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.