Zhang Qiuping, Liu Jiacheng, Liu Weisheng, Liu Ning, Zhang Yuping, Xu Ming, Liu Shuo, Ma Xiaoxue, Zhang Yujun
Liaoning Institute of Pomology, Yingkou, China.
Front Plant Sci. 2022 Feb 14;13:798700. doi: 10.3389/fpls.2022.798700. eCollection 2022.
Improving fruit quality is one of the main tasks in modern commercial apricot breeding. Because of the lack of high-density linkage maps and fine mapping, it is difficult to obtain molecular markers that can assist in breeding for quantitative inheritance of fruit quality traits. In this study, specific-locus amplified fragment sequencing was used to genotype 169 seedlings of F1 apricot ( L.) progenies derived from crossing "Chuanzhihong" (H) with "Saimaiti" (S). After aligning to the reference genome and filtering out low-quality variants, 6,012 high-quality single nucleotide polymorphisms were obtained and employed to construct a genetic map for each parent. The genetic linkage maps showed eight linkage groups of apricot, covering a distance of 809.6 cM in "H" and 1076.4 cM in "S". The average distance between markers in "H" and "S" was 0.62 and 0.95 cM, respectively. To map quantitative trait loci (QTLs) for fruit quality, we investigated fruit quality traits, including fruit weight (FW), fruit height (FH), fruit lateral width (FL), fruit ventral width (FV), soluble solids content (SSC), and fruit firmness (FF) for all seedlings genotyped in 2018 and 2019. Eleven and nine QTLs linked to fruit quality traits were anchored on the "H" and "S" maps, respectively, and 1,138 putative candidate genes for 16 most significant regions on the corresponding chromosome were identified based on gene annotation. Among them, fruit size contained 648 genes in 11 intervals on the reference genome, SSC contained 372 genes in 3 intervals, and FF contained 117 genes in 2 intervals. Our findings uncovered the genetic basis of apricot fruit quality, and provided candidate genes for further molecular genetic studies on fruit quality and QTL targets for future marker-assisted selection of apricot quality improvement breeding.
提高果实品质是现代商业杏育种的主要任务之一。由于缺乏高密度连锁图谱和精细定位,难以获得可辅助果实品质性状数量遗传育种的分子标记。在本研究中,利用特异性位点扩增片段测序对“串枝红”(H)与“赛买提”(S)杂交得到的169株F1代杏苗进行基因分型。将序列与参考基因组比对并过滤掉低质量变异后,获得了6012个高质量单核苷酸多态性位点,并用于构建每个亲本的遗传图谱。遗传连锁图谱显示杏有8个连锁群,在“H”图谱中覆盖距离为809.6 cM,在“S”图谱中覆盖距离为1076.4 cM。“H”和“S”图谱中标记间的平均距离分别为0.62 cM和0.95 cM。为了定位果实品质的数量性状位点(QTL),我们调查了2018年和2019年所有基因分型幼苗的果实品质性状,包括果实重量(FW)、果实高度(FH)、果实侧宽(FL)、果实腹宽(FV)、可溶性固形物含量(SSC)和果实硬度(FF)。与果实品质性状相关的11个和9个QTL分别定位在“H”和“S”图谱上,并根据基因注释确定了相应染色体上16个最显著区域的1138个推定候选基因。其中,果实大小在参考基因组上的11个区间包含648个基因,SSC在3个区间包含372个基因,FF在2个区间包含117个基因。我们的研究结果揭示了杏果实品质的遗传基础,并为进一步开展果实品质分子遗传研究提供了候选基因,以及为未来杏品质改良育种的标记辅助选择提供了QTL靶点。