Recent publications

Floriot S, Bellutti L, Castille J, Moison P, Messiaen S, Passet B, Boulanger L, Boukadiri A, Tourpin S, Beauvallet C, Vilotte M, Riviere J, Pechoux C, Bertaud M, Vilotte JL, Livera G. 2022. CEP250 is Required for Maintaining Centrosome Cohesion in the Germline and Fertility in Male Mice. Front Cell Dev. 

Magnier J, Druet T, Naves M, Ouvrard M, Raoul S, Janelle J, Moazami-Goudarzi K, Lesnoff M, Tillard E, Gautier M, Flori L. 2022. The genetic history of Mayotte and Madagascar cattle breeds mirrors the complex pattern of human exchanges in Western Indian Ocean. G3. 

Rau A, Passet B, Castille J, Daniel-Carlier N, Asset A, Lecardonnel J, Moroldo M, Jaffrézic F, Laloë D, Moazami-Goudarzi K, Vilotte JL. 2022. Potential genetic robustness of Prnp and Sprn double knockout mouse embryos towards ShRNA-lentiviral inoculation. Vet Res. 

2021

Boufroura FZ, Tomkiewicz‑Raulet C, Poindessous V, Castille J, Vilotte JL,  Bastin J, Mouillet‑Richard S, Djouadi F. 2021. Cellular prion protein dysfunction in a prototypical inherited metabolic myopathy. Cell Mol Life Sci. ahead of print. 

Castille J, Passet B, Makhzami S, Vilotte M, Moazami-Goudarzi K, Truchet S, Daniel-Carlier N, Gaillard AL, Andréoletti O, Vaiman D, Beauvallet C, Vaiman A, Floriot S, Calvel P, Mouillet-Richard S, Duchesne A, Béringue V, Vilotte JL. 2021. Co-invalidation of Prnp and Sprn in FVB/N mice affects reproductive performances and highlight complex biological relationship between PrP and Shadoo. Biochem Biophys Res Commun. 551.

Chadourne M, Poumerol E, Jouneau L, Passet B, Castille J, Sellem E, Pailhoux E, Mandon-Pepin B. 2021. Structural and Functional Characterization of a Testicular Long Non-coding RNA (4930463O16Rik) Identified in the Meiotic Arrest of the Mouse Topaz1(-/-) Testes. Front Cell Dev Biol. 9

Douet JY, Huor A, Cassard H, Lugan S, Aron N, Mesic C, Vilette D, Barrio T, Streichenberger N, Perret-Liaudet A, Delisle MB, Peran P, Deslys JP, Comoy E, Vilotte JL, Goudarzi K, Beringue V, Barria MA, Ritchie DL, Ironside JW, Andreoletti O. 2021. Prion strains associated with iatrogenic CJD in French and UK human growth hormone recipients. Acta Neuropath Com, 9

Floriot S, Duchesne D, Grohs C, Hozé C, Deloche MC, Fayolle G, Vilotte JL, Boichard D, Fritz S,  Boussaha M. 2021. A missense mutation in the FZD7 gene is associated with dilution of the red areas of the coat in Montbéliarde cattle. Anim Genet.

Malkmus J, Martins LR, Jhanwar S, Kircher B, Palacio V, Sheth R, Leal F, Duchesne A, Lopez-Rios J, Peterson KA, Reinhardt R, Onimaru K, Cohn MJ, Zuniga A, Zeller R. 2021. Spatial regulation by multiple Gremlin1 enhancers provides digit development with cis-regulatory robustness and evolutionary plasticity. Nature Comm. 12 

Moazami-Goudarzi K, Andreoletti O, Vilotte JL, Beringue V. 2021. Review on PRNP genetics and susceptibility to chronic wasting disease of Cervidae. Vet Research. 128

2020

Bagheri-Fam S, Chen, HJ, Wilson S, Ayers K, Hughes J,  Sloan-Bena F, Calvel P, Robevska G, Puisac B, Kusz-Zamelczyk K, Gimelli S, Spik A, Jaruzelska J, Warenik-Szymankiewicz A, Faradz S, Nef S, Pie J, Thomas P, Sinclair A, Wilhelm D. 2020. The gene encoding the ketogenic enzyme HMGCS2 displays a unique expression during gonad development in mice. PLoS One. 15, e0227411

Béringue V, Tixador P, Andréoletti O, Reine F, Castille J, Laï TL, Le Dur A, Laisné A, Herzog L, Passet B, Rezaei H, Vilotte JL, Laude H. 2020. Host prion protein expression levels impact prion tropism for the spleen. PLoS Pathog. 16, e1008283

Bignon Y, Poindessous V, Lazareth H, Passet B, Vilotte JL, Djouadi F, Mouillet-Richard S, Pallet N. 2020. The cellular prion protein is a stress protein secreted by renal tubular cells and a urinary marker of kidney injury. Cell Death Dis. 11, 243

Ducat A, Couderc B, Bouter A, Biquard L, Aouache R, Passet B, Doridot L, Cohen MB, Ribaux P, Apicella C, Gaillard I, Palfray S, Chen Y, Vargas A, Julé A, Frelin L, Cocquet J, San Martin CR, Jacques S, Busato F, Tost J, Méhats C, Laissue P, Vilotte JL, Miralles F, Vaiman D. 2020. Molecular mechanisms of trophoblast dysfunction mediated by imbalance between STOX1 isoforms. Science. 23, 101086

