Cargando…
The characterization of a new set of EST-derived simple sequence repeat (SSR) markers as a resource for the genetic analysis of Phaseolus vulgaris
BACKGROUND: Over recent years, a growing effort has been made to develop microsatellite markers for the genomic analysis of the common bean (Phaseolus vulgaris) to broaden the knowledge of the molecular genetic basis of this species. The availability of large sets of expressed sequence tags (ESTs) i...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102039/ https://www.ncbi.nlm.nih.gov/pubmed/21554695 http://dx.doi.org/10.1186/1471-2156-12-41 |
_version_ | 1782204335601483776 |
---|---|
author | Garcia, Robertha AV Rangel, Priscila N Brondani, Claudio Martins, Wellington S Melo, Leonardo C Carneiro, Monalisa S Borba, Tereza CO Brondani, Rosana PV |
author_facet | Garcia, Robertha AV Rangel, Priscila N Brondani, Claudio Martins, Wellington S Melo, Leonardo C Carneiro, Monalisa S Borba, Tereza CO Brondani, Rosana PV |
author_sort | Garcia, Robertha AV |
collection | PubMed |
description | BACKGROUND: Over recent years, a growing effort has been made to develop microsatellite markers for the genomic analysis of the common bean (Phaseolus vulgaris) to broaden the knowledge of the molecular genetic basis of this species. The availability of large sets of expressed sequence tags (ESTs) in public databases has given rise to an expedient approach for the identification of SSRs (Simple Sequence Repeats), specifically EST-derived SSRs. In the present work, a battery of new microsatellite markers was obtained from a search of the Phaseolus vulgaris EST database. The diversity, degree of transferability and polymorphism of these markers were tested. RESULTS: From 9,583 valid ESTs, 4,764 had microsatellite motifs, from which 377 were used to design primers, and 302 (80.11%) showed good amplification quality. To analyze transferability, a group of 167 SSRs were tested, and the results showed that they were 82% transferable across at least one species. The highest amplification rates were observed between the species from the Phaseolus (63.7%), Vigna (25.9%), Glycine (19.8%), Medicago (10.2%), Dipterix (6%) and Arachis (1.8%) genera. The average PIC (Polymorphism Information Content) varied from 0.53 for genomic SSRs to 0.47 for EST-SSRs, and the average number of alleles per locus was 4 and 3, respectively. Among the 315 newly tested SSRs in the BJ (BAT93 X Jalo EEP558) population, 24% (76) were polymorphic. The integration of these segregant loci into a framework map composed of 123 previously obtained SSR markers yielded a total of 199 segregant loci, of which 182 (91.5%) were mapped to 14 linkage groups, resulting in a map length of 1,157 cM. CONCLUSIONS: A total of 302 newly developed EST-SSR markers, showing good amplification quality, are available for the genetic analysis of Phaseolus vulgaris. These markers showed satisfactory rates of transferability, especially between species that have great economic and genomic values. Their diversity was comparable to genomic SSRs, and they were incorporated in the common bean reference genetic map, which constitutes an important contribution to and advance in Phaseolus vulgaris genomic research. |
format | Text |
id | pubmed-3102039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31020392011-05-26 The characterization of a new set of EST-derived simple sequence repeat (SSR) markers as a resource for the genetic analysis of Phaseolus vulgaris Garcia, Robertha AV Rangel, Priscila N Brondani, Claudio Martins, Wellington S Melo, Leonardo C Carneiro, Monalisa S Borba, Tereza CO Brondani, Rosana PV BMC Genet Research Article BACKGROUND: Over recent years, a growing effort has been made to develop microsatellite markers for the genomic analysis of the common bean (Phaseolus vulgaris) to broaden the knowledge of the molecular genetic basis of this species. The availability of large sets of expressed sequence tags (ESTs) in public databases has given rise to an expedient approach for the identification of SSRs (Simple Sequence Repeats), specifically EST-derived SSRs. In the present work, a battery of new microsatellite markers was obtained from a search of the Phaseolus vulgaris EST database. The diversity, degree of transferability and polymorphism of these markers were tested. RESULTS: From 9,583 valid ESTs, 4,764 had microsatellite motifs, from which 377 were used to