首页|甜瓜控制单果重基因的精细定位及候选基因分析

甜瓜控制单果重基因的精细定位及候选基因分析

扫码查看
轻果型材料1244(单果重22.59 g)和重果型材料MS-5(单果重 814.97 g)配置杂交组合后获得F2∶3 分离群体,采用插入缺失(InDel)标记对控制单果重性状的主效QTL位点sfw2.2进行精细定位,进一步对定位区间内的注释基因进行分析,以确定关键候选基因.结果表明:控制单果重性状的主效QTL位点sfw2.2 定位在标记CY InDel11 和CY InDel16 之间,包含 3个已知功能基因.其中,纤维蛋白合成相关基因MELO3C029669 的相对表达量在两个亲本间存在显著差异,推测其为控制甜瓜单果重的关键基因.根据基因在亲本间的序列差异,开发特异性InDel分子标记BCYInDel13 对 30 份甜瓜材料苗期进行单果重性状的检测,检测准确率可达到 90%,具有较高的准确性.
Fine Mapping and Candidate Gene Analysis of Single Fruit Weight Gene in Melon
The light fruit type melon 1244(single fruit weight 22.59 g)was crossed with the heavy fruit type melon MS-5(single fruit weight 814.97 g)and the segregation population F2∶3 was obtained.Insertion-deletion(InDel)marker were used for fine mapping of a major QTL locus sfw2.2,which control single fruit weight,and the annotated genes in the mapping region were further analyzed to identify candidate target gene.Results showed,a major QTL locus sfw2.2 of single fruit weight was delimited between markers CY InDel11and CY InDel16,in which contained three known functional genes.Among of them,the relative expression of MELO3C029669 gene,which was fibrin synthesis-related gene,showed significant difference between two parents,suggesting that MELO3C029669 may be a candidate gene for controlling single fruit weight of melon.According to the gene structure differences between two parents of MELO3C029669,specific InDel molecular marker BCYInDel was designed to detect the signal fruit weight trait of 30 melon materials,and accuracy of results reached high accuracy 90.0%.

melonsingle fruit weightInDel markerqRT-PCR

萨日娜、才羿、王新宇、李子尚、于迪、姚琼、孙雪雯、卢欣欣、盛云燕

展开 >

黑龙江八一农垦大学园艺园林学院,大庆 163319

黑龙江省农业科学院园艺分院

甜瓜 单果重 InDel标记 qRT-PCR

黑龙江八一农垦大学博士启动基金黑龙江省自然科学基金联合基金

XYB202116LH2022C065

2024

黑龙江八一农垦大学学报
黑龙江八一农垦大学

黑龙江八一农垦大学学报

影响因子:0.888
ISSN:1002-2090
年,卷(期):2024.36(2)
  • 24