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QTL Analysis of Head Splitting Resistance in Cabbage (Brassica oleracea L. var. capitata) Using SSR and InDel Makers Based on Whole-Genome Re-Sequencing

机译:基于全基因组重新测序的SSR和InDel标记分析白菜头部抗裂性的QTL分析

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摘要

Head splitting resistance (HSR) in cabbage is an important trait closely related to both quality and yield of head. However, the genetic control of this trait remains unclear. In this study, a doubled haploid (DH) population derived from an intra-cross between head splitting-susceptible inbred cabbage line 79–156 and resistant line 96–100 was obtained and used to analyze inheritance and detect quantitative trait loci (QTLs) for HSR using a mixed major gene/polygene inheritance analysis and QTL mapping. HSR can be attributed to additive-epistatic effects of three major gene pairs combined with those of polygenes. Negative and significant correlations were also detected between head Hsr and head vertical diameter (Hvd), head transverse diameter (Htd) and head weight (Hw). Using the DH population, a genetic map was constructed with simple sequence repeat (SSR) and insertion–deletion (InDel) markers, with a total length of 1065.9 cM and average interval length of 4.4 cM between adjacent markers. Nine QTLs for HSR were located on chromosomes C3, C4, C7, and C9 based on 2 years of phenotypic data using both multiple-QTL mapping and inclusive composite interval mapping. The identified QTLs collectively explained 39.4 to 59.1% of phenotypic variation. Three major QTLs (Hsr 3.2, 4.2, 9.2) showing a relatively larger effect were robustly detected in different years or with different mapping methods. The HSR trait was shown to have complex genetic mechanisms. Results from QTL mapping and classical genetic analysis were consistent. The QTLs obtained in this study should be useful for molecular marker-assisted selection in cabbage breeding and provide a foundation for further research on HSR genetic regulation.
机译:卷心菜的抗头裂性(HSR)是与头的质量和产量密切相关的重要性状。但是,该性状的遗传控制仍不清楚。在这项研究中,获得了从头裂易感近交甘蓝自交系79-156和抗性自交系96-100之间杂交获得的双倍单倍体(DH)种群,并用于分析遗传和检测QTLs HSR使用主要基因/多基因混合遗传分析和QTL定位。 HSR可以归因于三个主要基因对与多基因相结合的累加上位效应。头部Hsr与头部垂直直径(Hvd),头部横向直径(Htd)和头部重量(Hw)之间也检测到负相关和显着相关性。利用DH群体,构建了具有简单序列重复(SSR)和插入缺失(InDel)标记的遗传图谱,总长度为1065.9 cM,相邻标记之间的平均间隔长度为4.4 cM。基于两年的表型数据,使用多重QTL定位和包含性复合区间定位的9个HSR QTL位于染色体C3,C4,C7和C9上。鉴定出的QTL共同解释了表型变异的39.4%至59.1%。在不同年份或使用不同的制图方法,均能可靠地检测到显示出较大影响的三个主要QTL(Hsr 3.2、4.2、9.2)。高铁性状显示出具有复杂的遗传机制。 QTL作图和经典遗传分析的结果是一致的。本研究中获得的QTLs可用于甘蓝育种中分子标记辅助选择,并为进一步研究高铁遗传调控提供基础。

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