基于RAPD分子标记的鲫鲫5个雌化无性系遗传异质性分析

L Zhou, Y Wang, J F Gui
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引用次数: 71

摘要

异育银鲫(Carassius auratus gibelio)由于其特殊的遗传背景和繁殖方式,是研究进化遗传学和选择育种的独特模型系统。采用随机扩增多态性DNA (RAPD)技术对5个雌性生殖克隆进行分析,引物长度为10个核苷酸。26条引物扩增良好,条带模式可复制,24条引物为多态。在每个克隆中观察到几乎相同的条带模式,表明每个克隆可能由于其雌核发生而具有特定的模式。相比之下,5个无性系的RAPD模式存在差异。基于3744个可区分片段(每个个体156个),采用UPGMA聚类分析构建了系统发育树。5个克隆内和克隆间的平均遗传距离清楚地表明它们的克隆内同质性、克隆间异质性和系统发育关系。无性系A和无性系P亲缘关系最密切,无性系D与无性系E或无性系f差异最大。除去5个无性系的单态条带,从24条引物中共获得88个多态性片段。大多数与多态片段相对应的引物扩增出一个克隆或两个、三个或四个克隆共享的可复制标记。几个引物(如Opj-1、Opj-7和Opp-10)产生了丰富的条带模式,可以用来区分五个克隆。还鉴定了一个或两个克隆的特异性标记。本研究中发现的RAPD标记可能对进化遗传学和选择育种研究有益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of genetic heterogeneity among five gynogenetic clones of silver crucian carp, Carassius auratus gibelio Bloch, based on detection of RAPD molecular markers.

The gynogenetic silver crucian carp, Carassius auratus gibelio, is a unique model system for studying evolutionary genetics and selective breeding, owing to its specific genetic background and reproductive modes. Five gynogenetic clones were analyzed by the random amplified polymorphic DNA (RAPD) technique, using 30 10-nucleotide-long primers. Twenty-six primers produced well-amplified DNA fragments with reproducible banding patterns, and 24 primers were polymorphic. Nearly identical banding patterns were observed among individuals within each clone, suggesting that each clone might possess a specific pattern owing to its gynogenesis. In contrast, the RAPD patterns of the five clones differed from each other. A phylogenetic tree was constructed using UPGMA cluster analysis based on a total of 3,744 distinguishable fragments (156 per individual). Average genetic distances within and among the five clones clearly indicated their intraclonal homogeneity, interclonal heterogeneity, and phylogenetic relationships. Clones A and P were the most closely related, whereas the most divergence was seen between clone D and clone E or F. A total of 88 polymorphic fragments were scored from 24 primers after excluding bands that were monomorphic for the five clones. Most primers corresponding to the polymorphic fragments amplified reproducible markers specific for one clone or that were shared by two, three, or four clones. Several primers (e.g., Opj-1, Opj-7, and Opp-10) produced abundant banding patterns that could be used to discriminate between the five clones. Markers specific for one or two clones were also identified. The RAPD markers identified in this study will likely benefit evolutionary genetics and selective breeding studies.

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