首页> 外文期刊>BMC Plant Biology >Identification of a SiCL1 gene controlling leaf curling and capsule indehiscence in sesame via cross-population association mapping and genomic variants screening
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Identification of a SiCL1 gene controlling leaf curling and capsule indehiscence in sesame via cross-population association mapping and genomic variants screening

机译:通过交叉种群关联作图和基因组变异筛选鉴定控制芝麻卷曲和胶囊开裂的SiCL1基因

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Leaf shape can affect plantlet development and seed yield in sesame. The morphological, histological and genetic analyses of a sesame mutant cl1 (cl) with curly leaf and indehiscent capsule traits were performed in this study. In order to clone the cl1 gene for breeding selection, genome re-sequencing of the 130 individuals of cl1?×?USA (0)-26?F2 population and a bulked segregation analysis (BSA) pool was carried out. The genome re-sequencing data of the 822 germplasm with normal leaf shape were applied. For cl1 mutant, the adaxial/abaxial character of the parenchyma cells in the leaf blades is reduced. Results proved that the leaf curling trait is controlled by a recessive gene (Sicl1). Cross- population association of the F2 population of cl1?×?USA (0)-26 indicated that the target cl locus was located on the interval C29 between C29_6522236 and C29_6918901 of SiChr. 1. Further regional genome variants screening determined the 6 candidate variants using genomic variants data of 822 natural germplasm and a BSA pool data. Of which, 5 markers C29_6717525, C29_6721553, C29_6721558, C29_6721563, and C29_6721565 existed in the same gene (C29.460). With the aid of the validation in the test F2 population of cl1?×?Yuzhi 11 and natural germplasm, the integrated marker SiCLInDel1 (C29: 6721553–6721572) was determined as the target marker, and C29.460 was the target gene SiCL1 in sesame. SiCL1 is a KAN1 homolog with the full length of 6835?bp. In cl1, the 20 nucleic acids (CAGGTAGCTATGTATATGCA) of SiCLInDel1 marker were mutagenized into 6 nucleic acids (TCTTTG). The deletion led to a frameshift mutation and resulted in the earlier translation termination of the CL gene. The Sicl1 allele was shortened to 1829?bp. SiCL1 gene was expressed mainly in the tissues of stem, leaf, bud, capsule and seed. SiCL1 encodes a transcription repressor KAN1 protein and controls leaf curling and capsule indehiscence in sesame. The findings provided an example of high-efficient gene cloning in sesame. The SiCL1 gene and the cl1 mutant supply the opportunity to explore the development regulation of leaf and capsule, and would improve the new variety breeding with high harvest mechanization adaption in sesame.
机译:叶片形状会影响芝麻的幼苗生长和种子产量。在这项研究中进行了芝麻叶片卷曲和不裂性状的cl1(cl)的形态,组织学和遗传学分析。为了克隆cl1基因用于选育,对cl1××USA(0)-26ΔF2群体的130个个体进行了基因组重测序,并进行了大块分离分析(BSA)库。应用了具有正常叶片形状的822种质的基因组重测序数据。对于cl1突变体,叶片中薄壁细胞的近轴/近轴特性降低。结果证明,叶片的卷曲特性受隐性基因(Sicl1)控制。 cl1?x?USA(0)-26的F2种群的跨种群关联表明目标cl基因座位于SiChr的C29_6522236和C29_6918901之间的区间C29上。 1.进一步的区域基因组变异筛选使用822个天然种质的基因组变异数据和BSA库数据确定了6个候选变异。其中,同一基因(C29.460)中存在5个标记C29_6717525,C29_6721553,C29_6721558,C29_6721563和C29_6721565。借助于在测试F2群体中的cl1?×?Yuzhi 11和天然种质的验证,确定了整合标记SiCLInDel1(C29:6721553–6721572)作为目标标记,而C29.460是目标基因SiCL1。芝麻。 SiCL1是一个KAN1同源物,全长6835?bp。在cl1中,将SiCLInDel1标记的20个核酸(CAGGTAGCTATGTATATGCA)诱变为6个核酸(TCTTTG)。该删除导致移码突变,并导致CL基因的更早翻译终止。 Sicl1等位基因缩短为1829?bp。 SiCL1基因主要在茎,叶,芽,荚膜和种子的组织中表达。 SiCL1编码转录阻遏物KAN1蛋白,并控制芝麻中的叶子卷曲和胶囊开裂。该发现提供了芝麻中高效基因克隆的实例。 SiCL1基因和cl1突变体为探索叶片和荚膜的发育规律提供了机会,并通过芝麻的高收获机械化适应性改良了新品种的选育。

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