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皱纹盘鲍(Haliotis discus hannai Ino)的初步遗传连锁图谱。

A preliminary genetic linkage map of the Pacific abalone Haliotis discus hannai Ino.

作者信息

Liu Xiande, Liu Xiao, Guo Ximing, Gao Qikang, Zhao Hongen, Zhang Guofan

机构信息

Institute of Oceanology, Chinese Academy of Sciences, Qingdao, Shandong, 266071, China.

出版信息

Mar Biotechnol (NY). 2006 Jul-Aug;8(4):386-97. doi: 10.1007/s10126-005-6133-7. Epub 2006 Jun 2.

DOI:10.1007/s10126-005-6133-7
PMID:16779713
Abstract

Preliminary genetic linkage maps were constructed for the Pacific abalone (Haliotis discus hannai Ino) using amplified fragment length polymorphism (AFLP), randomly amplified polymorphic DNA (RAPD), and microsatellite markers segregating in a F(1) family. Nine microsatellite loci, 41 RAPD, and 2688 AFLP markers were genotyped in the parents and 86 progeny of the mapping family. Among the 2738 markers, 384 (including 365 AFLP markers, 10 RAPD markers, and 9 microsatellite loci) were polymorphic and segregated in one or both parents: 241 in the female and 146 in the male. The majority of these markers, 232 in the female and 134 in the male, segregated according to the expected 1:1 Mendelian ratio (alpha = 0.05). Two genetic linkage maps were constructed using markers segregating in the female or the male parent. The female framework map consisted of 119 markers in 22 linkage groups, covering 1773.6 cM with an average intermarker space of 18.3 cM. The male framework map contained 94 markers in 19 linkage groups, spanning 1365.9 cM with an average intermarker space of 18.2 cM. The sex determination locus was mapped to the male map but not to the female map, suggesting a XY-male determination mechanism. Distorted markers showing excess of homozygotes were mapped in clusters, probably because of their linkage to a gene that is incompatible between two parental populations.

摘要

利用扩增片段长度多态性(AFLP)、随机扩增多态性DNA(RAPD)和在一个F(1)家系中分离的微卫星标记,构建了皱纹盘鲍(Haliotis discus hannai Ino)的初步遗传连锁图谱。对作图家系的亲本和86个后代的9个微卫星位点、41个RAPD和2688个AFLP标记进行了基因分型。在这2738个标记中,有384个(包括365个AFLP标记、10个RAPD标记和9个微卫星位点)具有多态性,并在一个或两个亲本中分离:雌性中有241个,雄性中有146个。这些标记中的大多数,雌性中有232个,雄性中有134个,按照预期的1:1孟德尔比率分离(α = 0.05)。利用在雌性或雄性亲本中分离的标记构建了两个遗传连锁图谱。雌性框架图谱由22个连锁群中的119个标记组成,覆盖1773.6 cM,标记间平均间距为18.3 cM。雄性框架图谱包含19个连锁群中的94个标记,跨度为1365.9 cM,标记间平均间距为18.2 cM。性别决定位点定位于雄性图谱而不是雌性图谱,表明存在XY雄性决定机制。显示纯合子过量的扭曲标记成簇定位,可能是因为它们与两个亲本群体之间不相容的一个基因连锁。

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