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利用 Illumina 配对末端测序进行从头组装和根转录组学分析,并开发甘薯(Ipomoea batatas)中的 cSSR 标记。

De novo assembly and characterization of root transcriptome using Illumina paired-end sequencing and development of cSSR markers in sweet potato (Ipomoea batatas).

机构信息

Crops Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou, 510640 PR China.

出版信息

BMC Genomics. 2010 Dec 24;11:726. doi: 10.1186/1471-2164-11-726.

Abstract

BACKGROUND

The tuberous root of sweet potato is an important agricultural and biological organ. There are not sufficient transcriptomic and genomic data in public databases for understanding of the molecular mechanism underlying the tuberous root formation and development. Thus, high throughput transcriptome sequencing is needed to generate enormous transcript sequences from sweet potato root for gene discovery and molecular marker development.

RESULTS

In this study, more than 59 million sequencing reads were generated using Illumina paired-end sequencing technology. De novo assembly yielded 56,516 unigenes with an average length of 581 bp. Based on sequence similarity search with known proteins, a total of 35,051 (62.02%) genes were identified. Out of these annotated unigenes, 5,046 and 11,983 unigenes were assigned to gene ontology and clusters of orthologous group, respectively. Searching against the Kyoto Encyclopedia of Genes and Genomes Pathway database (KEGG) indicated that 17,598 (31.14%) unigenes were mapped to 124 KEGG pathways, and 11,056 were assigned to metabolic pathways, which were well represented by carbohydrate metabolism and biosynthesis of secondary metabolite. In addition, 4,114 cDNA SSRs (cSSRs) were identified as potential molecular markers in our unigenes. One hundred pairs of PCR primers were designed and used for validation of the amplification and assessment of the polymorphism in genomic DNA pools. The result revealed that 92 primer pairs were successfully amplified in initial screening tests.

CONCLUSION

This study generated a substantial fraction of sweet potato transcript sequences, which can be used to discover novel genes associated with tuberous root formation and development and will also make it possible to construct high density microarrays for further characterization of gene expression profiles during these processes. Thousands of cSSR markers identified in the present study can enrich molecular markers and will facilitate marker-assisted selection in sweet potato breeding. Overall, these sequences and markers will provide valuable resources for the sweet potato community. Additionally, these results also suggested that transcriptome analysis based on Illumina paired-end sequencing is a powerful tool for gene discovery and molecular marker development for non-model species, especially those with large and complex genome.

摘要

背景

甘薯块根是一种重要的农业和生物器官。由于公共数据库中缺乏足够的转录组和基因组数据来了解块根形成和发育的分子机制,因此需要高通量转录组测序来从甘薯根中生成大量的转录序列,以用于基因发现和分子标记开发。

结果

本研究使用 Illumina 配对末端测序技术生成了超过 5900 万条测序reads。从头组装生成了 56516 个平均长度为 581bp 的 unigenes。基于与已知蛋白质的序列相似性搜索,共鉴定出 35051 个(62.02%)基因。在这些注释的 unigenes中,5046 个和 11983 个 unigenes分别被分配到基因本体和直系同源群聚类。KEGG 数据库(KEGG)分析表明,17598 个(31.14%)unigenes被映射到 124 个 KEGG 途径,11056 个被分配到代谢途径,其中碳水化合物代谢和次生代谢物生物合成得到了很好的代表。此外,在我们的 unigenes中鉴定出 4114 个 cDNA SSRs(cSSR)作为潜在的分子标记。设计了 100 对 PCR 引物用于扩增验证和基因组 DNA 池的多态性评估。结果表明,在初步筛选试验中成功扩增了 92 对引物。

结论

本研究生成了大量的甘薯转录序列,可用于发现与块根形成和发育相关的新基因,并有可能构建高密度微阵列,进一步研究这些过程中的基因表达谱。本研究中鉴定的数千个 cSSR 标记可以丰富分子标记,有助于甘薯育种中的标记辅助选择。总的来说,这些序列和标记将为甘薯社区提供有价值的资源。此外,这些结果还表明,基于 Illumina 配对末端测序的转录组分析是发现非模式物种基因和开发分子标记的有力工具,特别是那些基因组大而复杂的物种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dec8/3016421/e7ce37bcd5a4/1471-2164-11-726-1.jpg

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