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Genetic variation of six desaturase genes in flax and their impact on fatty acid composition

Flax (Linum usitatissimum L.) is one of the richest plant sources of omega-3 fatty acids praised for their health benefits. In this study, the extent of the genetic variability of genes encoding stearoyl-ACP desaturase (SAD), and fatty acid desaturase 2 (FAD2) and 3 (FAD3) was determined by sequenci...

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Autores principales: Thambugala, Dinushika, Duguid, Scott, Loewen, Evelyn, Rowland, Gordon, Booker, Helen, You, Frank M., Cloutier, Sylvie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782649/
https://www.ncbi.nlm.nih.gov/pubmed/23928861
http://dx.doi.org/10.1007/s00122-013-2161-2
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author Thambugala, Dinushika
Duguid, Scott
Loewen, Evelyn
Rowland, Gordon
Booker, Helen
You, Frank M.
Cloutier, Sylvie
author_facet Thambugala, Dinushika
Duguid, Scott
Loewen, Evelyn
Rowland, Gordon
Booker, Helen
You, Frank M.
Cloutier, Sylvie
author_sort Thambugala, Dinushika
collection PubMed
description Flax (Linum usitatissimum L.) is one of the richest plant sources of omega-3 fatty acids praised for their health benefits. In this study, the extent of the genetic variability of genes encoding stearoyl-ACP desaturase (SAD), and fatty acid desaturase 2 (FAD2) and 3 (FAD3) was determined by sequencing the six paralogous genes from 120 flax accessions representing a broad range of germplasm including some EMS mutant lines. A total of 6 alleles for sad1 and sad2, 21 for fad2a, 5 for fad2b, 15 for fad3a and 18 for fad3b were identified. Deduced amino acid sequences of the alleles predicted 4, 2, 3, 4, 6 and 7 isoforms, respectively. Allele frequencies varied greatly across genes. Fad3a, with 110 SNPs and 19 indels, and fad3b, with 50 SNPs and 5 indels, showed the highest levels of genetic variations. While most of the SNPs and all the indels were silent mutations, both genes carried nonsense SNP mutations resulting in premature stop codons, a feature not observed in sad and fad2 genes. Some alleles and isoforms discovered in induced mutant lines were absent in the natural germplasm. Correlation of these genotypic data with fatty acid composition data of 120 flax accessions phenotyped in six field experiments revealed statistically significant effects of some of the SAD and FAD isoforms on fatty acid composition, oil content and iodine value. The novel allelic variants and isoforms identified for the six desaturases will be a resource for the development of oilseed flax with unique and useful fatty acid profiles. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00122-013-2161-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-37826492013-09-25 Genetic variation of six desaturase genes in flax and their impact on fatty acid composition Thambugala, Dinushika Duguid, Scott Loewen, Evelyn Rowland, Gordon Booker, Helen You, Frank M. Cloutier, Sylvie Theor Appl Genet Original Paper Flax (Linum usitatissimum L.) is one of the richest plant sources of omega-3 fatty acids praised for their health benefits. In this study, the extent of the genetic variability of genes encoding stearoyl-ACP desaturase (SAD), and fatty acid desaturase 2 (FAD2) and 3 (FAD3) was determined by sequencing the six paralogous genes from 120 flax accessions representing a broad range of germplasm including some EMS mutant lines. A total of 6 alleles for sad1 and sad2, 21 for fad2a, 5 for fad2b, 15 for fad3a and 18 for fad3b were identified. Deduced amino acid sequences of the alleles predicted 4, 2, 3, 4, 6 and 7 isoforms, respectively. Allele frequencies varied greatly across genes. Fad3a, with 110 SNPs and 19 indels, and fad3b, with 50 SNPs and 5 indels, showed the highest levels of genetic variations. While most of the SNPs and all the indels were silent mutations, both genes carried nonsense SNP mutations resulting in premature stop codons, a feature not observed in sad and fad2 genes. Some alleles and isoforms discovered in induced mutant lines were absent in the natural germplasm. Correlation of these genotypic data with fatty acid composition data of 120 flax accessions phenotyped in six field experiments revealed statistically significant effects of some of the SAD and FAD isoforms on fatty acid composition, oil content and iodine value. The novel allelic variants and isoforms identified for the six desaturases will be a resource for the development of oilseed flax with unique and useful fatty acid profiles. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00122-013-2161-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2013-08-09 2013 /pmc/articles/PMC3782649/ /pubmed/23928861 http://dx.doi.org/10.1007/s00122-013-2161-2 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Paper
Thambugala, Dinushika
Duguid, Scott
Loewen, Evelyn
Rowland, Gordon
Booker, Helen
You, Frank M.
Cloutier, Sylvie
Genetic variation of six desaturase genes in flax and their impact on fatty acid composition
title Genetic variation of six desaturase genes in flax and their impact on fatty acid composition
title_full Genetic variation of six desaturase genes in flax and their impact on fatty acid composition
title_fullStr Genetic variation of six desaturase genes in flax and their impact on fatty acid composition
title_full_unstemmed Genetic variation of six desaturase genes in flax and their impact on fatty acid composition
title_short Genetic variation of six desaturase genes in flax and their impact on fatty acid composition
title_sort genetic variation of six desaturase genes in flax and their impact on fatty acid composition
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782649/
https://www.ncbi.nlm.nih.gov/pubmed/23928861
http://dx.doi.org/10.1007/s00122-013-2161-2
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