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Model SNP development for complex genomes based on hexaploid oat using high-throughput 454 sequencing technology

BACKGROUND: Genetic markers are pivotal to modern genomics research; however, discovery and genotyping of molecular markers in oat has been hindered by the size and complexity of the genome, and by a scarcity of sequence data. The purpose of this study was to generate oat expressed sequence tag (EST...

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Autores principales: Oliver, Rebekah E, Lazo, Gerard R, Lutz, Joseph D, Rubenfield, Marc J, Tinker, Nicholas A, Anderson, Joseph M, Wisniewski Morehead, Nicole H, Adhikary, Dinesh, Jellen, Eric N, Maughan, P Jeffrey, Brown Guedira, Gina L, Chao, Shiaoman, Beattie, Aaron D, Carson, Martin L, Rines, Howard W, Obert, Donald E, Bonman, J Michael, Jackson, Eric W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041746/
https://www.ncbi.nlm.nih.gov/pubmed/21272354
http://dx.doi.org/10.1186/1471-2164-12-77
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author Oliver, Rebekah E
Lazo, Gerard R
Lutz, Joseph D
Rubenfield, Marc J
Tinker, Nicholas A
Anderson, Joseph M
Wisniewski Morehead, Nicole H
Adhikary, Dinesh
Jellen, Eric N
Maughan, P Jeffrey
Brown Guedira, Gina L
Chao, Shiaoman
Beattie, Aaron D
Carson, Martin L
Rines, Howard W
Obert, Donald E
Bonman, J Michael
Jackson, Eric W
author_facet Oliver, Rebekah E
Lazo, Gerard R
Lutz, Joseph D
Rubenfield, Marc J
Tinker, Nicholas A
Anderson, Joseph M
Wisniewski Morehead, Nicole H
Adhikary, Dinesh
Jellen, Eric N
Maughan, P Jeffrey
Brown Guedira, Gina L
Chao, Shiaoman
Beattie, Aaron D
Carson, Martin L
Rines, Howard W
Obert, Donald E
Bonman, J Michael
Jackson, Eric W
author_sort Oliver, Rebekah E
collection PubMed
description BACKGROUND: Genetic markers are pivotal to modern genomics research; however, discovery and genotyping of molecular markers in oat has been hindered by the size and complexity of the genome, and by a scarcity of sequence data. The purpose of this study was to generate oat expressed sequence tag (EST) information, develop a bioinformatics pipeline for SNP discovery, and establish a method for rapid, cost-effective, and straightforward genotyping of SNP markers in complex polyploid genomes such as oat. RESULTS: Based on cDNA libraries of four cultivated oat genotypes, approximately 127,000 contigs were assembled from approximately one million Roche 454 sequence reads. Contigs were filtered through a novel bioinformatics pipeline to eliminate ambiguous polymorphism caused by subgenome homology, and 96 in silico SNPs were selected from 9,448 candidate loci for validation using high-resolution melting (HRM) analysis. Of these, 52 (54%) were polymorphic between parents of the Ogle1040 × TAM O-301 (OT) mapping population, with 48 segregating as single Mendelian loci, and 44 being placed on the existing OT linkage map. Ogle and TAM amplicons from 12 primers were sequenced for SNP validation, revealing complex polymorphism in seven amplicons but general sequence conservation within SNP loci. Whole-amplicon interrogation with HRM revealed insertions, deletions, and heterozygotes in secondary oat germplasm pools, generating multiple alleles at some primer targets. To validate marker utility, 36 SNP assays were used to evaluate the genetic diversity of 34 diverse oat genotypes. Dendrogram clusters corresponded generally to known genome composition and genetic ancestry. CONCLUSIONS: The high-throughput SNP discovery pipeline presented here is a rapid and effective method for identification of polymorphic SNP alleles in the oat genome. The current-generation HRM system is a simple and highly-informative platform for SNP genotyping. These techniques provide a model for SNP discovery and genotyping in other species with complex and poorly-characterized genomes.
