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人工雌核发育大黄鱼(Pseudosciaena crocea)的AFLP分析

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王晓清[1,2] 王志勇[1] 柳小春[2] 谢中国[2] 詹炜[2] 谢芳靖[1]

[1]集美大学水产学院,厦门361021 [2]湖南农业大学动物科技学院,长沙410128

海洋与湖沼
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国际标准刊号:ISSN 0029-814X
国内统一刊号:CN 37-1149

摘  要:

提要采用6对选择性扩增引物(E—AAG/M—CAG、E—AAG/M—CTC、E—ACA/M—CAA;E—ACG/M—CAT、E—AGG/M—CAA、E—AGG/M—CTA)对冷休克法诱导的大黄鱼雌核发育家系G1、G2和对照组C1、C2的鱼苗及其亲本进行了扩增片段长度多态性(AFLP)标记的比较分析。结果表明,6对引物共检出了33条雄亲特有条带(G1中13条,G2中20条)、31条雌亲特有条带(G1中16条。G2中15条)。家系G1的24尾鱼苗均无雄亲特有条带,雌核发育成功率为100%,G2家系中有3尾鱼苗各出现了不同数量的雄亲特有条带,属正常受精个体(12.5%),其雌核发育成功率为87.5%。两个家系平均雌核发育诱导成功率为93.75%。31条雌亲特有条带中有14条在雌核发育后代中出现了分离。对亲子间遗传关系的分析表明了雌核发育个体之间的遗传差异最小,与雌亲的亲缘关系最近。研究表明,雌核发育是促进基因纯合的一个有效途径。AFLP技术是鱼类雌核发育鉴定和遗传分析的有效方法。[著者文摘]

人工雌核发育,AFLP分析中图分类号Q346 国内外有关鱼类雌核发育诱导的成功报道很多(贾方钧等,2002;李胜忠等,1997;Lou et al,1984;Felip et al,2001;Levanduski et al,1990),但大部分研究仅注重诱导方法的探讨。有关雌核发育的后续研究较少。关于雌核发育的鉴定分析,过去多采用存在一定局限性的外部形态特征、染色体数目和生化遗传标记等常规方法。随着分子生物学的不断发展,目前已产生了大量能够探测高度遗传变异的RFLP、RAPD、AFLP、SSR等分子标记方法。AFLP(Amplified Fragments Length Poly—morphism)技术即扩增片段长度多态性,以其重复性好、特异性高等特点亦在水产动物的遗传分析中得到了广泛应用(Vos et al,1995;Liu et al,1998;Tariq,2004;Wang et al,2000)。
Oceanologia Et Limnologia Sinica

分 类 号:

Q346

相关文章:

参考文献(15篇) 被引情况(1篇) 耦合文献(12篇)  主题相关

[参考文献]

AFLP ANALYSIS OF ARTIFICIAL GYNOGENESIS IN PSEUDOSCIAENA CROCEA

WANG Xiao-Qing, WANG Zhi-Yong, LIU Xiao-Chun, XIE Zhong-Guo, ZHAN Wei , XIE Fang-Jing (1. Fisheries College, Jimei University, Xiamen, 361021 ; 2. College of Animal Science and Technology, Hunan Agricultural University, Changsha , 410128)

Abstract:

A comparative analysis of AFLP was performed by using 6 pairs of selective primers ( E-AAG/ M-CAG, E-AAG/M-CTC, E-ACA/M-CAA; E-ACG/M-CAT, E-AGG/M-CAA, E-AGG/M-CTA) in Pseudociaena crocea fries from two groups(G1, G2)of the gynogens induced by cool-shock method, two groups of contrast (C1, C2)and their parents. The similarity coefficient and genetic distance among gynogenetic offspring, the contrast(hybrid)and their parents were calculated along with phylogenetic clustering analysis. A total of 33 special male bands( 13 in G1, 20 in G2) ,and 31 special female bands( 16 in G1, 15 in G2)were revealed in 6 pairs of primers. The amplification showed no male gene in 24 fries of family G1, suggesting that they all derived from gynogenesis. The successful induction ratio was 100%. Different special male bands appeared in 3 individuals of family G2, suggesting the origin of normal fertilization( 12.5% ). Its successful induction ratio was 87.5%. The average gynogenetic ratio of the two families was 93.75%. Thirteen maternal loci(8 in G1, 5 in G2)were homozygotic. 14 of 31 special female bands were separated in the gynogens indicative of heterozygosity. The homozygosity ratio of the offspring from the two families was 87.5% and 76.2% in average of 81.9% , whereas it was zero in their contrast. It is clear that the similarity coefficient among gynogens of two families was the largest, or the genetic distance among gynogens was the shortest among the hybrids of their contrast. The relation of the gynogens was the closest to the female parent but male one. Therefore, gynogenesis analysis with AFLP marker technique is practical in gene purification, verification and other genetic analyses.[著者文摘]

Key words:

Large yellow croaker, Artificial gynogenesis, AFLP analysis

收稿日期: 2005-10-12
修订日期: 2005-12-15

基金资助:

国家自然科学基金项目,30271037号;国家863计划项目,2002AA603021号;福建省农业科技重大专项.2004NZ031号;集美大学创新科研团队基金,2005-2008.

作者简介:

王晓清,副教授,博士生,E-mail:wangxiao8258@126.com. 通讯作者:王志勇,教授,博导,E-mail:zywang@jmu.edu.cn

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