QTL mapping in new Arabidopsis thaliana advanced intercross-recombinant inbred lines

dc.contributor.authorBalasubramanian, Sureshkumar
dc.contributor.authorSchwartz, Christopher J.
dc.contributor.authorSingh, Anandita
dc.contributor.authorWarthmann, Norman
dc.contributor.authorKim, Min Chul
dc.contributor.authorMaloof, Julin N.
dc.contributor.authorLoudet, Olivier
dc.contributor.authorTrainer, Gabriel T.
dc.contributor.authorDabi, Tsegaye
dc.contributor.authorBorevitz, Justin O.
dc.contributor.authorChory, Joanne
dc.contributor.authorWeigel, Detlef
dc.date.accessioned2015-11-23T00:16:36Z
dc.date.available2015-11-23T00:16:36Z
dc.date.issued2009-02-02
dc.date.updated2015-12-11T10:32:54Z
dc.description.abstractBACKGROUND Even when phenotypic differences are large between natural or domesticated strains, the underlying genetic basis is often complex, and causal genomic regions need to be identified by quantitative trait locus (QTL) mapping. Unfortunately, QTL positions typically have large confidence intervals, which can, for example, lead to one QTL being masked by another, when two closely linked loci are detected as a single QTL. One strategy to increase the power of precisely localizing small effect QTL, is the use of an intercross approach before inbreeding to produce Advanced Intercross RILs (AI-RILs). METHODOLOGY/PRINCIPAL FINDINGS We present two new AI-RIL populations of Arabidopsis thaliana genotyped with an average intermarker distance of 600 kb. The advanced intercrossing design led to expansion of the genetic map in the two populations, which contain recombination events corresponding to 50 kb/cM in an F(2) population. We used the AI-RILs to map QTL for light response and flowering time, and to identify segregation distortion in one of the AI-RIL populations due to a negative epistatic interaction between two genomic regions. CONCLUSIONS/SIGNIFICANCE The two new AI-RIL populations, EstC and KendC, derived from crosses of Columbia (Col) to Estland (Est-1) and Kendallville (Kend-L) provide an excellent resource for high precision QTL mapping. Moreover, because they have been genotyped with over 100 common markers, they are also excellent material for comparative QTL mapping.
dc.description.sponsorshipThis work was supported by NIH NRSA Grant F23-GM65032-1 (CS), an EMBO Long-Term Fellowship ALTF-473 (SB), NIH grant GM62932 (JC & DW), ERAPG (BMBF) Grant ARABRAS, and a Gottfried Wilhelm Leibniz Award from the DFG (DW), the Howard Hughes Medical Institute, and the Max Planck Society.en_AU
dc.format8 pages
dc.identifier.issn1932-6203en_AU
dc.identifier.urihttp://hdl.handle.net/1885/16594
dc.publisherPublic Library of Science
dc.rights© 2009 Balasubramanian et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
dc.sourcePLoS ONE
dc.subjectarabidopsis
dc.subjectchromosome mapping
dc.subjectchromosomes, plant
dc.subjectepistasis, genetic
dc.subjectflowers
dc.subjectgenes, plant
dc.subjectgenome, plant
dc.subjectgenotype
dc.subjecthypocotyl
dc.subjectplants, genetically modified
dc.subjectquantitative trait loci
dc.subjectcrosses, genetic
dc.titleQTL mapping in new Arabidopsis thaliana advanced intercross-recombinant inbred lines
dc.typeJournal article
dcterms.dateAccepted2008-12-22
local.bibliographicCitation.issue2en_AU
local.bibliographicCitation.lastpage8
local.bibliographicCitation.startpagee4318en_AU
local.contributor.affiliationBalasubramanian, Sureshkumar , Max Planck Institute for Developmental Biology, Germanyen_AU
local.contributor.affiliationSchwartz, Christopher J., Salk Institute for Biological Studies, United States of Americaen_AU
local.contributor.affiliationSingh, Anandita, Max Planck Institute for Developmental Biology, Germanyen_AU
local.contributor.affiliationWarthmann, Norman, College of Medicine, Biology and Environment, CMBE Research School of Biology, Division of Plant Sciences, The Australian National Universityen_AU
local.contributor.affiliationKim, Min Chul, Max Planck Institute for Developmental Biology, Germanyen_AU
local.contributor.affiliationMaloof, Julin N, University of California, United States of Americaen_AU
local.contributor.affiliationLoudet, Olivier, The Salk Institute for Biological Sciences,, United States of Americaen_AU
local.contributor.affiliationTrainer, Gabriel T., The Salk Institute for Biological Sciences, United States of Americaen_AU
local.contributor.affiliationDabi, Tsegaye, The Salk Institute for Biological Sciences,, United States of Americaen_AU
local.contributor.affiliationBorevitz, Justin, College of Medicine, Biology and Environment, CMBE Research School of Biology, Division of Plant Sciences, The Australian National Universityen_AU
local.contributor.affiliationChory, Joanne, Salk Institute for Biological Studies, United States of Americaen_AU
local.contributor.affiliationWeigel, Detlef, Max Planck Institute for Developmental Biology,, Germanyen_AU
local.contributor.authoruidu5264546en_AU
local.description.notesImported from ARIES. At the time of publication, Norman Warthmann was affiliated with the Department of Molecular Biology, Max Planck Institute for Developmental Biology, Tubingen, Germany; Plant Biology Laboratory, The Salk Institute for Biological Sciences, La Jolla, California, United States of America.en_AU
local.identifier.absfor060411en_AU
local.identifier.absseo970106en_AU
local.identifier.ariespublicationf5625xPUB8681en_AU
local.identifier.citationvolume4en_AU
local.identifier.doi10.1371/journal.pone.0004318en_AU
local.identifier.essn1932-6203en_AU
local.identifier.scopusID2-s2.0-84887212422
local.identifier.thomsonID000265483200005
local.publisher.urlhttps://www.plos.org/en_AU
local.type.statusPublished Versionen_AU

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