Guo Rui, Landis Jacob B, Moore Michael J, Meng Aiping, Jian Shuguang, Yao Xiaohong, Wang Hengchang
Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Chinese Academy of SciencesWuhan, China.
College of Life Sciences, University of Chinese Academy of SciencesBeijing, China.
Front Plant Sci. 2017 Aug 25;8:1383. doi: 10.3389/fpls.2017.01383. eCollection 2017.
Benth. is a diploid perennial woody vine native to China and is recognized as a valuable species for commercial kiwifruit improvement with high levels of ascorbic acid as well as having been used in traditional Chinese medicine. Due to the lack of genomic resources for the species, microsatellite markers for population genetics studies are scarce. In this study, RNASeq was conducted on fruit tissue of , yielding 5,678,129 reads with a total output of 3.41 Gb. assembly yielded 69,783 non-redundant unigenes (41.3 Mb), of which 21,730 were annotated using protein databases. A total of 8,658 EST-SSR loci were identified in 7,495 unigene sequences, for which primer pairs were successfully designed for 3,842 loci (44.4%). Among these, 183 primer pairs were assayed for PCR amplification, yielding 69 with detectable polymorphism in . Additionally, 61 of the 69 polymorphic loci could be successfully amplified in at least one other species. Of these, 14 polymorphic loci (mean = 6.07 ± 2.30) were randomly selected for assessing levels of genetic diversity and population structure within . Finally, a neighbor-joining tree and Bayesian clustering analysis showed distinct clustering into two groups ( = 2), agreeing with the geographical distributions of these populations. Overall, our results will facilitate further studies of genetic diversity within and will aid in discriminating outlier loci involved in local adaptation.
本氏猕猴桃是一种二倍体多年生木本藤本植物,原产于中国,因其富含高水平的抗坏血酸而被认为是用于商业猕猴桃改良的珍贵物种,并且已被用于传统中药。由于该物种缺乏基因组资源,用于群体遗传学研究的微卫星标记很少。在本研究中,对本氏猕猴桃的果实组织进行了RNA测序,产生了5,678,129条读数,总输出量为3.41 Gb。组装产生了69,783个非冗余单基因(41.3 Mb),其中21,730个使用蛋白质数据库进行了注释。在7,495个单基因序列中总共鉴定出8,658个EST-SSR位点,成功为其中3,842个位点(44.4%)设计了引物对。其中,对183对引物进行了PCR扩增检测,在本氏猕猴桃中产生了69个具有可检测多态性的引物。此外,69个多态性位点中的61个可以在至少一种其他猕猴桃物种中成功扩增。其中,随机选择了14个多态性位点(平均 = 6.07 ± 2.30)来评估本氏猕猴桃内的遗传多样性水平和群体结构。最后,邻接法树和贝叶斯聚类分析显示明显聚为两组(K = 2),与这些群体的地理分布一致。总体而言,我们的结果将有助于进一步研究本氏猕猴桃内的遗传多样性,并有助于识别参与局部适应的异常位点。