Cargando…
An Axiom SNP genotyping array for Douglas-fir
BACKGROUND: In forest trees, genetic markers have been used to understand the genetic architecture of natural populations, identify quantitative trait loci, infer gene function, and enhance tree breeding. Recently, new, efficient technologies for genotyping thousands to millions of single nucleotide...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942338/ https://www.ncbi.nlm.nih.gov/pubmed/31900111 http://dx.doi.org/10.1186/s12864-019-6383-9 |
_version_ | 1783484684017074176 |
---|---|
author | Howe, Glenn T. Jayawickrama, Keith Kolpak, Scott E. Kling, Jennifer Trappe, Matt Hipkins, Valerie Ye, Terrance Guida, Stephanie Cronn, Richard Cushman, Samuel A. McEvoy, Susan |
author_facet | Howe, Glenn T. Jayawickrama, Keith Kolpak, Scott E. Kling, Jennifer Trappe, Matt Hipkins, Valerie Ye, Terrance Guida, Stephanie Cronn, Richard Cushman, Samuel A. McEvoy, Susan |
author_sort | Howe, Glenn T. |
collection | PubMed |
description | BACKGROUND: In forest trees, genetic markers have been used to understand the genetic architecture of natural populations, identify quantitative trait loci, infer gene function, and enhance tree breeding. Recently, new, efficient technologies for genotyping thousands to millions of single nucleotide polymorphisms (SNPs) have finally made large-scale use of genetic markers widely available. These methods will be exceedingly valuable for improving tree breeding and understanding the ecological genetics of Douglas-fir, one of the most economically and ecologically important trees in the world. RESULTS: We designed SNP assays for 55,766 potential SNPs that were discovered from previous transcriptome sequencing projects. We tested the array on ~ 2300 related and unrelated coastal Douglas-fir trees (Pseudotsuga menziesii var. menziesii) from Oregon and Washington, and 13 trees of interior Douglas-fir (P. menziesii var. glauca). As many as ~ 28 K SNPs were reliably genotyped and polymorphic, depending on the selected SNP call rate. To increase the number of SNPs and improve genome coverage, we developed protocols to ‘rescue’ SNPs that did not pass the default Affymetrix quality control criteria (e.g., 97% SNP call rate). Lowering the SNP call rate threshold from 97 to 60% increased the number of successful SNPs from 20,669 to 28,094. We used a subset of 395 unrelated trees to calculate SNP population genetic statistics for coastal Douglas-fir. Over a range of call rate thresholds (97 to 60%), the median call rate for SNPs in Hardy-Weinberg equilibrium ranged from 99.2 to 99.7%, and the median minor allele frequency ranged from 0.198 to 0.233. The successful SNPs also worked well on interior Douglas-fir. CONCLUSIONS: Based on the original transcriptome assemblies and comparisons to version 1.0 of the Douglas-fir reference genome, we conclude that these SNPs can be used to genotype about 10 K to 15 K loci. The Axiom genotyping array will serve as an excellent foundation for studying the population genomics of Douglas-fir and for implementing genomic selection. We are currently using the array to construct a linkage map and test genomic selection in a three-generation breeding program for coastal Douglas-fir. |
format | Online Article Text |
id | pubmed-6942338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69423382020-01-07 An Axiom SNP genotyping array for Douglas-fir Howe, Glenn T. Jayawickrama, Keith Kolpak, Scott E. Kling, Jennifer Trappe, Matt Hipkins, Valerie Ye, Terrance Guida, Stephanie Cronn, Richard Cushman, Samuel A. McEvoy, Susan BMC Genomics Research Article BACKGROUND: In forest trees, genetic markers have been used to understand the genetic architecture of natural populations, identify quantitative trait loci, infer gene function, and enhance tree breeding. Recently, new, efficient technologies for genotyping thousands to millions of single nucleotide polymorphisms (SNPs) have finally made large-scale use of genetic markers