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基于第二代技术的兵豆转录组测序可实现大规模的基因组装和 SSR 标记发现。

Transcriptome sequencing of lentil based on second-generation technology permits large-scale unigene assembly and SSR marker discovery.

机构信息

Department of Primary Industries, Biosciences Research Division, Victorian AgriBiosciences Centre, La Trobe University Research and Development Park, Bundoora, Australia.

出版信息

BMC Genomics. 2011 May 25;12:265. doi: 10.1186/1471-2164-12-265.

Abstract

BACKGROUND

Lentil (Lens culinaris Medik.) is a cool-season grain legume which provides a rich source of protein for human consumption. In terms of genomic resources, lentil is relatively underdeveloped, in comparison to other Fabaceae species, with limited available data. There is hence a significant need to enhance such resources in order to identify novel genes and alleles for molecular breeding to increase crop productivity and quality.

RESULTS

Tissue-specific cDNA samples from six distinct lentil genotypes were sequenced using Roche 454 GS-FLX Titanium technology, generating c. 1.38 × 106 expressed sequence tags (ESTs). De novo assembly generated a total of 15,354 contigs and 68,715 singletons. The complete unigene set was sequence-analysed against genome drafts of the model legume species Medicago truncatula and Arabidopsis thaliana to identify 12,639, and 7,476 unique matches, respectively. When compared to the genome of Glycine max, a total of 20,419 unique hits were observed corresponding to c. 31% of the known gene space. A total of 25,592 lentil unigenes were subsequently annoated from GenBank. Simple sequence repeat (SSR)-containing ESTs were identified from consensus sequences and a total of 2,393 primer pairs were designed. A subset of 192 EST-SSR markers was screened for validation across a panel 12 cultivated lentil genotypes and one wild relative species. A total of 166 primer pairs obtained successful amplification, of which 47.5% detected genetic polymorphism.

CONCLUSIONS

A substantial collection of ESTs has been developed from sequence analysis of lentil genotypes using second-generation technology, permitting unigene definition across a broad range of functional categories. As well as providing resources for functional genomics studies, the unigene set has permitted significant enhancement of the number of publicly-available molecular genetic markers as tools for improvement of this species.

摘要

背景

兵豆(Lens culinaris Medik.)是一种冷季粮食豆科植物,可为人类提供丰富的蛋白质来源。就基因组资源而言,兵豆与其他豆科物种相比相对不发达,可用数据有限。因此,需要显著增强这些资源,以便鉴定用于分子育种的新基因和等位基因,从而提高作物的生产力和质量。

结果

使用 Roche 454 GS-FLX Titanium 技术对来自六个不同兵豆基因型的组织特异性 cDNA 样本进行测序,生成约 1.38×106 个表达序列标签(EST)。从头组装共生成 15354 个 contigs 和 68715 个 singletons。完整的 unigene 集与模式豆科物种蒺藜苜蓿和拟南芥的基因组草案进行序列分析,分别鉴定出 12639 和 7476 个独特匹配。与大豆基因组相比,共观察到 20419 个独特的匹配,对应已知基因空间的约 31%。总共从 GenBank 对 25592 个兵豆 unigene 进行了注释。从共识序列中鉴定出含有简单序列重复(SSR)的 EST,并设计了总共 2393 对引物。在一个 12 个栽培兵豆基因型和一个野生亲缘种的面板中筛选了 192 个 EST-SSR 标记的一个子集进行验证。共获得了 166 对成功扩增的引物,其中 47.5%检测到遗传多态性。

结论

使用第二代技术对兵豆基因型进行序列分析,开发了大量的 EST,可在广泛的功能类别中定义 unigene。除了为功能基因组学研究提供资源外,unigene 集还显著增加了可用于改进该物种的公开分子遗传标记数量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7197/3113791/f45760baa591/1471-2164-12-265-1.jpg

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