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利用 Illumina 测序进行橡胶树(Hevea brasiliensis Muell. Arg.)树皮转录组从头组装和特征分析,并开发 EST-SSR 标记。

De novo assembly and characterization of bark transcriptome using Illumina sequencing and development of EST-SSR markers in rubber tree (Hevea brasiliensis Muell. Arg.).

机构信息

Key Laboratory of Biology and Genetic Resources of Rubber Tree, Ministry of Agriculture, Rubber Research Institute, Chinese Academy of Tropical Agricultural Sciences, Danzhou, Hainan, China.

出版信息

BMC Genomics. 2012 May 18;13:192. doi: 10.1186/1471-2164-13-192.

Abstract

BACKGROUND

In rubber tree, bark is one of important agricultural and biological organs. However, the molecular mechanism involved in the bark formation and development in rubber tree remains largely unknown, which is at least partially due to lack of bark transcriptomic and genomic information. Therefore, it is necessary to carried out high-throughput transcriptome sequencing of rubber tree bark to generate enormous transcript sequences for the functional characterization and molecular marker development.

RESULTS

In this study, more than 30 million sequencing reads were generated using Illumina paired-end sequencing technology. In total, 22,756 unigenes with an average length of 485 bp were obtained with de novo assembly. The similarity search indicated that 16,520 and 12,558 unigenes showed significant similarities to known proteins from NCBI non-redundant and Swissprot protein databases, respectively. Among these annotated unigenes, 6,867 and 5,559 unigenes were separately assigned to Gene Ontology (GO) and Clusters of Orthologous Group (COG). When 22,756 unigenes searched against the Kyoto Encyclopedia of Genes and Genomes Pathway (KEGG) database, 12,097 unigenes were assigned to 5 main categories including 123 KEGG pathways. Among the main KEGG categories, metabolism was the biggest category (9,043, 74.75%), suggesting the active metabolic processes in rubber tree bark. In addition, a total of 39,257 EST-SSRs were identified from 22,756 unigenes, and the characterizations of EST-SSRs were further analyzed in rubber tree. 110 potential marker sites were randomly selected to validate the assembly quality and develop EST-SSR markers. Among 13 Hevea germplasms, PCR success rate and polymorphism rate of 110 markers were separately 96.36% and 55.45% in this study.

CONCLUSION

By assembling and analyzing de novo transcriptome sequencing data, we reported the comprehensive functional characterization of rubber tree bark. This research generated a substantial fraction of rubber tree transcriptome sequences, which were very useful resources for gene annotation and discovery, molecular markers development, genome assembly and annotation, and microarrays development in rubber tree. The EST-SSR markers identified and developed in this study will facilitate marker-assisted selection breeding in rubber tree. Moreover, this study also supported that transcriptome analysis based on Illumina paired-end sequencing is a powerful tool for transcriptome characterization and molecular marker development in non-model species, especially those with large and complex genomes.

摘要

背景

在橡胶树中,树皮是重要的农业和生物器官之一。然而,橡胶树树皮形成和发育的分子机制在很大程度上仍然未知,这至少部分是由于缺乏树皮转录组和基因组信息。因此,有必要对橡胶树树皮进行高通量转录组测序,以产生大量的转录序列,用于功能表征和分子标记的开发。

结果

在这项研究中,使用 Illumina 配对末端测序技术生成了 3000 多万个测序reads。总共获得了 22756 个具有 485bp 平均长度的 unigenes,通过从头组装获得。相似性搜索表明,16520 和 12558 个 unigenes分别与 NCBI 非冗余和 Swissprot 蛋白质数据库中的已知蛋白质具有显著相似性。在这些注释的 unigenes中,6867 和 5559 个 unigenes分别被分配到基因本体论(GO)和直系同源群(COG)。当将 22756 个 unigenes搜索京都基因与基因组百科全书(KEGG)数据库时,12097 个 unigenes被分配到包括 123 个 KEGG 途径在内的 5 个主要类别中。在主要的 KEGG 类别中,代谢是最大的类别(9043,74.75%),表明橡胶树树皮中的代谢活动活跃。此外,从 22756 个 unigenes中共鉴定了 39257 个 EST-SSR,进一步分析了橡胶树中 EST-SSR 的特征。从 22756 个 unigenes中随机选择了 110 个潜在的标记位点来验证组装质量并开发 EST-SSR 标记。在 13 个 Hevea 种质中,本研究中 110 个标记的 PCR 成功率和多态性率分别为 96.36%和 55.45%。

结论

通过组装和分析从头转录组测序数据,我们报告了橡胶树树皮的综合功能特征。本研究产生了大量的橡胶树转录组序列,这些序列对于基因注释和发现、分子标记开发、橡胶树基因组组装和注释以及微阵列开发非常有用。本研究中鉴定和开发的 EST-SSR 标记将有助于橡胶树的标记辅助选择育种。此外,本研究还表明,基于 Illumina 配对末端测序的转录组分析是一种强大的工具,可用于非模式物种的转录组特征描述和分子标记开发,特别是那些具有大而复杂基因组的物种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1537/3431226/4c6d651729ea/1471-2164-13-192-1.jpg

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