widely available. These methods will be exceedingly valuable for improving tree breeding and understanding the ecological genetics of Douglas-fir, one of the most economically and ecologically important trees in the world. RESULTS: We designed SNP assays for 55,766 potential SNPs that were discovered from previous transcriptome sequencing projects. We tested the array on ~ 2300 related and unrelated coastal Douglas-fir trees (Pseudotsuga menziesii var. menziesii) from Oregon and Washington, and 13 trees of interior Douglas-fir (P. menziesii var. glauca). As many as ~ 28 K SNPs were reliably genotyped and polymorphic, depending on the selected SNP call rate. To increase the number of SNPs and improve genome coverage, we developed protocols to ‘rescue’ SNPs that did not pass the default Affymetrix quality control criteria (e.g., 97% SNP call rate). Lowering the SNP call rate threshold from 97 to 60% increased the number of successful SNPs from 20,669 to 28,094. We used a subset of 395 unrelated trees to calculate SNP population genetic statistics for coastal Douglas-fir. Over a range of call rate thresholds (97 to 60%), the median call rate for SNPs in Hardy-Weinberg equilibrium ranged from 99.2 to 99.7%, and the median minor allele frequency ranged from 0.198 to 0.233. The successful SNPs also worked well on interior Douglas-fir. CONCLUSIONS: Based on the original transcriptome assemblies and comparisons to version 1.0 of the Douglas-fir reference genome, we conclude that these SNPs can be used to genotype about 10 K to 15 K loci. The Axiom genotyping array will serve as an excellent foundation for studying the population genomics of Douglas-fir and for implementing genomic selection. We are currently using the array to construct a linkage map and test genomic selection in a three-generation breeding program for coastal Douglas-fir. BioMed Central 2020-01-03 /pmc/articles/PMC6942338/ /pubmed/31900111 http://dx.doi.org/10.1186/s12864-019-6383-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Howe, Glenn T. Jayawickrama, Keith Kolpak, Scott E. Kling, Jennifer Trappe, Matt Hipkins, Valerie Ye, Terrance Guida, Stephanie Cronn, Richard Cushman, Samuel A. McEvoy, Susan An Axiom SNP genotyping array for Douglas-fir |
title | An Axiom SNP genotyping array for Douglas-fir |
title_full | An Axiom SNP genotyping array for Douglas-fir |
title_fullStr | An Axiom SNP genotyping array for Douglas-fir |
title_full_unstemmed | An Axiom SNP genotyping array for Douglas-fir |
title_short | An Axiom SNP genotyping array for Douglas-fir |
title_sort | axiom snp genotyping array for douglas-fir |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942338/ https://www.ncbi.nlm.nih.gov/pubmed/31900111 http://dx.doi.org/10.1186/s12864-019-6383-9 |
work_keys_str_mv | AT howeglennt anaxiomsnpgenotypingarrayfordouglasfir AT jayawickramakeith anaxiomsnpgenotypingarrayfordouglasfir AT kolpakscotte anaxiomsnpgenotypingarrayfordouglasfir AT klingjennifer anaxiomsnpgenotypingarrayfordouglasfir AT trappematt anaxiomsnpgenotypingarrayfordouglasfir AT hipkinsvalerie anaxiomsnpgenotypingarrayfordouglasfir AT yeterrance anaxiomsnpgenotypingarrayfordouglasfir AT guidastephanie anaxiomsnpgenotypingarrayfordouglasfir AT cronnrichard anaxiomsnpgenotypingarrayfordouglasfir AT cushmansamuela anaxiomsnpgenotypingarrayfordouglasfir AT mcevoysusan anaxiomsnpgenotypingarrayfordouglasfir AT howeglennt axiomsnpgenotypingarrayfordouglasfir AT jayawickramakeith axiomsnpgenotypingarrayfordouglasfir AT kolpakscotte axiomsnpgenotypingarrayfordouglasfir AT klingjennifer axiomsnpgenotypingarrayfordouglasfir AT trappematt axiomsnpgenotypingarrayfordouglasfir AT hipkinsvalerie axiomsnpgenotypingarrayfordouglasfir AT yeterrance axiomsnpgenotypingarrayfordouglasfir AT guidastephanie axiomsnpgenotypingarrayfordouglasfir AT cronnrichard axiomsnpgenotypingarrayfordouglasfir AT cushmansamuela axiomsnpgenotypingarrayfordouglasfir AT mcevoysusan axiomsnpgenotypingarrayfordouglasfir |