design primers, and 302 (80.11%) showed good amplification quality. To analyze transferability, a group of 167 SSRs were tested, and the results showed that they were 82% transferable across at least one species. The highest amplification rates were observed between the species from the Phaseolus (63.7%), Vigna (25.9%), Glycine (19.8%), Medicago (10.2%), Dipterix (6%) and Arachis (1.8%) genera. The average PIC (Polymorphism Information Content) varied from 0.53 for genomic SSRs to 0.47 for EST-SSRs, and the average number of alleles per locus was 4 and 3, respectively. Among the 315 newly tested SSRs in the BJ (BAT93 X Jalo EEP558) population, 24% (76) were polymorphic. The integration of these segregant loci into a framework map composed of 123 previously obtained SSR markers yielded a total of 199 segregant loci, of which 182 (91.5%) were mapped to 14 linkage groups, resulting in a map length of 1,157 cM. CONCLUSIONS: A total of 302 newly developed EST-SSR markers, showing good amplification quality, are available for the genetic analysis of Phaseolus vulgaris. These markers showed satisfactory rates of transferability, especially between species that have great economic and genomic values. Their diversity was comparable to genomic SSRs, and they were incorporated in the common bean reference genetic map, which constitutes an important contribution to and advance in Phaseolus vulgaris genomic research. BioMed Central 2011-05-09 /pmc/articles/PMC3102039/ /pubmed/21554695 http://dx.doi.org/10.1186/1471-2156-12-41 Text en Copyright ©2011 Garcia 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 Garcia, Robertha AV Rangel, Priscila N Brondani, Claudio Martins, Wellington S Melo, Leonardo C Carneiro, Monalisa S Borba, Tereza CO Brondani, Rosana PV The characterization of a new set of EST-derived simple sequence repeat (SSR) markers as a resource for the genetic analysis of Phaseolus vulgaris |
title | The characterization of a new set of EST-derived simple sequence repeat (SSR) markers as a resource for the genetic analysis of Phaseolus vulgaris |
title_full | The characterization of a new set of EST-derived simple sequence repeat (SSR) markers as a resource for the genetic analysis of Phaseolus vulgaris |
title_fullStr | The characterization of a new set of EST-derived simple sequence repeat (SSR) markers as a resource for the genetic analysis of Phaseolus vulgaris |
title_full_unstemmed | The characterization of a new set of EST-derived simple sequence repeat (SSR) markers as a resource for the genetic analysis of Phaseolus vulgaris |
title_short | The characterization of a new set of EST-derived simple sequence repeat (SSR) markers as a resource for the genetic analysis of Phaseolus vulgaris |
title_sort | characterization of a new set of est-derived simple sequence repeat (ssr) markers as a resource for the genetic analysis of phaseolus vulgaris |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102039/ https://www.ncbi.nlm.nih.gov/pubmed/21554695 http://dx.doi.org/10.1186/1471-2156-12-41 |
work_keys_str_mv | AT garciaroberthaav thecharacterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT rangelpriscilan thecharacterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT brondaniclaudio thecharacterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT martinswellingtons thecharacterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT meloleonardoc thecharacterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT carneiromonalisas thecharacterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT borbaterezaco thecharacterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT brondanirosanapv thecharacterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT garciaroberthaav characterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT rangelpriscilan characterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT brondaniclaudio characterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT martinswellingtons characterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT meloleonardoc characterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT carneiromonalisas characterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT borbaterezaco characterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris AT brondanirosanapv characterizationofanewsetofestderivedsimplesequencerepeatssrmarkersasaresourceforthegeneticanalysisofphaseolusvulgaris |