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基于刺槐(Robinia pseudoacacia L.)转录组序列开发和评估一组新型EST-SSR标记

Development and Evaluation of a Novel Set of EST-SSR Markers Based on Transcriptome Sequences of Black Locust (Robinia pseudoacacia L.).

作者信息

Guo Qi, Wang Jin-Xing, Su Li-Zhuo, Lv Wei, Sun Yu-Han, Li Yun

机构信息

Beijing Advanced Innovation Center for Tree Breeding by Molecular Design, National Engineering Laboratory for Tree Breeding, College of Biological Sciences and Technology, Beijing Forestry University, Beijing 100083, China.

State-owned Linghai Hongqi Forest, Jinzhou 121228, China.

出版信息

Genes (Basel). 2017 Jul 7;8(7):177. doi: 10.3390/genes8070177.

Abstract

Black locust ( L. of the family Fabaceae) is an ecologically and economically important deciduous tree. However, few genomic resources are available for this forest species, and few effective expressed sequence tag-derived simple sequence repeat (EST-SSR) markers have been developed to date. In this study, paired-end sequencing was used to sequence transcriptomes of R. pseudoacacia by the Illumina HiSeq TM2000 platform, and EST-SSR loci were identified by de novo assembly. Furthermore, a total of 1697 primer pairs were successfully designed, from which 286 primers met the selection screening criteria; 94 pairs were randomly selected and tested for validation using polymerase chain reaction amplification. Forty-five primers were verified as polymorphic, with clear bands. The polymorphism information content values were 0.033-0.765, the number of alleles per locus ranged from 2 to 10, and the observed and expected heterozygosities were 0.000-0.931 and 0.035-0.810, respectively, indicating a high level of informativeness. Subsequently, 45 polymorphic EST-SSR loci were tested for amplification efficiency, using the verified primers, in an additional nine species of Leguminosae, 23 loci were amplified in more than three species, of which two loci were amplified successfully in all species. These EST-SSR markers provide a valuable tool for investigating the genetic diversity and population structure of . , constructing a DNA fingerprint database, performing quantitative trait locus mapping, and preserving genetic information.

摘要

刺槐(豆科刺槐属)是一种具有重要生态和经济价值的落叶乔木。然而,针对这种森林树种的基因组资源却很少,并且迄今为止开发的有效表达序列标签衍生简单序列重复(EST-SSR)标记也很少。在本研究中,通过Illumina HiSeq TM2000平台使用双末端测序对刺槐转录组进行测序,并通过从头组装鉴定EST-SSR位点。此外,成功设计了总共1697对引物,其中286对引物符合筛选标准;随机选择94对引物并使用聚合酶链反应扩增进行验证测试。45对引物被验证为具有多态性,条带清晰。多态性信息含量值为0.033 - 0.765,每个位点的等位基因数范围为2至10,观察到的和预期的杂合度分别为0.000 - 0.931和0.035 - 0.810,表明具有高度信息性。随后,使用经过验证的引物对45个多态性EST-SSR位点在另外9种豆科植物中进行扩增效率测试,23个位点在三种以上物种中扩增成功,其中两个位点在所有物种中均成功扩增。这些EST-SSR标记为研究刺槐的遗传多样性和群体结构、构建DNA指纹数据库、进行数量性状位点定位以及保存遗传信息提供了有价值的工具。

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