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Additive and non-additive genetic variance in juvenile Sitka spruce (Picea sitchensis Bong. Carr)
Many quantitative genetic models assume that all genetic variation is additive because of a lack of data with sufficient structure and quality to determine the relative contribution of additive and non-additive variation. Here the fractions of additive (f(a)) and non-additive (f(d)) genetic variatio...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632294/ https://www.ncbi.nlm.nih.gov/pubmed/37970220 http://dx.doi.org/10.1007/s11295-023-01627-5 |
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author | Ilska, J.J. Tolhurst, D.J. Tumas, H. Maclean, J. P. Cottrell, J. Lee, S.J. Mackay, J. Woolliams, J.A. |
author_facet | Ilska, J.J. Tolhurst, D.J. Tumas, H. Maclean, J. P. Cottrell, J. Lee, S.J. Mackay, J. Woolliams, J.A. |
author_sort | Ilska, J.J. |
collection | PubMed |
description | Many quantitative genetic models assume that all genetic variation is additive because of a lack of data with sufficient structure and quality to determine the relative contribution of additive and non-additive variation. Here the fractions of additive (f(a)) and non-additive (f(d)) genetic variation were estimated in Sitka spruce for height, bud burst and pilodyn penetration depth. Approximately 1500 offspring were produced in each of three sib families and clonally replicated across three geographically diverse sites. Genotypes from 1525 offspring from all three families were obtained by RADseq, followed by imputation using 1630 loci segregating in all families and mapped using the newly developed linkage map of Sitka spruce. The analyses employed a new approach for estimating f(a) and f(d), which combined all available genotypic and phenotypic data with spatial modelling for each trait and site. The consensus estimate for f(a) increased with age for height from 0.58 at 2 years to 0.75 at 11 years, with only small overlap in 95% support intervals (I(95)). The estimated f(a) for bud burst was 0.83 (I(95)=[0.78, 0.90]) and 0.84 (I(95)=[0.77, 0.92]) for pilodyn depth. Overall, there was no evidence of family heterogeneity for height or bud burst, or site heterogeneity for pilodyn depth, and no evidence of inbreeding depression associated with genomic homozygosity, expected if dominance variance was the major component of non-additive variance. The results offer no support for the development of sublines for crossing within the species. The models give new opportunities to assess more accurately the scale of non-additive variation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11295-023-01627-5. |
format | Online Article Text |
id | pubmed-10632294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-106322942023-11-14 Additive and non-additive genetic variance in juvenile Sitka spruce (Picea sitchensis Bong. Carr) Ilska, J.J. Tolhurst, D.J. Tumas, H. Maclean, J. P. Cottrell, J. Lee, S.J. Mackay, J. Woolliams, J.A. Tree Genet Genomes Original Article Many quantitative genetic models assume that all genetic variation is additive because of a lack of data with sufficient structure and quality to determine the relative contribution of additive and non-additive variation. Here the fractions of additive (f(a)) and non-additive (f(d)) genetic variation were estimated in Sitka spruce for height, bud burst and pilodyn penetration depth. Approximately 1500 offspring were produced in each of three sib families and clonally replicated across three geographically diverse sites. Genotypes from 1525 offspring from all three families were obtained by RADseq, followed by imputation using 1630 loci segregating in all families and mapped using the newly developed linkage map of Sitka spruce. The analyses employed a new approach for estimating f(a) and f(d), which combined all available genotypic and phenotypic data with spatial modelling for each trait and site. The consensus estimate for f(a) increased with age for height from 0.58 at 2 years to 0.75 at 11 years, with only small overlap in 95% support intervals (I(95)). The estimated f(a) for bud burst was 0.83 (I(95)=[0.78, 0.90]) and 0.84 (I(95)=[0.77, 0.92]) for pilodyn depth. Overall, there was no evidence of family heterogeneity for height or bud burst, or site heterogeneity for pilodyn depth, and no evidence of inbreeding depression associated with genomic homozygosity, expected if dominance variance was the major component of non-additive variance. The results offer no support for the development of sublines for crossing within the species. The models give new opportunities to assess more accurately the scale of non-additive variation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11295-023-01627-5. Springer Berlin Heidelberg 2023-11-08 2023 /pmc/articles/PMC10632294/ /pubmed/37970220 http://dx.doi.org/10.1007/s11295-023-01627-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Ilska, J.J. Tolhurst, D.J. Tumas, H. Maclean, J. P. Cottrell, J. Lee, S.J. Mackay, J. Woolliams, J.A. Additive and non-additive genetic variance in juvenile Sitka spruce (Picea sitchensis Bong. Carr) |
title | Additive and non-additive genetic variance in juvenile Sitka spruce (Picea sitchensis Bong. Carr) |
title_full | Additive and non-additive genetic variance in juvenile Sitka spruce (Picea sitchensis Bong. Carr) |
title_fullStr | Additive and non-additive genetic variance in juvenile Sitka spruce (Picea sitchensis Bong. Carr) |
title_full_unstemmed | Additive and non-additive genetic variance in juvenile Sitka spruce (Picea sitchensis Bong. Carr) |
title_short | Additive and non-additive genetic variance in juvenile Sitka spruce (Picea sitchensis Bong. Carr) |
title_sort | additive and non-additive genetic variance in juvenile sitka spruce (picea sitchensis bong. carr) |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632294/ https://www.ncbi.nlm.nih.gov/pubmed/37970220 http://dx.doi.org/10.1007/s11295-023-01627-5 |
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