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A SNP Mutation of SiCRC Regulates Seed Number Per Capsule and Capsule Length of cs1 Mutant in Sesame

机译:SiCRC的单核苷酸多态性(SNP)突变调节芝麻中每粒种子的种子数量和cs1突变体的胶囊长度。

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摘要

Seed number per capsule (SNC) is a major factor influencing seed yield and is an important trait with complex gene interaction effects. We first performed genetic analysis, gene cloning, and molecular mechanism study for an EMS-induced sesame mutant cs1 with fewer SNC and shorter capsule length (CL). The mutant traits were due to the pleiotropism of a regressive gene (Sics1). Capsule hormone determination showed that five out of 12 hormones, including auxin indole-3-acetic acid (IAA), had significantly different levels between wild type (WT) and mutant type (MT). KEGG pathway analysis showed that plant hormone signal transduction, especially the auxin signal transduction pathway, was the most abundant differentially expressed signaling pathway. After the cross-population association and regional genome screening, we found that three homozygous loci were retained in cs1. Further analysis of these three loci resulted in the identification of SiCRC as the candidate gene for cs1. SiCRC consists of seven exons and six introns encoding 163 amino acids. The SiCRC in cs1 showed a point mutation at intron 5 and exon 6 junction, resulting in the splice site being frame-shifted eight nucleotides further downstream, causing incorrect splicing. Taken together, we assumed the SNP mutation in SiCRC disrupted the function of the transcription factor, which might act downstream of the CRC-auxin signal transduction pathway, resulting in a shorter CL and less SNC mutation of cs1 in sesame. Our results highlight the molecular framework underlying the transcription factor CRC-mediated role of auxin transduction in SNC and CL development.
机译:每粒种子数(SNC)是影响种子产量的主要因素,并且是具有复杂基因相互作用效应的重要特征。我们首先对具有较少SNC和较短胶囊长度(CL)的EMS诱导的芝麻突变体cs1进行了遗传分析,基因克隆和分子机理研究。突变性状是由于回归基因的多效性(Sics1)。胶囊激素测定表明,包括生长素吲哚-3-乙酸(IAA)在内的12种激素中有5种在野生型(WT)和突变型(MT)之间具有显着不同的水平。 KEGG通路分析表明,植物激素信号转导,特别是生长素信号转导通路,是最丰富的差异表达信号通路。经过交叉种群关联和区域基因组筛选,我们发现三个纯合基因座保留在cs1中。对这三个基因座的进一步分析导致将siCRC鉴定为cs1的候选基因。 SiCRC由七个外显子和六个内含子组成,它们编码163个氨基酸。 cs1中的SiCRC在内含子5和外显子6交界处显示点突变,导致剪接位点向下游进一步移8个核苷酸,导致错误的剪接。综上所述,我们假设SiCRC中的SNP突变破坏了转录因子的功能,而后者可能在CRC-生长素信号转导途径的下游起作用,从而导致芝麻中的cs1的CL较短且SNC突变较少。我们的研究结果突出了SNC和CL发育中转录因子CRC介导的生长素转导作用的分子框架。

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