A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse

Curly horses present a variety of curl phenotypes that are associated with various degrees of curliness of coat, mane, tail and ear hairs. Their origin is still a matter of debate and several genetic hypotheses have been formulated to explain the diversity in phenotype, including the combination of autosomal dominant and recessive alleles. Our purpose was to map the autosomal dominant curly hair locus and identify the causal variant using genome-wide association study (GWAS) and whole-genome sequencing approaches. A GWAS was performed using a Bayesian sparse linear mixed model, based on 51 curly and 19 straighthaired French and North American horses from 13 paternal families genotyped on the Illumina EquineSNP50 Bead-Chip. A single strong signal was observed on equine chromosome 11, in a region that encompasses the type I keratin gene cluster. This region was refined by haplotype analysis to a segment including 36 genes, among which are 10 keratin genes (KRT-10, -12, -20, -23, -24, -25, -26, -27, -28, -222). To comprehensively identify candidate causal variants within all these genes, whole-genome sequences were obtained for one heterozygous curly stallion and its straighthaired son. Among the four non-synonymous candidate variants identified and validated in the curly region, only variant g. 21891160G> A in the KRT25 gene (KRT25:p.R89H) was in perfect agreement with haplotype status in the whole pedigree. Genetic association was then confirmed by genotyping a larger population consisting of 353 horses. However, five discordant curly horses were observed, which carried neither the variant nor the main haplotype associated with curliness. Sequencing of KRT25 for two discordant horses did not identify any other deleterious variant, which suggests locus rather than allelic heterogeneity for the curly phenotype. We identified the KRT25: p. R89H variant as responsible for the dominant curly trait, but a second dominant locus may also be involved in the shape of hairs within North American Curly horses

Omics technologies provide new insights into the molecular physiopathology of equine osteochondrosis

Background: Osteochondrosis (OC(D)) is a juvenile osteo-articular disorder affecting several mammalian species. In horses, OC(D) is considered as a multifactorial disease and has been described as a focal disruption of endochondral ossification leading to the development of osteoarticular lesions. Nevertheless, OC(D) physiopathology is poorly understood. Affected horses may present joint swelling, stiffness and lameness. Thus, OC(D) is a major concern for the equine industry. Our study was designed as an integrative approach using omics technologies for the identification of constitutive defects in epiphyseal cartilage and/or subchondral bone associated with the development of primary lesions to further understand OC(D) pathology. This study compared samples from non-affected joints (hence lesion-free) from OC(D)-affected foals (n = 5, considered predisposed samples) with samples from OC-free foals (n = 5) considered as control samples. Consequently, results are not confounded by changes associated with the evolution of the lesion, but focus on altered constitutive molecular mechanisms. Comparative proteomics and micro computed tomography analyses were performed on predisposed and OC-free bone and cartilage samples. Metabolomics was also performed on synovial fluid from OC-free, OC(D)-affected and predisposed joints. Results: Two lesion subtypes were identified: OCD (lesion with fragment) and OC (osteochondral defects). Modulated proteins were identified using omics technologies (2-DE proteomics) in cartilage and bone from affected foals compare to OC-free foals. These were associated with cellular processes including cell cycle, energy production, cell signaling and adhesion as well as tissue-specific processes such as chondrocyte maturation, extracellular matrix and mineral metabolism. Of these, five had already been identified in synovial fluid of OC-affected foals: ACTG1 (actin, gamma 1), albumin, haptoglobin, FBG (fibrinogen beta chain) and C4BPA (complement component 4 binding protein, alpha). Conclusion: This study suggests that OCD lesions may result from a cartilage defect whereas OC lesions may be triggered by both bone and cartilage defects, suggesting that different molecular mechanisms responsible for the equine osteochondrosis lesion subtypes and predisposition could be due to a defect in both bone and cartilage. This study will contribute to refining the definition of OC(D) lesions and may improve diagnosis and development of therapies for horses and other species, including humans

LIPH Expression in Skin and Hair Follicles of Normal Coat and Rex Rabbits

Natural mutations in the LIPH gene were shown to be responsible for hair growth defects in humans and for the rex short hair phenotype in rabbits. In this species, we identified a single nucleotide deletion in LIPH (1362delA) introducing a stop codon in the C-terminal region of the protein. We investigated the expression of LIPH between normal coat and rex rabbits during critical fetal stages of hair follicle genesis, in adults and during hair follicle cycles. Transcripts were three times less expressed in both fetal and adult stages of the rex rabbits than in normal rabbits. In addition, the hair growth cycle phases affected the regulation of the transcription level in the normal and mutant phenotypes differently. LIPH mRNA and protein levels were higher in the outer root sheath (ORS) than in the inner root sheath (IRS), with a very weak signal in the IRS of rex rabbits. In vitro transfection shows that the mutant protein has a reduced lipase activity compared to the wild type form. Our results contribute to the characterization of the LIPH mode of action and confirm the crucial role of LIPH in hair production

A Deletion in Exon 9 of the LIPH Gene Is Responsible for the Rex Hair Coat Phenotype in Rabbits (Oryctolagus cuniculus)

