Li Xiaobai, Jin Feng, Jin Liang, Jackson Aaron, Huang Cheng, Li Kehu, Shu Xiaoli
Zhejiang Academy of Agricultural Sciences, Shiqiao Road 139, Hangzhou, 310021, People's Republic of China.
Hubei University, College of Life Sciences, Wuhan, 430062, People's Republic of China.
BMC Genet. 2014 Dec 5;15:124. doi: 10.1186/s12863-014-0124-5.
Cymbidium is a genus of 68 species in the orchid family, with extremely high ornamental value. Marker-assisted selection has proven to be an effective strategy in accelerating plant breeding for many plant species. Analysis of cymbidiums genetic background by molecular markers can be of great value in assisting parental selection and breeding strategy design, however, in plants such as cymbidiums limited genomic resources exist. In order to obtain efficient markers, we deep sequenced the C. ensifolium transcriptome to identify simple sequence repeats derived from gene regions (genic-SSR).
The 7,936 genic-SSR markers were identified. A total of 80 genic-SSRs were selected, and primers were designed according to their flanking sequences. Of the 80 genic-SSR primer sets, 62 were amplified in C. ensifolium successfully, and 55 showed polymorphism when cross-tested among 9 Cymbidium species comprising 59 accessions. Unigenes containing the 62 genic-SSRs were searched against Non-redundant (Nr), Gene Ontology database (GO), eukaryotic orthologous groups (KOGs) and Kyoto Encyclopedia of Genes and Genomes (KEGG) database. The search resulted in 53 matching Nr sequences, of which 39 had GO terms, 18 were assigned to KOGs, and 15 were annotated with KEGG. Genetic diversity and population structure were analyzed based on 55 polymorphic genic-SSR data among 59 accessions. The genetic distance averaged 0.3911, ranging from 0.016 to 0.618. The polymorphic index content (PIC) of 55 polymorphic markers averaged 0.407, ranging from 0.033 to 0.863. A model-based clustering analysis revealed that five genetic groups existed in the collection. Accessions from the same species were typically grouped together; however, C. goeringii accessions did not always form a separate cluster, suggesting that C. goeringii accessions were polyphyletic.
The genic-SSR identified in this study constitute a set of markers that can be applied across multiple Cymbidium species and used for the evaluation of genetic relationships as well as qualitative and quantitative trait mapping studies. Genic-SSR's coupled with the functional annotations provided by the unigenes will aid in mapping candidate genes of specific function.
兰属是兰科中一个包含68个物种的属,具有极高的观赏价值。标记辅助选择已被证明是加速许多植物物种育种的有效策略。通过分子标记分析兰花的遗传背景对于辅助亲本选择和育种策略设计具有重要价值,然而,像兰花这类植物的基因组资源有限。为了获得有效的标记,我们对建兰转录组进行了深度测序,以鉴定源自基因区域的简单序列重复(基因SSR)。
共鉴定出7936个基因SSR标记。总共选择了80个基因SSR,并根据其侧翼序列设计了引物。在80个基因SSR引物组中,62个在建兰中成功扩增,55个在包括59份种质的9种兰花物种间交叉检测时表现出多态性。对包含62个基因SSR的单基因簇在非冗余(Nr)、基因本体数据库(GO)、真核直系同源组(KOG)和京都基因与基因组百科全书(KEGG)数据库中进行搜索。搜索结果得到53个匹配的Nr序列,其中39个具有GO术语,18个被分配到KOG,15个用KEGG注释。基于59份种质间55个多态性基因SSR数据进行遗传多样性和群体结构分析。遗传距离平均为0.3911,范围从0.016到0.618。55个多态性标记的多态性信息含量(PIC)平均为0.407,范围从0.033到0.863。基于模型的聚类分析表明,该收集物中存在五个遗传组。同一物种的种质通常聚在一起;然而,春兰种质并不总是形成一个单独的聚类,这表明春兰种质是多系的。
本研究中鉴定的基因SSR构成了一组可应用于多种兰花物种的标记,可用于评估遗传关系以及定性和定量性状定位研究。基因SSR与单基因簇提供的功能注释相结合,将有助于定位特定功能的候选基因。