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Genomic profiling of plastid DNA variation in the Mediterranean olive tree

BACKGROUND: Characterisation of plastid genome (or cpDNA) polymorphisms is commonly used for phylogeographic, population genetic and forensic analyses in plants, but detecting cpDNA variation is sometimes challenging, limiting the applications of such an approach. In the present study, we screened c...

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Autores principales: Besnard, Guillaume, Hernández, Pilar, Khadari, Bouchaib, Dorado, Gabriel, Savolainen, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3115843/
https://www.ncbi.nlm.nih.gov/pubmed/21569271
http://dx.doi.org/10.1186/1471-2229-11-80
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author Besnard, Guillaume
Hernández, Pilar
Khadari, Bouchaib
Dorado, Gabriel
Savolainen, Vincent
author_facet Besnard, Guillaume
Hernández, Pilar
Khadari, Bouchaib
Dorado, Gabriel
Savolainen, Vincent
author_sort Besnard, Guillaume
collection PubMed
description BACKGROUND: Characterisation of plastid genome (or cpDNA) polymorphisms is commonly used for phylogeographic, population genetic and forensic analyses in plants, but detecting cpDNA variation is sometimes challenging, limiting the applications of such an approach. In the present study, we screened cpDNA polymorphism in the olive tree (Olea europaea L.) by sequencing the complete plastid genome of trees with a distinct cpDNA lineage. Our objective was to develop new markers for a rapid genomic profiling (by Multiplex PCRs) of cpDNA haplotypes in the Mediterranean olive tree. RESULTS: Eight complete cpDNA genomes of Olea were sequenced de novo. The nucleotide divergence between olive cpDNA lineages was low and not exceeding 0.07%. Based on these sequences, markers were developed for studying two single nucleotide substitutions and length polymorphism of 62 regions (with variable microsatellite motifs or other indels). They were then used to genotype the cpDNA variation in cultivated and wild Mediterranean olive trees (315 individuals). Forty polymorphic loci were detected on this sample, allowing the distinction of 22 haplotypes belonging to the three Mediterranean cpDNA lineages known as E1, E2 and E3. The discriminating power of cpDNA variation was particularly low for the cultivated olive tree with one predominating haplotype, but more diversity was detected in wild populations. CONCLUSIONS: We propose a method for a rapid characterisation of the Mediterranean olive germplasm. The low variation in the cultivated olive tree indicated that the utility of cpDNA variation for forensic analyses is limited to rare haplotypes. In contrast, the high cpDNA variation in wild populations demonstrated that our markers may be useful for phylogeographic and populations genetic studies in O. europaea.
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spelling pubmed-31158432011-06-16 Genomic profiling of plastid DNA variation in the Mediterranean olive tree Besnard, Guillaume Hernández, Pilar Khadari, Bouchaib Dorado, Gabriel Savolainen, Vincent BMC Plant Biol Methodology Article BACKGROUND: Characterisation of plastid genome (or cpDNA) polymorphisms is commonly used for phylogeographic, population genetic and forensic analyses in plants, but detecting cpDNA variation is sometimes challenging, limiting the applications of such an approach. In the present study, we screened cpDNA polymorphism in the olive tree (Olea europaea L.) by sequencing the complete plastid genome of trees with a distinct cpDNA lineage. Our objective was to develop new markers for a rapid genomic profiling (by Multiplex PCRs) of cpDNA haplotypes in the Mediterranean olive tree. RESULTS: Eight complete cpDNA genomes of Olea were sequenced de novo. The nucleotide divergence between olive cpDNA lineages was low and not exceeding 0.07%. Based on these sequences, markers were developed for studying two single nucleotide substitutions and length polymorphism of 62 regions (with variable microsatellite motifs or other indels). They were then used to genotype the cpDNA variation in cultivated and wild Mediterranean olive trees (315 individuals). Forty polymorphic loci were detected on this sample, allowing the distinction of 22 haplotypes belonging to the three Mediterranean cpDNA lineages known as E1, E2 and E3. The discriminating power of cpDNA variation was particularly low for the cultivated olive tree with one predominating haplotype, but more diversity was detected in wild populations. CONCLUSIONS: We propose a method for a rapid characterisation of the Mediterranean olive germplasm. The low variation in the cultivated olive tree indicated that the utility of cpDNA variation for forensic analyses is limited to rare haplotypes. In contrast, the high cpDNA variation in wild populations demonstrated that our markers may be useful for phylogeographic and populations genetic studies in O. europaea. BioMed Central 2011-05-10 /pmc/articles/PMC3115843/ /pubmed/21569271 http://dx.doi.org/10.1186/1471-2229-11-80 Text en Copyright ©2011 Besnard 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 Methodology Article
Besnard, Guillaume
Hernández, Pilar
Khadari, Bouchaib
Dorado, Gabriel
Savolainen, Vincent
Genomic profiling of plastid DNA variation in the Mediterranean olive tree
title Genomic profiling of plastid DNA variation in the Mediterranean olive tree
title_full Genomic profiling of plastid DNA variation in the Mediterranean olive tree
title_fullStr Genomic profiling of plastid DNA variation in the Mediterranean olive tree
title_full_unstemmed Genomic profiling of plastid DNA variation in the Mediterranean olive tree
title_short Genomic profiling of plastid DNA variation in the Mediterranean olive tree
title_sort genomic profiling of plastid dna variation in the mediterranean olive tree
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3115843/
https://www.ncbi.nlm.nih.gov/pubmed/21569271
http://dx.doi.org/10.1186/1471-2229-11-80
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