首页> 外文期刊>Indian Journal of Sericulture >Identification of genetic variations among silkworm races of Bombyx mori (L) through bio-molecular tools.
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Identification of genetic variations among silkworm races of Bombyx mori (L) through bio-molecular tools.

机译:通过生物分子工具鉴定家蚕(L)家蚕种之间的遗传变异。

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Silkworm races of Bombyx mori (L.) originated from different geographical regions exhibit distinct variations in phenotypic characters, especially in cocoon shape and colour. This information prompted us to study the genetic variations among eight multivoltine silkworm races applying biochemical and molecular markers of ISSR, RAPD and isozymes. These three markers provided sufficient polymorphism and genetic diversity. Highest level of genetic polymorphism was detected in ISSR marker analysis (95.83%) than in RAPD (77.77%) and isozyme (57.14%). The Marker Index (MI) values as a measure of genetic diversity was calculated for each marker and it was found high in ISSR based analysis (2.20) than RAPD (1.70) and isozyme (0.57). Dendrogram analysis showed two distinct cluster groups placing Hosa Mysore and Kolar Gold in one cluster and C.Nichi and Guangnong in another cluster. Hosa Mysore and Kolar Gold clustered together in all the marker analysis due to sharing of a common female parent i.e., Pure Mysore. C.Nichi and Guangnong shared a common cluster because of their exotic origin. Further, in RAPD and isozyme analysis, Sarupat and Moria were placed in a single cluster due to their common origin from Assam state (India). The polymorphism obtained from these three markers was also correlated using Mantel test and the results indicated a positive relationship (r=0.47) between ISSR and RAPD markers.
机译:源自不同地理区域的 Bombyx mori (L.)蚕种在表型特征上表现出明显的差异,尤其是在茧形和颜色上。这些信息促使我们利用ISSR,RAPD和同工酶的生化和分子标记研究了8个多级蚕的遗传变异。这三个标记提供了足够的多态性和遗传多样性。在ISSR标记分析中检测到最高水平的基因多态性(95.83%),高于RAPD(77.77%)和同工酶(57.14%)。对于每个标记,计算了标记指数(MI)值作为衡量遗传多样性的指标,在​​基于ISSR的分析(2.20)中发现它比RAPD(1.70)和同工酶(0.57)高。树状图分析显示两个不同的群集组,分别将Hosa Mysore和Kolar Gold放在一个群集中,将C.Nichi和Guangnong放在另一个群集中。由于共享一个共同的母本即Pure Mysore,Hosa Mysore和Kolar Gold在所有标记分析中均聚在一起。 C.Nichi和Guangnong由于异国血统而共享一个共同的集群。此外,在RAPD和同工酶分析中,Sarupat和Moria由于来自阿萨姆邦(印度)的共同起源而被放置在一个群集中。从这三个标记获得的多态性也使用Mantel检验进行关联,结果表明ISSR和RAPD标记之间存在正相关(r = 0.47)。

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