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

被引:142
|
作者
Kaur, Sukhjiwan [1 ]
Cogan, Noel O. I. [1 ]
Pembleton, Luke W. [1 ]
Shinozuka, Maiko [1 ]
Savin, Keith W. [1 ]
Materne, Michael [2 ]
Forster, John W. [1 ,3 ]
机构
[1] La Trobe Univ Res & Dev Pk, Dept Primary Ind, Biosci Res Div, Victorian AgriBiosci Ctr, Bundoora, Vic 3083, Australia
[2] Grains Innovat Pk, Dept Primary Ind, Biosci Res Div, Horsham, Vic 3401, Australia
[3] La Trobe Univ, Bundoora, Vic 3086, Australia
来源
BMC GENOMICS | 2011年 / 12卷
关键词
MEDICAGO-TRUNCATULA; EST-SSRS; GENOME; MICROSATELLITES; PLANT; TAGS; ANNOTATION; FREQUENCY; RESOURCE; REPEATS;
D O I
10.1186/1471-2164-12-265
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 x 10(6) 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.
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页数:11
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