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利用SSR标记对家蚕浓核病不敏感基因nsd-Z进行连锁和定位分析。

Linkage and mapping analyses of the densonucleosis non-susceptible gene nsd-Z in the silkworm Bombyx mori using SSR markers.

作者信息

Li Muwang, Guo Qiuhong, Hou Chengxiang, Miao Xuexia, Xu Anying, Guo Xijie, Huang Yongping

机构信息

Sericultural Research Institute, Chinese Academy of Agricultural Sciences, Zhenjiang 212018, PR China.

出版信息

Genome. 2006 Apr;49(4):397-402. doi: 10.1139/g05-125.

Abstract

In the silkworm Bombyx mori, non-susceptibility to the Zhenjiang (China) strain of the densonucleosis virus (DNV-Z) is controlled by the recessive gene nsd-Z (non-susceptible to DNV-Z), which is located on chromosome 15. Owing to a lack of crossing over in females, reciprocal backcrossed F1 (BC1) progeny were used for linkage analysis and mapping of the nsd-Z gene using silkworm strains Js and L10, which are classified as being highly susceptible and non-susceptible to DNV-Z, respectively. BC1 larvae were inoculated with the DNV-Z virus at the first instar, and DNA was extracted from the individual surviving pupae and analyzed for simple sequence repeat (SSR) markers. The nsd-Z gene was found to be linked to 7 SSR markers, as all the surviving larvae in the BC1female (F1female x L10male) showed the homozygous profile of strain L10, and the sick larvae in the BC1female (F1female x L10male) showed the heterozygous profile of Js x L10 F1 hybrids. Using a reciprocal BC1male (L101female x F1male) cross, we constructed a linkage map of 80.6 cM, with nsd-Z mapped at 30 cM and the closest SSR marker at a distance of 4.4 cM.

摘要

在家蚕中,对中国镇江株浓核症病毒(DNV-Z)的不敏感性由位于第15号染色体上的隐性基因nsd-Z(对DNV-Z不敏感)控制。由于雌性家蚕缺乏交叉互换,因此利用对DNV-Z分别表现为高敏感性和不敏感性的家蚕品系Js和L10,通过正反交回交F1(BC1)后代进行nsd-Z基因的连锁分析和定位。在一龄期给BC1幼虫接种DNV-Z病毒,从存活的蛹个体中提取DNA,并分析简单序列重复(SSR)标记。发现nsd-Z基因与7个SSR标记连锁,因为BC1雌性(F1雌性×L10雄性)中所有存活幼虫均表现出L10品系的纯合谱型,而BC1雌性(F1雌性×L10雄性)中的患病幼虫表现出Js×L10 F1杂种的杂合谱型。通过正反交BC1雄性(L10雌性×F1雄性)杂交,构建了一个80.6厘摩的连锁图谱,其中nsd-Z定位于30厘摩处,最近的SSR标记距离为4.4厘摩。

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