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利用数字差异显示、微阵列和RNA测序数据的综合生物信息学方法筛选和鉴定大豆种子特异性基因。

Screening and identification of soybean seed-specific genes by using integrated bioinformatics of digital differential display, microarray, and RNA-seq data.

作者信息

Yin Guangjun, Xu Hongliang, Liu Jingyi, Gao Cong, Sun Jinyue, Yan Yueming, Hu Yingkao

机构信息

College of Life Sciences, Capital Normal University, Beijing 100048, China.

Biochemistry, Molecular Biology & Biophysics, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

Gene. 2014 Aug 10;546(2):177-86. doi: 10.1016/j.gene.2014.06.021. Epub 2014 Jun 11.

DOI:10.1016/j.gene.2014.06.021
PMID:24929124
Abstract

Soybean is one of the most economically important crops in the world. Soybean seeds have abundant protein and lipid content and very high economic value. In this study, a total of 184 seed-specific genes were obtained using online microarray databases, DDD, and RNA-seq data. The reported seed-specific genes in soybean and the 184 seed-specific genes analyzed in this paper were compared. Of the screened genes, 26 were common to both previous reports and the current screening. Meanwhile, 90 of the 184 genes have homologous counterparts in Arabidopsis, among which 24 have seed-specific expression, as indicated by microarray data for Arabidopsis. Furthermore, promoter analysis showed that almost all seed-specific genes contain at least one seed specific-related element. Seed-specific element Skn-1 motif exists in most, if not all, of the seed-specific genes screened. Five genes were randomly selected from 184 soybean seed specific gene pool and their expressions were quantified using quantitative real time polymerase chain reaction (qRT-PCR) to further confirm the specificity of the screened genes. The results indicated that all five genes showed seed-specific expression. Moreover, the identification of genes with seed-specific expression screened in this study provides information valuable to the in-depth study of soybean.

摘要

大豆是世界上经济价值最重要的作物之一。大豆种子含有丰富的蛋白质和脂质,具有很高的经济价值。在本研究中,利用在线微阵列数据库、DDD和RNA测序数据共获得了184个种子特异性基因。对已报道的大豆种子特异性基因与本文分析的184个种子特异性基因进行了比较。在筛选出的基因中,有26个是先前报道和当前筛选共有的。同时,184个基因中的90个在拟南芥中有同源对应物,其中24个具有种子特异性表达,这由拟南芥的微阵列数据表明。此外,启动子分析表明,几乎所有种子特异性基因都至少包含一个种子特异性相关元件。种子特异性元件Skn-1基序存在于大多数(如果不是全部)筛选出的种子特异性基因中。从184个大豆种子特异性基因库中随机选择5个基因,并用实时定量聚合酶链反应(qRT-PCR)对其表达进行定量,以进一步确认筛选出的基因的特异性。结果表明,所有5个基因均表现出种子特异性表达。此外,本研究中筛选出的具有种子特异性表达的基因的鉴定为大豆的深入研究提供了有价值的信息。

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