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水稻显性脆秆突变体Bc18的鉴定和基因定位
引用本文:彭应财,刘文真,傅亚萍,王鹤潼,胡国成,陈温福,徐正进.水稻显性脆秆突变体Bc18的鉴定和基因定位[J].中国水稻科学,2016,30(2):127-135.
作者姓名:彭应财  刘文真  傅亚萍  王鹤潼  胡国成  陈温福  徐正进
作者单位:1.沈阳农业大学 农学院, 沈阳 110866;2.中国水稻研究所, 杭州 310006
基金项目:中央级科研院所基本科研业务费专项(2014RG001-5);中国农业科学院超级稻杂种优势机理研究创新团队资助项目(CAAS-ASTIP-2013-CNRRI)
摘    要:从三交组合Ⅱ-32B//协青早B/Dular的F2群体中获得了1个脆性突变体,整个植株表现全生育期脆性。根据该突变体的表型,将其命名为Bc18(Brittle culm 18)。为了更好地鉴定该突变体,用正常茎秆强度品种中9B作轮回亲本与Bc18杂交,创制了Bc18脆秆近等基因系中脆B和中9B。表型鉴定显示,突变体Bc18在生育期、株高、单株穗数、每穗粒数、结实率和千粒重等主要农艺和产量性状上与野生型中9B 无显著差别,但茎、叶的机械强度分别下降了70.70%和47.16%。细胞壁组分分析表明,突变体Bc18茎、叶的纤维素和木质素含量与野生型中9B 无显著差异,但半纤维素含量分别提高了31.84%和17.35%。6个杂交组合F2和12个回交BC1F1群体的遗传分析证明Bc18 脆性突变由单显性基因控制。采用图位克隆技术,构建了Bc18/02428和Bc18/9311的F2定位群体,并利用网上公布的SSR标记和新设计的InDel标记,最终将Bc18基因定位在第1染色体长臂端InDel标记PBC22与PBC33之间约154 kb的区间内。

关 键 词:水稻  Bc18  显性脆秆  机械强度  半纤维素含量  基因定位  
收稿时间:2015-11-02
修稿时间:2015-11-22

Characterization and Gene Mapping of a Dominant Brittle Culm Mutant Bc18 in Rice (Oryza sativa L.)
Ying-cai PENG,Wen-zhen LIU,Ya-ping FU,He-tong WANG,Guo-cheng HU,Wen-fu CHEN,Zheng-jin XU.Characterization and Gene Mapping of a Dominant Brittle Culm Mutant Bc18 in Rice (Oryza sativa L.)[J].Chinese Journal of Rice Science,2016,30(2):127-135.
Authors:Ying-cai PENG  Wen-zhen LIU  Ya-ping FU  He-tong WANG  Guo-cheng HU  Wen-fu CHEN  Zheng-jin XU
Institution:1. College of Agronomy, Shenyang Agricultural University, Shenyang 110866, China;2.China National Rice Research Institue, Hangzhou 310006, China
Abstract:A brittle culm mutant was obtained from the F2 population of three-way cross Ⅱ-32B//Xieqingzao B/Dular and named as Brittle culm 18 ( Bc18 ) according to its phenotypes. Each part of plant showed brittleness during the whole growth period. In order to identify the mutant, near isogenic line populations of Zhongcui B and Zhong 9B were created with Bc18 mutant as the donor of brittle gene and Zhong 9B, a normal culm-strength variety, as the receptor and recurrent parent. Compared with wild type, Bc18 significantly declined by 70.70% and 47.16% in mechanical strength of culm and leaves, respectively. No significant differences were found in terms of growth duration, plant height, panicle number per plant, spikelet number per panicle, seed setting rate and 1000-grain weight. Cell wall components analyses showed that cellulose content and lignin content in Bc18 had no significant difference as compared with those of wild type, while hemicellulose content in culm and leaf dramatically increased by 31.84% and 17.35%, respectively. Genetic analyses of six F2 and twelve BC1F1 backcross populations revealed that the phenotype of Bc18 was controlled by a single dominant gene. Bc18/02428 and Bc18/9311 F2 populations were developed for Bc18 gene mapping. By means of map-based cloning technology, with some SSR markers published online and new designed InDel markers, Bc18 was localized between InDel marker PBC22 and PBC33 at a physical distance of about 154 kb on the long arm of chromosome 1. This work laid the foundation for cloning Bc18 gene in the future.
Keywords:rice ( Oryza sativa L  )  Bc18  dominant brittle culm  mechanical strength  hemicellulose content  gene mapping  
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