The fur of common rabbits is constituted of 3 types of hair differing in length and diameter while that of rex animals is essentially made up of amazingly soft down-hair. Rex short hair coat phenotypes in rabbits were shown to be controlled by three distinct loci. We focused on the “r1” mutation which segregates at a simple autosomal-recessive locus in our rabbit strains. A positional candidate gene approach was used to identify the rex gene and the corresponding mutation. The gene was primo-localized within a 40 cM region on rabbit chromosome 14 by genome scanning families of 187 rabbits in an experimental mating scheme. Then, fine mapping refined the region to 0.5 cM (Z = 78) by genotyping an additional 359 offspring for 94 microsatellites present or newly generated within the first defined interval. Comparative mapping pointed out a candidate gene in this 700 kb region, namely LIPH (Lipase Member H). In humans, several mutations in this major gene cause alopecia, hair loss phenotypes. The rabbit gene structure was established and a deletion of a single nucleotide was found in LIPH exon 9 of rex rabbits (1362delA). This mutation results in a frameshift and introduces a premature stop codon potentially shortening the protein by 19 amino acids. The association between this deletion and the rex phenotype was complete, as determined by its presence in our rabbit families and among a panel of 60 rex and its absence in all 60 non-rex rabbits. This strongly suggests that this deletion, in a homozygous state, is responsible for the rex phenotype in rabbits

A Deletion in Exon 9 of the LIPH Gene Is Responsible for the Rex Hair Coat Phenotype in Rabbits (Oryctolagus cuniculus)

The fur of common rabbits is constituted of 3 types of hair differing in length and diameter while that of rex animals is essentially made up of amazingly soft down-hair. Rex short hair coat phenotypes in rabbits were shown to be controlled by three distinct loci. We focused on the “r1” mutation which segregates at a simple autosomal-recessive locus in our rabbit strains. A positional candidate gene approach was used to identify the rex gene and the corresponding mutation. The gene was primo-localized within a 40 cM region on rabbit chromosome 14 by genome scanning families of 187 rabbits in an experimental mating scheme. Then, fine mapping refined the region to 0.5 cM (Z = 78) by genotyping an additional 359 offspring for 94 microsatellites present or newly generated within the first defined interval. Comparative mapping pointed out a candidate gene in this 700 kb region, namely LIPH (Lipase Member H). In humans, several mutations in this major gene cause alopecia, hair loss phenotypes. The rabbit gene structure was established and a deletion of a single nucleotide was found in LIPH exon 9 of rex rabbits (1362delA). This mutation results in a frameshift and introduces a premature stop codon potentially shortening the protein by 19 amino acids. The association between this deletion and the rex phenotype was complete, as determined by its presence in our rabbit families and among a panel of 60 rex and its absence in all 60 non-rex rabbits. This strongly suggests that this deletion, in a homozygous state, is responsible for the rex phenotype in rabbits

Multiscale energy budget of inertially driven turbulence in normal and superfluid helium

20 pages, 15 figures, submitted to Peer journalInternational audienceIn this paper we present a novel hydrodynamic experiment using liquid $^4$He.Lagrangian trajectories are obtained using two-domensional particle trackingon hollow glass microspheres in a cryogenic liquid helium turbulent flow.The flow is forced inertially by a canonical oscillating grid, both belowand above the superfluid transition. This allows for a direct comparison ofthe Lagrangian statistics in the normal (He I), and superfluid (He II) phase.The high temporal resolution allows us to resolve the velocity fluctuations atintegral and inertial scales, and most importantly assess the noisecontribution.The careful analysis of velocity fluctuations, acceleration fluctuations,and pair dispersion, allows us to extract estimates of the energy injectionrate at large scale, the energy flux cascading through inertial scales,and the dissipation rate at small scale, and therefore build the energybudget in both the normal and superfluid phase.We find that, within experimental uncertainty, the statistical features ofturbulence and the energy budget in superfluid helium is indistinguishablefrom those of normal helium, highlighting the importance of conductingexperiments in both He I and He II to draw meaningful conclusions,because deviations from the theoretical predictions may arise from noisecontributions or deviation from the homogeneous and isotropic approximations

Local velocity measurements in the Shrek experiment at high reynolds number

International audienceWe report preliminary results obtained using new local velocity probes in the Superfluid Helium high REynold number von Kármán flow (SHREK) experiment for different forcing conditions. The presentation will focus on the validation of the signals obtained from a hot-wire and a total head pressure tube in both normal and superfluid phases of liquid helium

LES APPORTS DE LA GÉNOMIQUE À L’AGROÉCOLOGIE. Bilan des projets financés sur la période 2005 – 2019 et perspectives pour la recherche.

LES « CAHIERS DE L’ANR » traitent de questions thématiques transverses aux différents appels à projets financés par l’ANR. Cette collection, qui existe depuis 2009, met en perspective les recherches, les innovations et les avancées technologiquesen cours dans un domaine spécifique. Sans prétention d’exhaustivité, son objectif est de revenir sur les enjeux sociétaux et les défis d’avenir identifiés par les communautés de recherche mobilisées sur une thématique. Les projets de recherche financés par l’ANR y sont synthétiquement présentés. Chaque cahier s’adresse aux chercheurs, aux décideurs politiques mais aussi au grand public.Le présent cahier (n°12) est le résultat d’une collaboration précieuse entre scientifiques issus des disciplines de la génomique et de l’agroécologie dans le domaine animal, microbien et végétal

LES APPORTS DE LA GÉNOMIQUE À L’AGROÉCOLOGIE. Bilan des projets financés sur la période 2005 – 2019 et perspectives pour la recherche.

LES « CAHIERS DE L’ANR » traitent de questions thématiques transverses aux différents appels à projets financés par l’ANR. Cette collection, qui existe depuis 2009, met en perspective les recherches, les innovations et les avancées technologiquesen cours dans un domaine spécifique. Sans prétention d’exhaustivité, son objectif est de revenir sur les enjeux sociétaux et les défis d’avenir identifiés par les communautés de recherche mobilisées sur une thématique. Les projets de recherche financés par l’ANR y sont synthétiquement présentés. Chaque cahier s’adresse aux chercheurs, aux décideurs politiques mais aussi au grand public.Le présent cahier (n°12) est le résultat d’une collaboration précieuse entre scientifiques issus des disciplines de la génomique et de l’agroécologie dans le domaine animal, microbien et végétal