首页> 外文期刊>Scientific reports. >High-density linkage map construction and mapping of seed trait QTLs in chickpea (Cicer arietinum L.) using Genotyping-by-Sequencing (GBS)
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High-density linkage map construction and mapping of seed trait QTLs in chickpea (Cicer arietinum L.) using Genotyping-by-Sequencing (GBS)

机译:使用基因分型逐序列(GBS),高密度连杆地图结构和种子性状QTLs的曲线( Cicer Arietinum L.)

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This study reports the use of Genotyping-by-Sequencing (GBS) for large-scale SNP discovery and simultaneous genotyping of recombinant inbred lines (RILs) of an intra-specific mapping population of chickpea contrasting for seed traits. A total of 119,672 raw SNPs were discovered, which after stringent filtering revealed 3,977 high quality SNPs of which 39.5% were present in genic regions. Comparative analysis using physically mapped marker loci revealed a higher degree of synteny with Medicago in comparison to soybean. The SNP genotyping data was utilized to construct one of the most saturated intra-specific genetic linkage maps of chickpea having 3,363 mapped positions including 3,228 SNPs on 8 linkage groups spanning 1006.98?cM at an average inter marker distance of 0.33?cM. The map was utilized to identify 20 quantitative trait loci (QTLs) associated with seed traits accounting for phenotypic variations ranging from 9.97% to 29.71%. Analysis of the genomic sequence corresponding to five robust QTLs led to the identification of 684 putative candidate genes whose expression profiling revealed that 101 genes exhibited seed specific expression. The integrated approach utilizing the identified QTLs along with the available genome and transcriptome could serve as a platform for candidate gene identification for molecular breeding of chickpea.
机译:本研究报告了使用基因分型逐序列(GBS)用于大规模的SNP发现和同时进行鸡眼的特异性测绘群的重组近交系(RIL)对种子性状的对比。发现总共119,672个未加工的SNP,其严格滤波显示3,977个高质量的SNP,其中遗传区域存在39.5%。与大豆相比,使用物理映射标记基因座的比较分析显示了Medicago的更高程度的同时性。 SNP基因分型数据用于构建具有3,363个映射位置的鸡眼的最饱和的特异性遗传联系地图中的一种,包括3,228个SNP,跨越1006.98Ωcm的平均标记距离为0.33Ωcm。使用该地图鉴定与种子特征相关的20个定量性状基因座(QTLS),核算从9.97%到29.71%的表型变化。对应于五个稳健QTL的基因组序列的分析导致了684个候选候选基因的鉴定,其表达分析显示101基因表现出种子特异性表达。利用所识别的QTL和可用基因组和转录组的综合方法可以作为鸡豆分子育种的候选基因鉴定的平台。

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