Construction of two genetic linkage maps of taro using single nucleotide polymorphism and microsatellite markers

Linkage maps are needed for genetic studies and molecular breeding of taro (Colocasia esculenta). In this study, we used genotyping-by-sequencing (GBS) to identify single nucleotide polymorphism (SNP) loci on two mapping populations: F31 (HLB11 × VU006) composed of 266 progenies and F32 [HLB01 × (VU370×ID316)] composed of 292 progenies. SNP calling generated an initial set of 22,734 SNPs for F31 and 16,744 for F32. A large proportion of individuals and loci were later removed by filtering on the proportion of missing data and segregation distortions. Linkage maps were constructed with filtered SNPs in association with 14 simple sequence repeat (SSR) markers, using the maximum likelihood method. In both populations, loci were successfully grouped into 14 linkage groups (LGs) with an independence logarithm of odds (LOD) threshold of 11.0 and 8.0 for F31 and F32, respectively. LGs ranged in size from 90 to 15 markers for F31 and from 92 to 12 markers for F32. Bridge markers (459 SNPs and 9 SSRs) were identified and revealed homologous groups between families. Although our maps presented unprecedented chromosome coverage, the colinearity between homologous groups was low (except for LG07), and map lengths were globally inflated. Putative effects of missing data, segregation distortion, and genotyping errors on map accuracy are discussed. This research work led to the identification of a reliable set of SNPs potentially useful as a tool for a wide range of genetic studies in taro.

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Main Authors: Soulard, Laurent, Mournet, Pierre, Guitton, Baptiste, Chaïr, Hâna
Format: article biblioteca
Language:eng
Subjects:F30 - Génétique et amélioration des plantes, Colocasia esculenta, carte génétique, séquence nucléotidique, polymorphisme génétique, marqueur génétique, microsatellite, http://aims.fao.org/aos/agrovoc/c_1765, http://aims.fao.org/aos/agrovoc/c_24002, http://aims.fao.org/aos/agrovoc/c_27583, http://aims.fao.org/aos/agrovoc/c_24031, http://aims.fao.org/aos/agrovoc/c_24030, http://aims.fao.org/aos/agrovoc/c_36574,
Online Access:http://agritrop.cirad.fr/583976/
http://agritrop.cirad.fr/583976/1/Soulard_MolBreed2017.pdf
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spelling dig-cirad-fr-5839762024-01-29T00:12:49Z http://agritrop.cirad.fr/583976/ http://agritrop.cirad.fr/583976/ Construction of two genetic linkage maps of taro using single nucleotide polymorphism and microsatellite markers. Soulard Laurent, Mournet Pierre, Guitton Baptiste, Chaïr Hâna. 2017. Molecular Breeding, 37 (3):37, 15 p.https://doi.org/10.1007/s11032-017-0646-4 <https://doi.org/10.1007/s11032-017-0646-4> Construction of two genetic linkage maps of taro using single nucleotide polymorphism and microsatellite markers Soulard, Laurent Mournet, Pierre Guitton, Baptiste Chaïr, Hâna eng 2017 Molecular Breeding F30 - Génétique et amélioration des plantes Colocasia esculenta carte génétique séquence nucléotidique polymorphisme génétique marqueur génétique microsatellite http://aims.fao.org/aos/agrovoc/c_1765 http://aims.fao.org/aos/agrovoc/c_24002 http://aims.fao.org/aos/agrovoc/c_27583 http://aims.fao.org/aos/agrovoc/c_24031 http://aims.fao.org/aos/agrovoc/c_24030 http://aims.fao.org/aos/agrovoc/c_36574 Linkage maps are needed for genetic studies and molecular breeding of taro (Colocasia esculenta). In this study, we used genotyping-by-sequencing (GBS) to identify single nucleotide polymorphism (SNP) loci on two mapping populations: F31 (HLB11 × VU006) composed of 266 progenies and F32 [HLB01 × (VU370×ID316)] composed of 292 progenies. SNP calling generated an initial set of 22,734 SNPs for F31 and 16,744 for F32. A large proportion of individuals and loci were later removed by filtering on the proportion of missing data and segregation distortions. Linkage maps were constructed with filtered SNPs in association with 14 simple sequence repeat (SSR) markers, using the maximum likelihood method. In both populations, loci were successfully grouped into 14 linkage groups (LGs) with an independence logarithm of odds (LOD) threshold of 11.0 and 8.0 for F31 and F32, respectively. LGs ranged in size from 90 to 15 markers for F31 and from 92 to 12 markers for F32. Bridge markers (459 SNPs and 9 SSRs) were identified and revealed homologous groups between families. Although our maps presented unprecedented chromosome coverage, the colinearity between homologous groups was low (except for LG07), and map lengths were globally inflated. Putative effects of missing data, segregation distortion, and genotyping errors on map accuracy are discussed. This research work led to the identification of a reliable set of SNPs potentially useful as a tool for a wide range of genetic studies in taro. article info:eu-repo/semantics/article Journal Article info:eu-repo/semantics/publishedVersion http://agritrop.cirad.fr/583976/1/Soulard_MolBreed2017.pdf text Cirad license info:eu-repo/semantics/restrictedAccess https://agritrop.cirad.fr/mention_legale.html https://doi.org/10.1007/s11032-017-0646-4 10.1007/s11032-017-0646-4 info:eu-repo/semantics/altIdentifier/doi/10.1007/s11032-017-0646-4 info:eu-repo/semantics/altIdentifier/purl/https://doi.org/10.1007/s11032-017-0646-4
