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水稻卷叶突变新基因的遗传分析和初步定位

Genetic analysis and gene mapping of a new rolled leaf mutant in rice (Oryza sativa L.)

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【作者】 陈英之刘丕庆白德朗李容柏

【Author】 CHEN Ying-zhi1,LIU Pi-qing2,BAI De-lang3,LI Rong-bai1,4(1 Guangxi Key Laboratory of Subtropical Bio-resource Conservation and Utilization,Nanning 530005,China;2 Agricultural College,Guangxi University,Nanning 530005,China;3 China Hybrid Rice Research Center,Changsha,Hunan 410125,China;4 Guangxi Crop Genetic Improvement and Biotechnology Lab,Nanning 530007,China)

【机构】 广西亚热带资源保护利用重点实验室广西大学农学院国家杂交水稻工程研究中心广西作物遗传改良生物技术重点开放实验室

【摘要】 利用60Co-γ射线辐照水稻优良恢复系南花6号,获得一个水稻新型卷叶突变材料,整个生育期叶片表现为向内卷曲。经遗传分析表明,该突变性状受一对隐性基因控制。利用突变体南花6号/籼稻品种Dular F2群体中的141个卷叶单株进行基因定位,在双亲、卷叶和正常叶的DNA池中筛选到2个多态性标记RM285和RM342,并确定该基因位于水稻第9染色体长臂上,与前人报道的rl9(t)相距54.7 cM,是一个未曾报道的基因,暂时命名为rl13(t)。利用SSR标记将该基因定位于第9染色体RM285和RM342之间,遗传距离分别为6.74 cM和11.35 cM。类似于rl13(t)卷叶突变体表型未见报道,该研究结果对揭示卷叶机理及在株型改良应用中具有重要意义。

【Abstract】 In the present study,a new rolled leaf mutant was obtained from rice restoring line Nanhua 6 when treated with 60Co-γ ray.The mutant showed a rolled-leaf phenotype throughout the development stage.The F1,TC1,BC1 and F2 populations,derived from crosses between mutant Nanhua 6(P1),cultivar wild type Nanhua 6(P2) and Dular(P3) were used for genetic analysis.It was found that the mutant trait of rolled leaf was controlled by a pair of recessive gene.To determine the location of the gene,141 mutant-type F2(P1/P3) individuals derived from the cross of mutant Nanhua 6/Dular,were used and the bulked segregant analysis was carried out using DNA pools of mutant and wild-type.The screening with two polymorphic marker,viz.,RM285 and RM342 showed that the gene was located on the long arm of chromosome 9.The distance of the gene to reported gene rl9(t) was 54.7 cM,and it has not been reported elsewhere,therefore,temporarily named as rl13(t).By further gene mapping of RM285 and RM342,the gene was found to be located between RM285 and RM342 of the chromosome 9 with 6.74 and 11.35 cM genetic distances.Currently,the rolled-leaf genotype similar to rl13(t) has never been identified near the region.The results provide a basis for rl13(t) gene cloning and its functional analysis,and to study the mechanism related to rolled leaf and the improvement of plant-type.

【基金】 广西教育厅研究生创新基金项目(A31015);广西大学科研启动基金项目(DD702002)
  • 【文献出处】 广西农业科学 ,Guangxi Agricultural Sciences , 编辑部邮箱 ,2010年05期
  • 【分类号】S511.035.3
  • 【被引频次】10
  • 【下载频次】272
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