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Transcriptome sequencing of lentil based on second-generation technology permits large-scale unigene assembly and SSR marker discovery
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 significa...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3113791/ https://www.ncbi.nlm.nih.gov/pubmed/21609489 http://dx.doi.org/10.1186/1471-2164-12-265 |
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author | Kaur, Sukhjiwan Cogan, Noel OI Pembleton, Luke W Shinozuka, Maiko Savin, Keith W Materne, Michael Forster, John W |
author_facet | Kaur, Sukhjiwan Cogan, Noel OI Pembleton, Luke W Shinozuka, Maiko Savin, Keith W Materne, Michael Forster, John W |
author_sort | Kaur, Sukhjiwan |
collection | PubMed |
description | 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 × 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. |
format | Online Article Text |
id | pubmed-3113791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31137912011-06-14 Transcriptome sequencing of lentil based on second-generation technology permits large-scale unigene assembly and SSR marker discovery Kaur, Sukhjiwan Cogan, Noel OI Pembleton, Luke W Shinozuka, Maiko Savin, Keith W Materne, Michael Forster, John W BMC Genomics Research Article 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 × 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. BioMed Central 2011-05-25 /pmc/articles/PMC3113791/ /pubmed/21609489 http://dx.doi.org/10.1186/1471-2164-12-265 Text en Copyright ©2011 Kaur et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kaur, Sukhjiwan Cogan, Noel OI Pembleton, Luke W Shinozuka, Maiko Savin, Keith W Materne, Michael Forster, John W Transcriptome sequencing of lentil based on second-generation technology permits large-scale unigene assembly and SSR marker discovery |
title | Transcriptome sequencing of lentil based on second-generation technology permits large-scale unigene assembly and SSR marker discovery |
title_full | Transcriptome sequencing of lentil based on second-generation technology permits large-scale unigene assembly and SSR marker discovery |
title_fullStr | Transcriptome sequencing of lentil based on second-generation technology permits large-scale unigene assembly and SSR marker discovery |
title_full_unstemmed | Transcriptome sequencing of lentil based on second-generation technology permits large-scale unigene assembly and SSR marker discovery |
title_short | Transcriptome sequencing of lentil based on second-generation technology permits large-scale unigene assembly and SSR marker discovery |
title_sort | transcriptome sequencing of lentil based on second-generation technology permits large-scale unigene assembly and ssr marker discovery |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3113791/ https://www.ncbi.nlm.nih.gov/pubmed/21609489 http://dx.doi.org/10.1186/1471-2164-12-265 |
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