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A SNP resource for Douglas-fir: de novo transcriptome assembly and SNP detection and validation

BACKGROUND: Douglas-fir (Pseudotsuga menziesii), one of the most economically and ecologically important tree species in the world, also has one of the largest tree breeding programs. Although the coastal and interior varieties of Douglas-fir (vars. menziesii and glauca) are native to North America,...

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Autores principales: Howe, Glenn T, Yu, Jianbin, Knaus, Brian, Cronn, Richard, Kolpak, Scott, Dolan, Peter, Lorenz, W Walter, Dean, Jeffrey FD
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673906/
https://www.ncbi.nlm.nih.gov/pubmed/23445355
http://dx.doi.org/10.1186/1471-2164-14-137
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author Howe, Glenn T
Yu, Jianbin
Knaus, Brian
Cronn, Richard
Kolpak, Scott
Dolan, Peter
Lorenz, W Walter
Dean, Jeffrey FD
author_facet Howe, Glenn T
Yu, Jianbin
Knaus, Brian
Cronn, Richard
Kolpak, Scott
Dolan, Peter
Lorenz, W Walter
Dean, Jeffrey FD
author_sort Howe, Glenn T
collection PubMed
description BACKGROUND: Douglas-fir (Pseudotsuga menziesii), one of the most economically and ecologically important tree species in the world, also has one of the largest tree breeding programs. Although the coastal and interior varieties of Douglas-fir (vars. menziesii and glauca) are native to North America, the coastal variety is also widely planted for timber production in Europe, New Zealand, Australia, and Chile. Our main goal was to develop a SNP resource large enough to facilitate genomic selection in Douglas-fir breeding programs. To accomplish this, we developed a 454-based reference transcriptome for coastal Douglas-fir, annotated and evaluated the quality of the reference, identified putative SNPs, and then validated a sample of those SNPs using the Illumina Infinium genotyping platform. RESULTS: We assembled a reference transcriptome consisting of 25,002 isogroups (unique gene models) and 102,623 singletons from 2.76 million 454 and Sanger cDNA sequences from coastal Douglas-fir. We identified 278,979 unique SNPs by mapping the 454 and Sanger sequences to the reference, and by mapping four datasets of Illumina cDNA sequences from multiple seed sources, genotypes, and tissues. The Illumina datasets represented coastal Douglas-fir (64.00 and 13.41 million reads), interior Douglas-fir (80.45 million reads), and a Yakima population similar to interior Douglas-fir (8.99 million reads). We assayed 8067 SNPs on 260 trees using an Illumina Infinium SNP genotyping array. Of these SNPs, 5847 (72.5%) were called successfully and were polymorphic. CONCLUSIONS: Based on our validation efficiency, our SNP database may contain as many as ~200,000 true SNPs, and as many as ~69,000 SNPs that could be genotyped at ~20,000 gene loci using an Infinium II array—more SNPs than are needed to use genomic selection in tree breeding programs. Ultimately, these genomic resources will enhance Douglas-fir breeding and allow us to better understand landscape-scale patterns of genetic variation and potential responses to climate change.
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spelling pubmed-36739062013-06-06 A SNP resource for Douglas-fir: de novo transcriptome assembly and SNP detection and validation Howe, Glenn T Yu, Jianbin Knaus, Brian Cronn, Richard Kolpak, Scott Dolan, Peter Lorenz, W Walter Dean, Jeffrey FD BMC Genomics Research Article BACKGROUND: Douglas-fir (Pseudotsuga menziesii), one of the most economically and ecologically important tree species in the world, also has one of the largest tree breeding programs. Although the coastal and interior varieties of Douglas-fir (vars. menziesii and glauca) are native to North America, the coastal variety is also widely planted for timber production in Europe, New Zealand, Australia, and Chile. Our main goal was to develop a SNP resource large enough to facilitate genomic selection in Douglas-fir breeding programs. To accomplish this, we developed a 454-based reference transcriptome for coastal Douglas-fir, annotated and evaluated the quality of the reference, identified putative SNPs, and then validated a sample of those SNPs using the Illumina Infinium genotyping platform. RESULTS: We assembled a reference transcriptome consisting of 25,002 isogroups (unique gene models) and 102,623 singletons from 2.76 million 454 and Sanger cDNA sequences from coastal Douglas-fir. We identified 278,979 unique SNPs by mapping the 454 and Sanger sequences to the reference, and by mapping four datasets of Illumina cDNA sequences from multiple seed sources, genotypes, and tissues. The Illumina datasets represented coastal Douglas-fir (64.00 and 13.41 million reads), interior Douglas-fir (80.45 million reads), and a Yakima population similar to interior Douglas-fir (8.99 million reads). We assayed 8067 SNPs on 260 trees using an Illumina Infinium SNP genotyping array. Of these SNPs, 5847 (72.5%) were called successfully and were polymorphic. CONCLUSIONS: Based on our validation efficiency, our SNP database may contain as many as ~200,000 true SNPs, and as many as ~69,000 SNPs that could be genotyped at ~20,000 gene loci using an Infinium II array—more SNPs than are needed to use genomic selection in tree breeding programs. Ultimately, these genomic resources will enhance Douglas-fir breeding and allow us to better understand landscape-scale patterns of genetic variation and potential responses to climate change. BioMed Central 2013-02-28 /pmc/articles/PMC3673906/ /pubmed/23445355 http://dx.doi.org/10.1186/1471-2164-14-137 Text en Copyright © 2013 Howe 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
Howe, Glenn T
Yu, Jianbin
Knaus, Brian
Cronn, Richard
Kolpak, Scott
Dolan, Peter
Lorenz, W Walter
Dean, Jeffrey FD
A SNP resource for Douglas-fir: de novo transcriptome assembly and SNP detection and validation
title A SNP resource for Douglas-fir: de novo transcriptome assembly and SNP detection and validation
title_full A SNP resource for Douglas-fir: de novo transcriptome assembly and SNP detection and validation
title_fullStr A SNP resource for Douglas-fir: de novo transcriptome assembly and SNP detection and validation
title_full_unstemmed A SNP resource for Douglas-fir: de novo transcriptome assembly and SNP detection and validation
title_short A SNP resource for Douglas-fir: de novo transcriptome assembly and SNP detection and validation
title_sort snp resource for douglas-fir: de novo transcriptome assembly and snp detection and validation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673906/
https://www.ncbi.nlm.nih.gov/pubmed/23445355
http://dx.doi.org/10.1186/1471-2164-14-137
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