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spelling pubmed-30417462011-02-19 Model SNP development for complex genomes based on hexaploid oat using high-throughput 454 sequencing technology Oliver, Rebekah E Lazo, Gerard R Lutz, Joseph D Rubenfield, Marc J Tinker, Nicholas A Anderson, Joseph M Wisniewski Morehead, Nicole H Adhikary, Dinesh Jellen, Eric N Maughan, P Jeffrey Brown Guedira, Gina L Chao, Shiaoman Beattie, Aaron D Carson, Martin L Rines, Howard W Obert, Donald E Bonman, J Michael Jackson, Eric W BMC Genomics Research Article BACKGROUND: Genetic markers are pivotal to modern genomics research; however, discovery and genotyping of molecular markers in oat has been hindered by the size and complexity of the genome, and by a scarcity of sequence data. The purpose of this study was to generate oat expressed sequence tag (EST) information, develop a bioinformatics pipeline for SNP discovery, and establish a method for rapid, cost-effective, and straightforward genotyping of SNP markers in complex polyploid genomes such as oat. RESULTS: Based on cDNA libraries of four cultivated oat genotypes, approximately 127,000 contigs were assembled from approximately one million Roche 454 sequence reads. Contigs were filtered through a novel bioinformatics pipeline to eliminate ambiguous polymorphism caused by subgenome homology, and 96 in silico SNPs were selected from 9,448 candidate loci for validation using high-resolution melting (HRM) analysis. Of these, 52 (54%) were polymorphic between parents of the Ogle1040 × TAM O-301 (OT) mapping population, with 48 segregating as single Mendelian loci, and 44 being placed on the existing OT linkage map. Ogle and TAM amplicons from 12 primers were sequenced for SNP validation, revealing complex polymorphism in seven amplicons but general sequence conservation within SNP loci. Whole-amplicon interrogation with HRM revealed insertions, deletions, and heterozygotes in secondary oat germplasm pools, generating multiple alleles at some primer targets. To validate marker utility, 36 SNP assays were used to evaluate the genetic diversity of 34 diverse oat genotypes. Dendrogram clusters corresponded generally to known genome composition and genetic ancestry. CONCLUSIONS: The high-throughput SNP discovery pipeline presented here is a rapid and effective method for identification of polymorphic SNP alleles in the oat genome. The current-generation HRM system is a simple and highly-informative platform for SNP genotyping. These techniques provide a model for SNP discovery and genotyping in other species with complex and poorly-characterized genomes. BioMed Central 2011-01-27 /pmc/articles/PMC3041746/ /pubmed/21272354 http://dx.doi.org/10.1186/1471-2164-12-77 Text en Copyright ©2011 Oliver 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
Oliver, Rebekah E
Lazo, Gerard R
Lutz, Joseph D
Rubenfield, Marc J
Tinker, Nicholas A
Anderson, Joseph M
Wisniewski Morehead, Nicole H
Adhikary, Dinesh
Jellen, Eric N
Maughan, P Jeffrey
Brown Guedira, Gina L
Chao, Shiaoman
Beattie, Aaron D
Carson, Martin L
Rines, Howard W
Obert, Donald E
Bonman, J Michael
Jackson, Eric W
Model SNP development for complex genomes based on hexaploid oat using high-throughput 454 sequencing technology
title Model SNP development for complex genomes based on hexaploid oat using high-throughput 454 sequencing technology
title_full Model SNP development for complex genomes based on hexaploid oat using high-throughput 454 sequencing technology
title_fullStr Model SNP development for complex genomes based on hexaploid oat using high-throughput 454 sequencing technology
title_full_unstemmed Model SNP development for complex genomes based on hexaploid oat using high-throughput 454 sequencing technology
title_short Model SNP development for complex genomes based on hexaploid oat using high-throughput 454 sequencing technology
title_sort model snp development for complex genomes based on hexaploid oat using high-throughput 454 sequencing technology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041746/
https://www.ncbi.nlm.nih.gov/pubmed/21272354
http://dx.doi.org/10.1186/1471-2164-12-77
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