Analysis of Gene Expression Profiles in Leaf Tissues of Cultivated Peanuts and Development of EST-SSR Markers and Gene Discovery.

International journal of plant genomics Pub Date : 2009-01-01 Epub Date: 2009-06-24 DOI:10.1155/2009/715605
Baozhu Guo, Xiaoping Chen, Yanbin Hong, Xuanqiang Liang, Phat Dang, Tim Brenneman, Corley Holbrook, Albert Culbreath
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Abstract

Peanut is vulnerable to a range of foliar diseases such as spotted wilt caused by Tomato spotted wilt virus (TSWV), early (Cercospora arachidicola) and late (Cercosporidium personatum) leaf spots, southern stem rot (Sclerotium rolfsii), and sclerotinia blight (Sclerotinia minor). In this study, we report the generation of 17,376 peanut expressed sequence tags (ESTs) from leaf tissues of a peanut cultivar (Tifrunner, resistant to TSWV and leaf spots) and a breeding line (GT-C20, susceptible to TSWV and leaf spots). After trimming vector and discarding low quality sequences, a total of 14,432 high-quality ESTs were selected for further analysis and deposition to GenBank. Sequence clustering resulted in 6,888 unique ESTs composed of 1,703 tentative consensus (TCs) sequences and 5185 singletons. A large number of ESTs (5717) representing genes of unknown functions were also identified. Among the unique sequences, there were 856 EST-SSRs identified. A total of 290 new EST-based SSR markers were developed and examined for amplification and polymorphism in cultivated peanut and wild species. Resequencing information of selected amplified alleles revealed that allelic diversity could be attributed mainly to differences in repeat type and length in the SSR regions. In addition, a few additional INDEL mutations and substitutions were observed in the regions flanking the microsatellite regions. In addition, some defense-related transcripts were also identified, such as putative oxalate oxidase (EU024476) and NBS-LRR domains. EST data in this study have provided a new source of information for gene discovery and development of SSR markers in cultivated peanut. A total of 16931 ESTs have been deposited to the NCBI GenBank database with accession numbers ES751523 to ES768453.

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分析栽培花生叶组织的基因表达谱并开发 EST-SSR 标记和基因发现。
花生易受一系列叶面病害的侵袭,如番茄斑萎病毒(TSWV)引起的斑萎病、早期叶斑病(Cercospora arachidicola)和晚期叶斑病(Cercosporidium personatum)、南方茎腐病(Sclerotium rolfsii)和枯萎病(Sclerotinia minor)。在这项研究中,我们报告了从一个花生栽培品种(Tifrunner,抗 TSWV 和叶斑病)和一个育种品系(GT-C20,易感 TSWV 和叶斑病)的叶组织中生成的 17,376 个花生表达序列标签(ESTs)。在修剪载体和剔除低质量序列后,共挑选出 14,432 个高质量 EST 进行进一步分析,并将其存入 GenBank。通过序列聚类,得到了 6,888 个独特的ESTs,其中包括 1,703 个暂定共识(TC)序列和 5185 个单体序列。此外,还发现了大量代表未知功能基因的ESTs(5717个)。在这些独特序列中,共鉴定出 856 个 EST-SSR。共开发了 290 个基于 EST 的新 SSR 标记,并对其在栽培花生和野生物种中的扩增和多态性进行了检验。对所选扩增等位基因的重测序信息显示,等位基因的多样性主要归因于 SSR 区域中重复类型和长度的差异。此外,在微卫星区域的侧翼还观察到一些额外的 INDEL 突变和置换。此外,还发现了一些与防御相关的转录本,如推测的草酸氧化酶(EU024476)和 NBS-LRR 结构域。本研究的EST数据为发现栽培花生的基因和开发SSR标记提供了新的信息来源。共有 16931 个 EST 保存在 NCBI GenBank 数据库中,登录号为 ES751523 至 ES768453。
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