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水稻窄叶突变体zy103突变基因鉴定
引用本文:杨永义,周学标,姚方印,侯恒军,孙召文,袁守江,张洪瑞,李广贤.水稻窄叶突变体zy103突变基因鉴定[J].核农学报,2019,33(3):421-431.
作者姓名:杨永义  周学标  姚方印  侯恒军  孙召文  袁守江  张洪瑞  李广贤
作者单位:1 山东省水稻研究所,山东 济南 250100; 2 山东省农作物种质资源中心,山东 济南 250100; 3 山东省农业科学院高新技术研究中心,山东 济南 250100; 4 济宁市任城区农业局, 山东 济宁 272000
基金项目:国家重点实验室开放课题项目(150102),山东省现代农业产业技术体系水稻产业创新团队建设项目(SDAIT-01-016-01),山东省农业科学院农业科技创新工程(CXGC2016A11)
摘    要:为通过叶形相关基因定位与克隆解析水稻叶形变异的分子机制,本研究以籼稻品种9311与粳稻品种豫粳6号的杂交F7株系中发现的窄叶突变体zy103为试验材料,应用(zy103/9311)F2、F3分离群体对窄叶基因进行精细定位及候选基因预测。表型分析表明,突变体zy103出现全生育期叶片变窄微卷、株高及结实率降低、成熟种子弯曲变形等变异表型。遗传分析和基因定位结果表明,突变体zy103受1对隐性核基因控制,该基因被定位于第12号染色体195.4 kb的区间内,此区间内共预测了28个编码基因。对区间内与水稻叶形态建成相关的OsCSLD4(LOC_Os12g36890.1)基因进行测序,结果表明,突变体中OsCSLD4基因的编码区第2外显子第3 472~第3 479处有8个核苷酸(TGTGCCAC)缺失,造成移码突变,导致原编码蛋白第Ⅶ和第Ⅷ跨膜区保守功能结构域丢失,推测OsCSLD4是引起突变体zy103窄叶突变的目的基因。本研究结果为解析水稻窄叶形成的分子机理和水稻理想株型育种奠定了一定的理论基础。

关 键 词:水稻  窄叶  遗传分析  基因定位  
收稿时间:2018-01-19

Gene Identification of Narrow Leaf Mutant zy103 in Rice
YANG Yongyi,ZHOU Xuebiao,YAO Fangyin,HOU Hengjun,SUN Zhaowen,YUAN Shoujiang,ZHANG Hongrui,LI Guangxian.Gene Identification of Narrow Leaf Mutant zy103 in Rice[J].Acta Agriculturae Nucleatae Sinica,2019,33(3):421-431.
Authors:YANG Yongyi  ZHOU Xuebiao  YAO Fangyin  HOU Hengjun  SUN Zhaowen  YUAN Shoujiang  ZHANG Hongrui  LI Guangxian
Institution:1 Shandong Rice Research Institute, Jinan, Shandong 250100; 2 Shandong Center of Crop Germplasm Resources,Jinan, Shandong 250100; 3 High-tech Research Center,Shandong Academy of Agricultural Sciences, Jinan,Shandong 250100; 4 Shandong Jining Rencheng Agricultural Bureau, Jining, Shandong 272000
Abstract:Mapping and cloning of genes related to leaf morphology is essential for understanding the molecular mechanism of leaf morphogenesis. We identified a narrow leaf mutant zy103, from the F7 progeny of 9311 (Oryza sativa sup. indica)×Yujing 6 (O. sativa sup. japonica). With F2 and F3segregation populations derived from the cross between zy103 and 9311, the narrow leaf gene was finely mapped and the candidate genes were predicted. zy103 displayed narrow and semi-rolled leaves during the whole growing duration. Plant height and setting rate of zy103 were reduced, and the seeds were bended. Genetic analysis suggested that the phenotype of zy103 was controlled by one recessive nuclear gene, which was located within a 195.4 kb region on chromosome 12. There were 28 coding genes within this region. We further analyzed the candidate genes by sequencing. Eight nucleotides from 3 472 to 3 479 in the coding region of the OsCSLD4 (LOC_Os12g36890.1) gene were deleted, which caused a frameshift with concomitant loss of function the transmembrane domains of Ⅶ and Ⅷ. Therefore, OsCSLD4 is most likely to be the target gene of zy103. The results paved ways for further mechanism analysis and provided new variation for rice ideal-plant-type breeding.
Keywords:rice(Oryza sativa L  )  narrow leaf  genetic analysis  gene mapping  
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