FST index and quantitative trait loci (QTL) mapping tools to detect a major genetic determinant involved in geminivirus accumulation. [P.13]

The genetic determinism of viral traits is classically determined by comparing the genomes associated to distinct phenotypes (forward genetics) or by detecting phenotypic variations induced by genetic changes at particular loci (reverse genetics). These approaches might be limited for viral traits determined by several loci or genes which may additionally interact epistatically. Even in the presence of a major determinant, the iterative nature of these procedures can be very time-consuming if no candidate genomic region is identified. In eukaryotes, complex determinisms can be analyzed on recombinant progenies using population-based association studies based on quantitative trait loci (QTL) and fixation indexes (FST) measured at each locus. As QTL approaches need recombinant progenies, they have so far not been used for clonal organisms like viruses. However, these approaches might be extended to highly recombinogenic viruses or more generally to viruses for which genome-wide artificial recombination can generate infectious genomes. Here, we took advantage of the first virus library of genome-wide shuffled recombinant genomes (Proteus, Nimes) between Tomato yellow leaf curl virus (TYLCV-Mld) and Tomato leaf curl Mayotte virus (ToLCKMV). The bimodal distribution of virus accumulation in tomato plants for 47 recombinant genomes (Vuillaume et al. 2011) generated between Tomato yellow leaf curl virus (TYLCV-Mld) and Tomato leaf curl Mayotte virus (ToLCKMV) pointed towards a major genetic determinant of viral accumulation (Vuillaume et al. 2011) that we searched in a genome wide association study. Four QTL methods and the locus-by-locus FST approach were used to identify the regions of the begomovirus genome determining the within-host accumulation. Our results revealed that the viral accumulation in recombinant genomes was determined by loci at the 5' end of the Replication associated protein gene (rep) and the Intergenic Region upstream of the rep. Using classical virology approaches, this region was previously reported to be involved in viral accumulation. The consistency between our results and those previously generated with classical approaches suggests that the QTL and FST approaches could be valuable tools to identify loci involved in viral traits, which holds promises for the characterization of traits with a more complex genetic determinism when appropriate material and data are available.

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Main Authors: Doumayrou, Juliette, Thébaud, Gaël, Peterschmitt, Michel, Vuillaume, Florence, Urbino, Cica
Format: conference_item biblioteca
Language:eng
Published: s.n.
Subjects:H20 - Maladies des plantes, U30 - Méthodes de recherche, F30 - Génétique et amélioration des plantes,
Online Access:http://agritrop.cirad.fr/575831/
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spelling dig-cirad-fr-5758312022-04-15T09:42:41Z http://agritrop.cirad.fr/575831/ http://agritrop.cirad.fr/575831/ FST index and quantitative trait loci (QTL) mapping tools to detect a major genetic determinant involved in geminivirus accumulation. [P.13]. Doumayrou Juliette, Thébaud Gaël, Peterschmitt Michel, Vuillaume Florence, Urbino Cica. 2015. In : 15èmes Rencontres de Virologie Végétale, Aussois, France, 18-22 janvier 2015. CIRAD ; IRD. s.l. : s.n., Résumé, 71. Rencontres de virologie végétale. 15, Aussois, France, 18 Janvier 2015/22 Janvier 2015. Researchers FST index and quantitative trait loci (QTL) mapping tools to detect a major genetic determinant involved in geminivirus accumulation. [P.13] Doumayrou, Juliette Thébaud, Gaël Peterschmitt, Michel Vuillaume, Florence Urbino, Cica eng 2015 s.n. 15èmes Rencontres de Virologie Végétale, Aussois, France, 18-22 janvier 2015 H20 - Maladies des plantes U30 - Méthodes de recherche F30 - Génétique et amélioration des plantes The genetic determinism of viral traits is classically determined by comparing the genomes associated to distinct phenotypes (forward genetics) or by detecting phenotypic variations induced by genetic changes at particular loci (reverse genetics). These approaches might be limited for viral traits determined by several loci or genes which may additionally interact epistatically. Even in the presence of a major determinant, the iterative nature of these procedures can be very time-consuming if no candidate genomic region is identified. In eukaryotes, complex determinisms can be analyzed on recombinant progenies using population-based association studies based on quantitative trait loci (QTL) and fixation indexes (FST) measured at each locus. As QTL approaches need recombinant progenies, they have so far not been used for clonal organisms like viruses. However, these approaches might be extended to highly recombinogenic viruses or more generally to viruses for which genome-wide artificial recombination can generate infectious genomes. Here, we took advantage of the first virus library of genome-wide shuffled recombinant genomes (Proteus, Nimes) between Tomato yellow leaf curl virus (TYLCV-Mld) and Tomato leaf curl Mayotte virus (ToLCKMV). The bimodal distribution of virus accumulation in tomato plants for 47 recombinant genomes (Vuillaume et al. 2011) generated between Tomato yellow leaf curl virus (TYLCV-Mld) and Tomato leaf curl Mayotte virus (ToLCKMV) pointed towards a major genetic determinant of viral