Suppr超能文献

一个水稻褐飞虱抗性基因的分子定位与遗传分析

Molecular mapping and genetic analysis of a rice brown planthopper (Nilaparvata lugens Stål) resistance gene.

作者信息

Yang Haiyuan, Ren Xiang, Weng Qingmei, Zhu Lili, He Guangcun

机构信息

Key Laboratory of Ministry of Education for Plant Development Biology, Wuhan University, College of Life Sciences, PR China.

出版信息

Hereditas. 2002;136(1):39-43. doi: 10.1034/j.1601-5223.2002.1360106.x.

Abstract

The brown planthopper (BPH), Nilaparvata lugens Stål, is a serious insect pest of rice (Oryza saliva L.). We have determined the chromosomal location of a BPH resistance gene in rice using SSR and RFLP techniques. A rice line 'B14', derived from the wild rice Oryza latifolia, showed high resistance to BPH. For tagging the resistance gene in 'B14X', an F2 population and a recombinant inbred (RI) population from a cross between Taichung Native 1 and 'B14' were developed and evaluated for BPH resistance. The results showed that a single dominant gene controlled the resistance of 'B14' to BPH. Bulked segregant SSR analysis was employed for identification of DNA markers linked to the resistance gene. From the survey of 302 SSR primer pairs, three SSR (RM335, RM261, RM185) markers linked to the resistance gene were identified. The closest SSR marker RM261 was linked to the resistance gene at a distance of 1.8 cM. Regions surrounding the resistance gene and the SSR markers were examined with additional RFLP markers on chromosome 4 to define the location of the resistance gene. Linkage of RFLP markers C820, R288, C946 with the resistance gene further confirmed its location on the short arm of chromosome 4. Closely linked DNA markers will facilitate selection for resistant lines in breeding programs and provide the basis for map-based cloning of this resistance gene.

摘要

褐飞虱(Nilaparvata lugens Stål)是水稻(Oryza saliva L.)的一种严重害虫。我们利用SSR和RFLP技术确定了水稻中一个抗褐飞虱基因的染色体定位。一个源自野生稻宽叶野生稻的水稻品系“B14”对褐飞虱表现出高抗性。为了标记“B14X”中的抗性基因,构建了台中本地1号与“B14”杂交的F2群体和重组自交(RI)群体,并对其褐飞虱抗性进行了评估。结果表明,一个显性单基因控制“B14”对褐飞虱的抗性。采用混合分离群体SSR分析法鉴定与抗性基因连锁的DNA标记。通过对302对SSR引物对的筛选,鉴定出3个与抗性基因连锁的SSR(RM335、RM261、RM185)标记。最紧密的SSR标记RM261与抗性基因的连锁距离为1.8 cM。利用第4染色体上的其他RFLP标记对抗性基因及SSR标记周围区域进行检测,以确定抗性基因的位置。RFLP标记C820、R288、C946与抗性基因的连锁进一步证实了其位于第4染色体短臂上。紧密连锁的DNA标记将有助于在育种计划中选择抗性品系,并为该抗性基因的图位克隆提供基础。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验