institution CIRAD FR
collection DSpace
country Francia
countrycode FR
component Bibliográfico
access En linea
databasecode dig-cirad-fr
tag biblioteca
region Europa del Oeste
libraryname Biblioteca del CIRAD Francia
language eng
topic F30 - Génétique et amélioration des plantes
Colocasia esculenta
carte génétique
séquence nucléotidique
polymorphisme génétique
marqueur génétique
microsatellite
http://aims.fao.org/aos/agrovoc/c_1765
http://aims.fao.org/aos/agrovoc/c_24002
http://aims.fao.org/aos/agrovoc/c_27583
http://aims.fao.org/aos/agrovoc/c_24031
http://aims.fao.org/aos/agrovoc/c_24030
http://aims.fao.org/aos/agrovoc/c_36574
F30 - Génétique et amélioration des plantes
Colocasia esculenta
carte génétique
séquence nucléotidique
polymorphisme génétique
marqueur génétique
microsatellite
http://aims.fao.org/aos/agrovoc/c_1765
http://aims.fao.org/aos/agrovoc/c_24002
http://aims.fao.org/aos/agrovoc/c_27583
http://aims.fao.org/aos/agrovoc/c_24031
http://aims.fao.org/aos/agrovoc/c_24030
http://aims.fao.org/aos/agrovoc/c_36574
spellingShingle F30 - Génétique et amélioration des plantes
Colocasia esculenta
carte génétique
séquence nucléotidique
polymorphisme génétique
marqueur génétique
microsatellite
http://aims.fao.org/aos/agrovoc/c_1765
http://aims.fao.org/aos/agrovoc/c_24002
http://aims.fao.org/aos/agrovoc/c_27583
http://aims.fao.org/aos/agrovoc/c_24031
http://aims.fao.org/aos/agrovoc/c_24030
http://aims.fao.org/aos/agrovoc/c_36574
F30 - Génétique et amélioration des plantes
Colocasia esculenta
carte génétique
séquence nucléotidique
polymorphisme génétique
marqueur génétique
microsatellite
http://aims.fao.org/aos/agrovoc/c_1765
http://aims.fao.org/aos/agrovoc/c_24002
http://aims.fao.org/aos/agrovoc/c_27583
http://aims.fao.org/aos/agrovoc/c_24031
http://aims.fao.org/aos/agrovoc/c_24030
http://aims.fao.org/aos/agrovoc/c_36574
Soulard, Laurent
Mournet, Pierre
Guitton, Baptiste
Chaïr, Hâna
Construction of two genetic linkage maps of taro using single nucleotide polymorphism and microsatellite markers
description Linkage maps are needed for genetic studies and molecular breeding of taro (Colocasia esculenta). In this study, we used genotyping-by-sequencing (GBS) to identify single nucleotide polymorphism (SNP) loci on two mapping populations: F31 (HLB11 × VU006) composed of 266 progenies and F32 [HLB01 × (VU370×ID316)] composed of 292 progenies. SNP calling generated an initial set of 22,734 SNPs for F31 and 16,744 for F32. A large proportion of individuals and loci were later removed by filtering on the proportion of missing data and segregation distortions. Linkage maps were constructed with filtered SNPs in association with 14 simple sequence repeat (SSR) markers, using the maximum likelihood method. In both populations, loci were successfully grouped into 14 linkage groups (LGs) with an independence logarithm of odds (LOD) threshold of 11.0 and 8.0 for F31 and F32, respectively. LGs ranged in size from 90 to 15 markers for F31 and from 92 to 12 markers for F32. Bridge markers (459 SNPs and 9 SSRs) were identified and revealed homologous groups between families. Although our maps presented unprecedented chromosome coverage, the colinearity between homologous groups was low (except for LG07), and map lengths were globally inflated. Putative effects of missing data, segregation distortion, and genotyping errors on map accuracy are discussed. This research work led to the identification of a reliable set of SNPs potentially useful as a tool for a wide range of genetic studies in taro.
format article
topic_facet F30 - Génétique et amélioration des plantes
Colocasia esculenta
carte génétique
séquence nucléotidique
polymorphisme génétique
marqueur génétique
microsatellite
http://aims.fao.org/aos/agrovoc/c_1765
http://aims.fao.org/aos/agrovoc/c_24002
http://aims.fao.org/aos/agrovoc/c_27583
http://aims.fao.org/aos/agrovoc/c_24031
http://aims.fao.org/aos/agrovoc/c_24030
http://aims.fao.org/aos/agrovoc/c_36574
author Soulard, Laurent
Mournet, Pierre
Guitton, Baptiste
Chaïr, Hâna
author_facet Soulard, Laurent
Mournet, Pierre
Guitton, Baptiste
Chaïr, Hâna
author_sort Soulard, Laurent
title Construction of two genetic linkage maps of taro using single nucleotide polymorphism and microsatellite markers
title_short Construction of two genetic linkage maps of taro using single nucleotide polymorphism and microsatellite markers
title_full Construction of two genetic linkage maps of taro using single nucleotide polymorphism and microsatellite markers
title_fullStr Construction of two genetic linkage maps of taro using single nucleotide polymorphism and microsatellite markers
title_full_unstemmed Construction of two genetic linkage maps of taro using single nucleotide polymorphism and microsatellite markers
title_sort construction of two genetic linkage maps of taro using single nucleotide polymorphism and microsatellite markers
url http://agritrop.cirad.fr/583976/
http://agritrop.cirad.fr/583976/1/Soulard_MolBreed2017.pdf
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AT guittonbaptiste constructionoftwogeneticlinkagemapsoftarousingsinglenucleotidepolymorphismandmicrosatellitemarkers
AT chairhana constructionoftwogeneticlinkagemapsoftarousingsinglenucleotidepolymorphismandmicrosatellitemarkers
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