School of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong, Shaanxi Province, China.
Shaanxi Province Key Laboratory of Bio-resources, Hanzhong, Shaanxi Province, China.
Hereditas. 2024 May 17;161(1):18. doi: 10.1186/s41065-024-00321-3.
Kiwifruit (Actinidiaceae family) is an economically important fruit tree in China and New Zealand. It is a typical dioecious plant that has undergone frequent natural hybridization, along with chromosomal ploidy diversity within the genus Actinidia, resulting in higher genetic differences and horticultural diversity between interspecific and intraspecific traits. This diversity provides a rich genetic base for breeding. China is not only the original center of speciation for the Actinidia genus but also its distribution center, housing the most domesticated species: A. chinensis var. chinensis, A. chinensis var. deliciosa, A. arguta, and A. polygama. However, there have been relatively few studies on the application of DNA markers and the genetic basis of kiwifruit plants. By combining information from chloroplast-specific SNPs and nuclear SCoT (nSCoT) markers, we can uncover complementary aspects of genetic variation, population structure, and evolutionary relationships. In this study, one chloroplast DNA (cpDNA) marker pair was selected out of nine cpDNA candidate pairs. Twenty nSCoT markers were selected and used to assess the population structure and chloroplast-specific DNA haplotype diversity in 55 kiwifruit plants (Actinidia), including 20 samples of A. chinensis var. chinensis, 22 samples of A. chinensis var. deliciosa, 11 samples of A. arguta, and two samples of A. polygama, based on morphological observations collected from China.
The average genetic distance among the 55 samples was 0.26 with chloroplast-specific SNP markers and 0.57 with nSCoT markers. The Mantel test revealed a very small correlation (r = 0.21). The 55 samples were categorized into different sub-populations using Bayesian analysis, the Unweighted Pair Group Method with the Arithmetic Mean (UPGMA), and the Principal Component Analysis (PCA) method, respectively. Based on the analysis of 205 variable sites, a total of 15 chloroplast-specific DNA haplotypes were observed, contributing to a higher level of polymorphism with an Hd of 0.78. Most of the chloroplast-specific DNA haplotype diversity was distributed among populations, but significant diversity was also observed within populations. H1 was shared by 24 samples, including 12 of A. chinensis var. chinensis and 12 of A. chinensis var. deliciosa, indicating that H1 is an ancient and dominant haplotype among the 55 chloroplast-specific sequences. H2 may not have evolved further.The remaining haplotypes were rare and unique, with some appearing to be exclusive to a particular variety and often detected in single individuals. For example, the H15 haplotype was found exclusively in A. polygama.
The population genetic variation explained by chloroplast-specific SNP markers has greater power than that explained by nSCoTs, with chloroplast-specific DNA haplotypes being the most efficient. Gene flow appears to be more evident between A. chinensis var. chinensis and A. chinensis var. deliciosa, as they share chloroplast-specific DNA haplotypes, In contrast, A.arguta and A. polygama possess their own characteristic haplotypes, derived from the haplotype of A. chinensis var. chinensis. Compared with A. chinensis, the A.arguta and A. polygama showed better grouping. It also seems crucial to screen out, for each type of molecular marker, especially haplotypes, the core markers of the Actinidia genus.
猕猴桃(猕猴桃科)是中国和新西兰的一种重要经济水果树。它是一种典型的雌雄异株植物,经历了频繁的自然杂交,以及猕猴桃属内的染色体多倍体多样性,导致种间和种内性状之间的遗传差异和园艺多样性更高。这种多样性为育种提供了丰富的遗传基础。中国不仅是猕猴桃属的物种形成的原始中心,也是其分布中心,拥有最驯化的物种:中华猕猴桃、美味猕猴桃、软枣猕猴桃和狗枣猕猴桃。然而,关于猕猴桃植物的 DNA 标记应用和遗传基础的研究相对较少。通过结合叶绿体特异性 SNP 和核 SCoT(nSCoT)标记的信息,可以揭示遗传变异、种群结构和进化关系的互补方面。在这项研究中,从九个叶绿体候选对中选择了一对叶绿体 DNA(cpDNA)标记。选择了 20 个 nSCoT 标记,用于评估来自中国的 55 株猕猴桃植物(猕猴桃属)的种群结构和叶绿体特异性 DNA 单倍型多样性,包括 20 个中华猕猴桃样本、22 个美味猕猴桃样本、11 个软枣猕猴桃样本和 2 个狗枣猕猴桃样本。
55 个样本的平均遗传距离分别为 0.26 和 0.57 用叶绿体特异性 SNP 标记和 nSCoT 标记。Mantel 检验显示相关性非常小(r=0.21)。贝叶斯分析、非加权对组平均法(UPGMA)和主成分分析(PCA)方法分别将 55 个样本分为不同的亚群。基于 205 个可变位点的分析,共观察到 15 种叶绿体特异性 DNA 单倍型,具有较高的多态性,Hd 为 0.78。大多数叶绿体特异性 DNA 单倍型多样性分布在种群之间,但也观察到种群内的显著多样性。H1 被 24 个样本共享,包括 12 个中华猕猴桃和 12 个美味猕猴桃,表明 H1 是 55 个叶绿体特异性序列中的一个古老且占主导地位的单倍型。H2 可能没有进一步进化。其余的单倍型是罕见和独特的,有些单倍型似乎是特定品种所独有的,并且经常在单个个体中检测到。例如,H15 单倍型仅在狗枣猕猴桃中发现。
叶绿体特异性 SNP 标记解释的种群遗传变异比 nSCoT 标记解释的具有更大的功效,叶绿体特异性 DNA 单倍型是最有效的。基因流似乎在中华猕猴桃和美味猕猴桃之间更为明显,因为它们共享叶绿体特异性 DNA 单倍型,而软枣猕猴桃和狗枣猕猴桃则具有自己的特征单倍型,源自中华猕猴桃的单倍型。与中华猕猴桃相比,软枣猕猴桃和狗枣猕猴桃的分组情况更好。对于每种类型的分子标记,特别是单倍型,筛选猕猴桃属的核心标记似乎也很重要。