Yan Jinyuan, Zheng Bin, Wang Songbiao, Xu Wentian, Qian Minjie, Ma Xiaowei, Wu Hongxia
National Key Laboratory for Tropical Crop Breeding, Key Laboratory of Tropical Fruit Biology, Ministry of Agriculture and Rural Affairs, Key Laboratory of Hainan Province for Postharvest Physiology and Technology of Tropical Horticulture Products, South Subtropical Crops Research Institute, Chinese Academy of Tropical Agricultural Sciences, Zhanjiang 524013, China.
Sanya Research Institute, Chinese Academy of Tropical Agricultural Sciences, Sanya 572024, China.
Int J Mol Sci. 2024 Dec 19;25(24):13625. doi: 10.3390/ijms252413625.
Mango ( L.) (2n = 40) is an important perennial fruit tree in tropical and subtropical regions. The lack of information on genetic diversity at the molecular level hinders efforts in mango genetic improvement and molecular marker-assisted breeding. In this study, a genome-wide screening was conducted to develop simple sequence repeat (SSR) markers using the Alphonso reference genome. A total of 187 SSR primer pairs were designed based on SSR loci with consisting of tri- to hexa-nucleotide motifs, and 34 highly polymorphic primer pairs were selected to analyze the diversity of 231 germplasm resources. These primers amplified 219 alleles () across 231 accessions, averaging of 6.441 alleles for per marker. The polymorphic information content (PIC) values ranged from 0.509 to 0.757 with a mean of 0.620. Genetic diversity varied among populations, with Southeast Asia showing the highest diversity, and Australia the lowest. Population structure analysis, divided the accessions into two groups, Group I (India) and Group II (Southeast Asia), containing 104 and 127 accessions, respectively, consistent with results from phylogenetic analysis and principal component analysis (PCA). Sixteen SSR primer pairs capable of distinguishing all tested accessions, were selected as core primers for constructing fingerprints of 229 mango accessions. These findings offer valuable resources for enhancing the utilization of mango germplasm in breeding programs.
芒果(Mangifera indica L.)(2n = 40)是热带和亚热带地区一种重要的多年生果树。分子水平上遗传多样性信息的缺乏阻碍了芒果遗传改良和分子标记辅助育种工作。在本研究中,利用阿方索芒果参考基因组进行了全基因组筛选以开发简单序列重复(SSR)标记。基于由三到六核苷酸基序组成的SSR位点共设计了187对SSR引物对,并选择了34对高度多态性引物对来分析231份种质资源的多样性。这些引物在231份材料中扩增出219个等位基因,每个标记平均有6.441个等位基因。多态信息含量(PIC)值范围为0.509至0.757,平均值为0.620。不同群体间遗传多样性存在差异,东南亚地区多样性最高,澳大利亚最低。群体结构分析将这些材料分为两组,第一组(印度)和第二组(东南亚),分别包含104份和127份材料,这与系统发育分析和主成分分析(PCA)的结果一致。选择16对能够区分所有测试材料的SSR引物对作为构建229份芒果材料指纹图谱的核心引物。这些研究结果为提高芒果种质在育种计划中的利用提供了宝贵资源。