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Expression variation in connected recombinant populations of Arabidopsis thaliana highlights distinct transcriptome architectures

Overview of attention for article published in BMC Genomics, March 2012
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Title
Expression variation in connected recombinant populations of Arabidopsis thaliana highlights distinct transcriptome architectures
Published in
BMC Genomics, March 2012
DOI 10.1186/1471-2164-13-117
Pubmed ID
Authors

Francisco A Cubillos, Jennifer Yansouni, Hamid Khalili, Sandrine Balzergue, Samira Elftieh, Marie-Laure Martin-Magniette, Yann Serrand, Loïc Lepiniec, Sébastien Baud, Bertrand Dubreucq, Jean-Pierre Renou, Christine Camilleri, Olivier Loudet

Abstract

Expression traits can vary quantitatively between individuals and have a complex inheritance. Identification of the genetics underlying transcript variation can help in the understanding of phenotypic variation due to genetic factors regulating transcript abundance and shed light into divergence patterns. So far, only a limited number of studies have addressed this subject in Arabidopsis, with contrasting results due to dissimilar statistical power. Here, we present the transcriptome architecture in leaf tissue of two RIL sets obtained from a connected-cross design involving 3 commonly used accessions. We also present the transcriptome architecture observed in developing seeds of a third independent cross. The utilisation of the novel R/eqtl package (which goal is to automatize and extend functions from the R/qtl package) allowed us to map 4,290 and 6,534 eQTLs in the Cvi-0 × Col-0 and Bur-0 × Col-0 recombinant populations respectively. In agreement with previous studies, we observed a larger phenotypic variance explained by eQTLs in linkage with the controlled gene (potentially cis-acting), compared to distant loci (acting necessarily indirectly or in trans). Distant eQTLs hotspots were essentially not conserved between crosses, but instead, cross-specific. Accounting for confounding factors using a probabilistic approach (VBQTL) increased the mapping resolution and the number of significant associations. Moreover, using local eQTLs obtained from this approach, we detected evidence for a directional allelic effect in genes with related function, where significantly more eQTLs than expected by chance were up-regulated from one of the accessions. Primary experimental data, analysis parameters, eQTL results and visualisation of LOD score curves presented here are stored and accessible through the QTLstore service database http://qtlstore.versailles.inra.fr/. Our results demonstrate the extensive diversity and moderately conserved eQTL landscape between crosses and validate the utilisation of expression traits to explore for candidates behind phenotypic variation among accessions. Furthermore, this stresses the need for a wider spectrum of diversity to fully understand expression trait variation within a species.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 82 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
France 2 2%
United Kingdom 1 1%
Portugal 1 1%
Netherlands 1 1%
Unknown 77 94%

Demographic breakdown

Readers by professional status Count As %
Researcher 27 33%
Student > Ph. D. Student 10 12%
Student > Master 8 10%
Professor > Associate Professor 6 7%
Professor 5 6%
Other 13 16%
Unknown 13 16%
Readers by discipline Count As %
Agricultural and Biological Sciences 49 60%
Biochemistry, Genetics and Molecular Biology 12 15%
Medicine and Dentistry 5 6%
Computer Science 1 1%
Environmental Science 1 1%
Other 0 0%
Unknown 14 17%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 18 July 2018.
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#16,794,128
of 24,701,594 outputs
Outputs from BMC Genomics
#7,017
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Outputs of similar age
#106,755
of 164,384 outputs
Outputs of similar age from BMC Genomics
#38
of 59 outputs
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