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QTL-Seq Identified a Major QTL for Grain Length and Weight in Rice Using Near Isogenic F2Population

机译:QTL-Seq使用近等基因F2群体鉴定了水稻籽粒长度和重量的主要QTL

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摘要

Mapping and isolation of quantitative trait loci (QTLs) or genes controlling grain size or weight is very important to uncover the molecular mechanisms of seed development and crop breeding. To identify the QTLs controlling grain size and weight, we developed a near isogenic line F2(NIL-F2) population, which was derived from a residual heterozygous plant in an F7generation of recombinant inbred line (RIL). With the completion of more than 30× whole genome re-sequencing of the parents, two DNA bulks for large and small grains, a total of 58.94 Gb clean nucleotide data were generated. A total of 455 262 single nucleotide polymorphisms (SNPs) between the parents were identified to perform bulked QTL-seq. A candidate genomic region containing SNPs strongly associated with grain length and weight was identified from 15 to 20 Mb on chromosome 5. We designated the major QTL in the candidate region as qTGW5.3.Then,qTGW5.3 was further validated with PCR-based conventional QTL mapping method through developing simple sequence repeat and Insertion/Deletion markers in the F2population. Furthermore,recombinants and the progeny tests delimited the candidate region of qTGW5.3 to 1.13 Mb, flanked by HX5009 (15.15 Mb) and HX5003 (16.28 Mb). A set of NILs, selected from the F2population, was developed to evaluate the genetic effect of qTGW5.3.Significant QTL effects were detected on grain length, grain width and 1000-grain weight of H12-29 allele with 1.14 mm, -0.11 mm and 3.11 g, which explained 99.64%, 95.51% and 97.32% of the phenotypic variations, respectively.
机译:定位和分离数量性状基因座(QTL)或控制晶粒大小或重量的基因对于揭示种子发育和农作物育种的分子机制非常重要。为了确定控制晶粒大小和重量的QTL,我们开发了近等基因系F2(NIL-F2)种群,该种群来自重组近交系(RIL)的F7代中的残留杂合植物。亲本完成了超过30倍的全基因组重测序,生成了两个大大小小的DNA块,共产生了58.94 Gb的纯净核苷酸数据。亲本之间的总共455 262个单核苷酸多态性(SNP)被鉴定为执行大量QTL-seq。在5号染色体上从15到20 Mb鉴定了一个与SNPs高度相关的候选基因组区域。我们将候选区域中的主要QTL命名为qTGW5.3。然后,基于PCR的方法进一步验证了qTGW5.3通过在F2种群中开发简单的序列重复序列和插入/缺失标记来实现传统的QTL定位方法。此外,重组子和后代测试将qTGW5.3的候选区域限定为1.13 Mb,两侧是HX5009(15.15 Mb)和HX5003(16.28 Mb)。开发了一组从F2种群中选出的NIL来评估qTGW5.3的遗传效应。检测到显着QTL效应对1.12 mm -0.11 mm的H12-29等位基因的粒长,粒宽和1000粒重的影响和3.11 g,分别解释了99.64%,95.51%和97.32%的表型变异。

著录项

  • 来源
    《水稻科学(英文版)》 |2018年第3期|121-131|共11页
  • 作者单位

    State Key Laboratory of Rice Biology/Chinese National Center for Rice Improvement, China National Rice Research Institute, Hangzhou 310006, China;

    Key Laboratory of Plant Molecular Physiology/Institute of Botany, the Chinese Academy of Sciences, Beijing 100093, China;

    State Key Laboratory of Rice Biology/Chinese National Center for Rice Improvement, China National Rice Research Institute, Hangzhou 310006, China;

    State Key Laboratory of Rice Biology/Chinese National Center for Rice Improvement, China National Rice Research Institute, Hangzhou 310006, China;

    State Key Laboratory of Rice Biology/Chinese National Center for Rice Improvement, China National Rice Research Institute, Hangzhou 310006, China;

    Institute of Rice Research, Fujian Academy of Agricultural Sciences/Fuzhou National Sub-Center for Rice Improvement, Fuzhou 350018, China;

    Key Laboratory of Plant Molecular Physiology/Institute of Botany, the Chinese Academy of Sciences, Beijing 100093, China;

    State Key Laboratory of Rice Biology/Chinese National Center for Rice Improvement, China National Rice Research Institute, Hangzhou 310006, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-19 04:05:57
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