accumulation (Vuillaume et al. 2011) that we searched in a genome wide association study. Four QTL methods and the locus-by-locus FST approach were used to identify the regions of the begomovirus genome determining the within-host accumulation. Our results revealed that the viral accumulation in recombinant genomes was determined by loci at the 5' end of the Replication associated protein gene (rep) and the Intergenic Region upstream of the rep. Using classical virology approaches, this region was previously reported to be involved in viral accumulation. The consistency between our results and those previously generated with classical approaches suggests that the QTL and FST approaches could be valuable tools to identify loci involved in viral traits, which holds promises for the characterization of traits with a more complex genetic determinism when appropriate material and data are available. conference_item info:eu-repo/semantics/conferenceObject Conference info:eu-repo/semantics/closedAccess
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 H20 - Maladies des plantes
U30 - Méthodes de recherche
F30 - Génétique et amélioration des plantes
H20 - Maladies des plantes
U30 - Méthodes de recherche
F30 - Génétique et amélioration des plantes
spellingShingle H20 - Maladies des plantes
U30 - Méthodes de recherche
F30 - Génétique et amélioration des plantes
H20 - Maladies des plantes
U30 - Méthodes de recherche
F30 - Génétique et amélioration des plantes
Doumayrou, Juliette
Thébaud, Gaël
Peterschmitt, Michel
Vuillaume, Florence
Urbino, Cica
FST index and quantitative trait loci (QTL) mapping tools to detect a major genetic determinant involved in geminivirus accumulation. [P.13]
description The genetic determinism of viral traits is classically determined by comparing the genomes associated to distinct phenotypes (forward genetics) or by detecting phenotypic variations induced by genetic changes at particular loci (reverse genetics). These approaches might be limited for viral traits determined by several loci or genes which may additionally interact epistatically. Even in the presence of a major determinant, the iterative nature of these procedures can be very time-consuming if no candidate genomic region is identified. In eukaryotes, complex determinisms can be analyzed on recombinant progenies using population-based association studies based on quantitative trait loci (QTL) and fixation indexes (FST) measured at each locus. As QTL approaches need recombinant progenies, they have so far not been used for clonal organisms like viruses. However, these approaches might be extended to highly recombinogenic viruses or more generally to viruses for which genome-wide artificial recombination can generate infectious genomes. Here, we took advantage of the first virus library of genome-wide shuffled recombinant genomes (Proteus, Nimes) between Tomato yellow leaf curl virus (TYLCV-Mld) and Tomato leaf curl Mayotte virus (ToLCKMV). The bimodal distribution of virus accumulation in tomato plants for 47 recombinant genomes (Vuillaume et al. 2011) generated between Tomato yellow leaf curl virus (TYLCV-Mld) and Tomato leaf curl Mayotte virus (ToLCKMV) pointed towards a major genetic determinant of viral accumulation (Vuillaume et al. 2011) that we searched in a genome wide association study. Four QTL methods and the locus-by-locus FST approach were used to identify the regions of the begomovirus genome determining the within-host accumulation. Our results revealed that the viral accumulation in recombinant genomes was determined by loci at the 5' end of the Replication associated protein gene (rep) and the Intergenic Region upstream of the rep. Using classical virology approaches, this region was previously reported to be involved in viral accumulation. The consistency between our results and those previously generated with classical approaches suggests that the QTL and FST approaches could be valuable tools to identify loci involved in viral traits, which holds promises for the characterization of traits with a more complex genetic determinism when appropriate material and data are available.
format conference_item
topic_facet H20 - Maladies des plantes
U30 - Méthodes de recherche
F30 - Génétique et amélioration des plantes
author Doumayrou, Juliette
Thébaud, Gaël
Peterschmitt, Michel
Vuillaume, Florence
Urbino, Cica
author_facet Doumayrou, Juliette
Thébaud, Gaël
Peterschmitt, Michel
Vuillaume, Florence
Urbino, Cica
author_sort Doumayrou, Juliette
title FST index and quantitative trait loci (QTL) mapping tools to detect a major genetic determinant involved in geminivirus accumulation. [P.13]
title_short FST index and quantitative trait loci (QTL) mapping tools to detect a major genetic determinant involved in geminivirus accumulation. [P.13]
title_full FST index and quantitative trait loci (QTL) mapping tools to detect a major genetic determinant involved in geminivirus accumulation. [P.13]
title_fullStr FST index and quantitative trait loci (QTL) mapping tools to detect a major genetic determinant involved in geminivirus accumulation. [P.13]
title_full_unstemmed FST index and quantitative trait loci (QTL) mapping tools to detect a major genetic determinant involved in geminivirus accumulation. [P.13]
title_sort fst index and quantitative trait loci (qtl) mapping tools to detect a major genetic determinant involved in geminivirus accumulation. [p.13]
publisher s.n.
url http://agritrop.cirad.fr/575831/
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