文献类型： 外文期刊
作者： Hou, Wanwei 1 ; Zhang, Xiaojuan 3 ; Liu, Yuling 2 ; Liu, Yujiao 2 ; Feng, Bai Li 1 ;
作者机构： 1.Northwest A&F Univ, Coll Agron, Yangling, Shaanxi, Peoples R China
2.Qinghai Univ, Qinghai Acad Agr & Forestry Sci, Xining, Qinghai, Peoples R China
3.Qinghai Univ, Coll Ecoenvironm Engn, Xining, Qinghai, Peoples R China
关键词： Keywords Vicia faba L; RNA-Seq; Gene function analysis; Simple sequence repeats (SSR) markers
期刊名称：PEERJ （ 影响因子：2.7； 五年影响因子：3.1 ）
ISSN： 2167-8359
年卷期： 2023 年 11 卷
页码：
收录情况： SCI
摘要： Background. Faba bean (Vicia faba L) is one of the most important legumes in the world. However, there is relatively little genomic information available for this species owing to its large genome. The lack of data impedes the discovery of molecular markers and subsequent genetic research in faba bean. The objective of this study was to analyze the faba bean transcriptome, and to develop simple sequence repeat (SSR) markers to determine the genetic diversity of 226 faba bean varieties derived from different regions in China. Methods. Faba bean varieties with different phenotype were used in transcriptome analysis. The functions of the unigenes were analyzed using various database. SSR markers were developed and the polymorphic markers were selected to conduct genetic diversity analysis.Results. A total of 92.43 Gb of sequencing data was obtained in this study, and 133,487 unigene sequences with a total length of 178,152,541 bp were assembled. A total of 5,200 SSR markers were developed on the basis of RNA-Seq analysis. Then, 200 SSR markers were used to evaluate polymorphisms. In total, 103 (51.5%) SSR markers showed significant and repeatable bands between different faba bean varieties. Clustering analysis revealed that 226 faba bean materials were divided into five groups. Genetic diversity analysis revealed that the relationship between different faba beans in China was related, especially in the same region. These results provided a valuable data resource for annotating genes to different categories and developing SSR markers.
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