Quinze ans de « centrale »

Louis Yvert a participé au développement de la « lecture publique », au sein de l’administration centrale de 1968 à 1983. Complétant le témoignage d’Alice Garrigoux sur le Service de la lecture publique (SLP, Éducation nationale, jusqu’en 1975), il évoque dans cet entretien les actions auxquelles il a participé durant cette période, puis à la tête du Service des bibliothèques publiques (SBP, Culture, après 1975)

How does evolution tune biological noise?

International audiencePart of molecular and phenotypic differences between individual cells, between body parts, or between individuals can result from biological noise. This source of variation is becoming more and more apparent thanks to the recent advances in dynamic imaging and single-cell analysis. Some of these studies showed that the link between genotype and phenotype is not strictly deterministic. Mutations can change various statistical properties of a biochemical reaction, and thereby the probability of a trait outcome. The fact that they can modulate phenotypic noise brings up an intriguing question: how may selection act on these mutations? In this review, we approach this question by first covering the evidence that biological noise is under genetic control and therefore a substrate for evolution. We then sequentially inspect the possibilities of negative, neutral, and positive selection for mutations increasing biological noise. Finally, we hypothesize on the specific case of H2A.Z, which was shown to both buffer phenotypic noise and modulate transcriptional efficiency. The recent advances in dynamic imaging and single-cell studies have revealed the stochastic nature of biochemical reactions. Numerous factors are known to affect the degree of noise in these reactions, including temperature (Jo et al., 2005), drug treatment (Dar et al., 2014), age (Bahar et al., 2006) and, very importantly, genotypes (Raser and O'Shea, 2004; Levy and Siegal, 2008; Ansel et al., 2008; Hornung et al., 2012). If mutations can modulate a reaction without necessarily changing the average concentration of its product, then they do not fit in the traditional (often deterministic) view of genotype–phenotype control. Such mutations can change the probabilistic laws of single-cell traits, such as phenotypic noise, which may have important consequences at the multicellular level (Yvert, 2014). Noise has the property to increase disorder. In contrast, living systems are highly organized, developmental processes are under many constrains, and numerous phenotypic traits display robustness to stochastic variation. It is therefore unclear how optimization and control of noise can affect both fidelity and diversity. One way to apprehend this is to examine the mutations that were shown to increase or decrease noise levels. In this review, we first present evidence that noise is under genetic control. We then speculate on the ways by which natural selection acts on it. Finally, we hypothesize on the contribution of histone variant H2A.Z to noise evolution

Genetic Complexity and Quantitative Trait Loci Mapping of Yeast Morphological Traits

Functional genomics relies on two essential parameters: the sensitivity of phenotypic measures and the power to detect genomic perturbations that cause phenotypic variations. In model organisms, two types of perturbations are widely used. Artificial mutations can be introduced in virtually any gene and allow the systematic analysis of gene function via mutants fitness. Alternatively, natural genetic variations can be associated to particular phenotypes via genetic mapping. However, the access to genome manipulation and breeding provided by model organisms is sometimes counterbalanced by phenotyping limitations. Here we investigated the natural genetic diversity of Saccharomyces cerevisiae cellular morphology using a very sensitive high-throughput imaging platform. We quantified 501 morphological parameters in over 50,000 yeast cells from a cross between two wild-type divergent backgrounds. Extensive morphological differences were found between these backgrounds. The genetic architecture of the traits was complex, with evidence of both epistasis and transgressive segregation. We mapped quantitative trait loci (QTL) for 67 traits and discovered 364 correlations between traits segregation and inheritance of gene expression levels. We validated one QTL by the replacement of a single base in the genome. This study illustrates the natural diversity and complexity of cellular traits among natural yeast strains and provides an ideal framework for a genetical genomics dissection of multiple traits. Our results did not overlap with results previously obtained from systematic deletion strains, showing that both approaches are necessary for the functional exploration of genomes

Evaluation de la réorganisation cérébrale du langage chez les patients épileptiques. Apport de la psychologie cognitive

National audienceL'objectif de cet article est de rappeler les exigences spécifiques nécessaires à la mise en place d'un paradigme d'activation en IRMf dans le cadre de l'évaluation fonctionnelle du langage lors du bilan pré- et post-chirurgical de l'épilepsie