机构地区:[1]江西农业大学林学院,南昌330045 [2]江西农业大学猕猴桃研究所,南昌330045
出 处:《果树学报》2018年第6期658-667,共10页Journal of Fruit Science
基 金:国家自然科学基金(31760559;31760567;31460505);江西省重大科技专项(20161ACF60007);江西省现代农业产业技术体系建设专项(JXARS-05)
摘 要:【目的】研究江西省内野生毛花猕猴桃雄性种质的多样性。【方法】对江西省野生毛花猕猴桃雄性种质资源开展调查和收集,分析花器表型性状变异和SSR遗传多样性。【结果】供试68份毛花猕猴桃雄性种质的雄花花器在表型性状和DNA分子水平上均存在明显的变异和较丰富的遗传多样性,表型性状平均变异系数为29.19%,其中变异幅度最大的为花粉量(53.41%),最小的为花冠直径(15.47%)。通过表型聚类分析,可将该68份种质资源分为两大类群,类群A可分为2个亚类,大部分样品聚为第1亚类,主要表现为花梗较短,花冠较大,花粉活力较高,花冠颜色为粉红;第2亚类总体表现为花梗较长,花冠较小,花粉活力中等。类群B仅有2份样品,其特征为花冠大、雄蕊数多和高花粉量,在DNA分子水平上,筛选到的15对SSR有效引物共扩增出87个等位位点,均为多态性位点。Shannon’s信息指数为1.04,多态信息含量为46.48%。UPGMA聚类分析可将供试种质材料分为3类。2种聚类结果相似,Mantel分析中表型性状与分子标记结果呈显著相关(r=-0.79,p<0.05),SSR分子标记在一定程度上反映了不同毛花猕猴桃雄性种质表型性状的变异情况。【结论】68份野生毛花猕猴桃雄性种质表现出较丰富的遗传多样性。其中花粉量、单花雄蕊数、花粉活力、花瓣颜色、花丝颜色、花梗长度是造成表型性状差异的主要因素。SSR分子标记分析与毛花猕猴桃花器表型聚类结果具有显著相关性,毛花猕猴桃雄花的多种表型性状是环境和基因共同作用的结果。【Objective】Kiwifruit(Actinidia Lindl.) has gotten a short history of domestication since the early 20 th century when its seeds were introduced into New Zealand. It is wildly distributed throughout the most area of East Asia. The center for the origin of kiwifruit has been considered to be the mountains of the Southwestern China. Jiangxi province is one of the distribution areas of the kiwifruit. Actinidia eriantha Benth. is recognized as a valuable species for commercial kiwifruit improvement for high content of ascorbic acid as well as being used in traditional Chinese medicine. Molecular studies have been proved to be efficient ways for the survey of fruit germplasms. The objective of this study was toassess male A. eriantha genetic diversity and to determine the differences among 68 germplasms grown in Jiangxi province by examining both morphological and molecular characteristics.【Methods】We conducted a simple sequence repeat(SSR)-based analysis of 68 germplasms from 7 regions of Jiangxi province. We also conducted morphological trait association analysis with 10 important floral phenotypic characteristics and 87 SSR loci. The morphological traits were recorded based on the Guidelines for the conduct of tests for distinctness, uniformity, and stability: kiwifruit(Actinidia L.). 50 SSR pairs of primers even distributed on the genetic linkage map of A. chinensis were used to initially assess the polymorphism. Of the 50 pairs of primers tested, 15 pairs successfully amplified polymorphic fragments. The phenotypic variables were analyzed using software SPSS. SSR analysis was carried out using fifteen pairs of primers. NTSYSpc2.1 was used for estimating the level of genetic diversity according to the SSR data. The polymorphism information content(PIC) and the Shannon's information index for each SSR were calculated for measuring the informativeness of the markers. The relationship between the Euclidean distances measured using phenotypic variables and the distances measured using SSR ma
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