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Identification and validation of genetic loci for tiller angle in bread wheat

机译:面包小麦耕作角度遗传基因座的识别与验证

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Key message Two major QTL for tiller angle were identified on chromosomes 1AL and 5DL, andTaTAC-D1 might be the candidate gene forQTA.caas-5DL. An ideal plant architecture is important for achieving high grain yield in crops. Tiller angle (TA) is an important factor influencing yield. In the present study, 266 recombinant inbred lines (RILs) derived from a cross between Zhongmai 871 (ZM871) and its sister line Zhongmai 895 (ZM895) was used to map TA by extreme pool-genotyping and inclusive composite interval mapping (ICIM). Two quantitative trait loci (QTL) on chromosomes 1AL and 5DL were identified with reduced tiller angle alleles contributed by ZM895.QTA.caas-1ALwas detected in six environments, explaining 5.4-11.2% of the phenotypic variances. The major stable QTL,QTA.caas-5DL, was identified in all eight environments, accounting for 13.8-24.8% of the phenotypic variances. The two QTL were further validated using BC(1)F(4)populations derived from backcrosses ZM871/ZM895//ZM871 (121 lines) and ZM871/ZM895//ZM895 (175 lines). GeneTraesCS5D02G322600, located in the 5DL QTL and designatedTaTAC-D1, had a SNP in the third exon with 'A' and 'G' in ZM871 and ZM895, respectively, resulting in aThr169Alaamino acid change. A KASP marker based on this SNP was validated in two sets of germplasm, providing further evidence for the significant effects ofTaTAC-D1on TA. Thus extreme pool-genotyping can be employed to detect QTL for plant architecture traits and KASP markers tightly linked with the QTL can be used in wheat breeding programs targeting improved plant architecture.
机译:关键消息在染色体1AL和5DL上鉴定出用于分蘖角的两个主要QTL,ANDTATAC-D1可能是候选基因FORQTA.CAAS-5DL。理想的工厂建筑对于在农作物中实现高谷产量很重要。分蘖角(TA)是影响产量的重要因素。在本研究中,使用中产871(ZM871)与其姊妹线895(ZM895)之间的266种重组近交系(RIL)通过极端池基因分型和包容性复合间隔映射来映射TA映射TA。在六种环境中检测到的ZM895.QTA.CAAS-1ALWAS贡献的减少的分蘖角等位基因,鉴定了染色体1AL和5DL的两种定量性状轨迹(QTL)。主要稳定的QTL,QTA.CAAS-5DL,在所有八种环境中都确定,占表型差异的13.8-24.8%。使用来自Backcrosses ZM871 / ZM895 // ZM871(121线)和ZM871 / ZM895 // ZM895(175行)的BC(1)F(4)群进一步验证了两个QTL。 Genetraescs5d02g322600位于5dl QTL和指定特征-D1中,分别在ZM871和ZM895中具有“A”和“G”的第三个外显子,导致AthR169Alaamino酸的变化。基于该SNP的KASP标记物在两组种质中验证,为特征-D1ON TA的显着影响提供了进一步的证据。因此,可以采用极端池基因分型来检测用于植物架构的QTL,并且与QTL紧密相关的kasp标记可用于针对改进的植物结构的小麦育种程序。

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    Chinese Acad Agr Sci CAAS Inst Crop Sci Natl Wheat Improvement Ctr 12 Zhongguancun South St Beijing 100081 Peoples R China;

    Chinese Acad Agr Sci CAAS Inst Crop Sci Natl Wheat Improvement Ctr 12 Zhongguancun South St Beijing 100081 Peoples R China;

    CAAS Inst Cotton Res 38 Huanghe Dadao Anyang 455000 Henan Peoples R China;

    Chinese Acad Agr Sci CAAS Inst Crop Sci Natl Wheat Improvement Ctr 12 Zhongguancun South St Beijing 100081 Peoples R China;

    Chinese Acad Agr Sci CAAS Inst Crop Sci Natl Wheat Improvement Ctr 12 Zhongguancun South St Beijing 100081 Peoples R China;

    CAAS Inst Cotton Res 38 Huanghe Dadao Anyang 455000 Henan Peoples R China;

    Chinese Acad Agr Sci CAAS Inst Crop Sci Natl Wheat Improvement Ctr 12 Zhongguancun South St Beijing 100081 Peoples R China;

    Chinese Acad Agr Sci CAAS Inst Crop Sci Natl Wheat Improvement Ctr 12 Zhongguancun South St Beijing 100081 Peoples R China;

    Northwest A&

    F Univ Coll Agron Yangling Shaanxi Peoples R China;

    Chinese Acad Agr Sci CAAS Inst Crop Sci Natl Wheat Improvement Ctr 12 Zhongguancun South St Beijing 100081 Peoples R China;

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  • 正文语种 eng
  • 中图分类 医学遗传学;
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