Grau ET, Charles M, Femenia M, Rebours E, Vaiman A, Rocha D. 2020. Survey of mitochondrial sequences integrated into the bovine nuclear genome. Sci Rep. 10, 2077

Moudjou M, Castille J, Passet B, Herzog L, Reine F, Vilotte JL, Rezaei H, Béringue V, Igel-Egalon A. 2020. Improving the predictive value of prion inactivation validation methods to minimize the risks of iatrogenic transmission with medical instruments. Front Bioeng Biotechnol, 8, 591024

Passet B, Castille J, Makhzami S, Truchet S, Vaiman A, Floriot S,  Moazami-Goudarzi K, Vilotte M, Gaillard AL, Helary L, Bertaud M, Andréoletti O, Vaiman D, Calvel P, Daniel-Carlier N, Moudjou M, Beauvallet C, Benharouga M, Laloë D, Mouillet-Richard S, Duchesne A, Béringue V, Vilotte JL. 2020. The Prion-like protein Shadoo is involved in mouse embryonic and mammary development and differentiation. Sci Rep, 10-6765

Tramontin Grau E, Charles M, Féménia  M, Rebours E, Vaiman A, Rocha D. 2020. Survey of mitochondrial sequences integrated into the bovine nuclear genome. Sci Rep. 10, 2077

2019

Boushaba N, Boujenane I, Moazami-Goudarzi K, Flori L, Saïdi-Mehtar N, Tabet-Aoul N, Laloë D. 2019. Genetic diversity and relationships among six local cattle populations in semi-arid areas assessed by a bovine medium-density single nucleotide polymorphism data. Animal. 13, 8-14. 

Ducat A, Vargas A Doridot L, Bagattin A, Lerner J, Vilotte JL, Buffat C, Pontoglio M, Miralles F, Vaiman D. 2019. Low-dose aspirin protective effects are correlated with deregulation of HNF factor expression in the preeclamptic placentas from mice and humans. Cell Death Discov. 5, 94

Erlandsson L, Ducat A, Castille J, Zia I, Kalapotharakos G, Hedstrom E, Vilotte JL, Vaiman D, Hansson SR. 2019. Alpha-1 microglobulin as a potential therapeutic candidate for treatment of hypertension and oxidative stress in the STOX1 preeclampsia mouse model. Sci Rep. 9, 8561

Fares-Taie LF, Nedelec B, David P, Angee C, Crippa S, Passet B, Vilotte J, Chassaing N, Kaplan J, Kostic C, Calvas P, Rozet J. 2019. Submicroscopic 13q32.1 deletions causing congenital microcoria modify the regulatory landscape of neighboring genes by enhancer adoption. Eur J Hum Genet. 96, 631-639

Flori L, Moazami-Goudarzi K, Alary V, Araba A, Boujenane I, Boushaba N, Casabianca F, Casu S, Ciampolini R, Coeur D'acier A, Coquelle C, Delgado JV, El-Beltagi A, Hadjipavlou G, Jousselin E, Landi V, Lauvie A, Lecomte P, Ligda C, Marinthe C, Martinez A, Mastrangelo S, Menni D, Moulin CH, Osman MA, Pineau O, Portolano B, Rodellar C, Saidi-Mehtar N, Sechi T, Sempere G, Thevenon S, Tsiokos D, Laloë D, Gautier M. 2019. A genomic map of climate adaptation in Mediterranean cattle breeds. Mol Ecol. 28, 1009-1029

Gobé C, El Zaiat M, Meunier N, André M, Sellem E, Congar P, Jouneau L, Allais-Bonnet A, Naciri I, Passet B, Pailhoux E, Pannetier M. 2019. Dual role of DMXL2 in olfactory information transmission and the first wave of spermatogenesis. PLoS Genet. 15,  e1007909

Helary L, Castille J, Passet B, Vaiman A, Beauvallet C, Jaffrezic F, Charles M, Tamzini M, Baraige F, Letheule M, Laubier J, Moazami-Goudarzi K, Vilotte JL, Blanquet V, Duchesne A. DNAJC2 is required for mouse early embryonic development. Biochem Biophys Res Commun. 516, 258-263

Hirsch TZ, Martin-Lanneree S, Reine , Hernandez-Rapp J, Herzog L, Dron M, Privat N, Passet B, Halliez S, Villa-Diaz A, Lacroux C, Klein V, Haik S, Andreoletti O, Torres JM, Vilotte JL, Beringue V, Mouillet-Richard S. 2019. Epigenetic control of the Notch and Eph signaling pathways by the prion protein: implications for prion diseases.  Mol Neurobiol. 56, 2159-2173

Le Guillou S, Laubier J, Pechoux C, Aujean E, Castille J, Leroux C, Le Provost F. 2019. Defects of the endoplasmic reticulum and changes to lipid droplet size in mammary epithelial cells due to miR-30b-5p overexpression are correlated to a reduction in Atlastin 2 expression. Biochem Biophys Res Commun. 512, 283-288

Vilotte JL, Pailhoux E. 2019. Intérêts des techniques de modifications ciblées du génome («Génome Editing») chez les animaux de rente. Bull Acad Vét Fr. 172, 1-6

2018

Caillot N, Bouley J, Jain M, Mariano S, Luce S, Horiot S, Airouche S, Beuraud C, Beauvallet C, Devillier P, Chollet-Martin S, Kellenberger,  C, Mascarell L, Chabre H, Batard T, Nony E, Lombardi V, Baron-Bodo V, Moingeon P. 2017. Sialylated Fetuin-A as a candidate predictive biomarker for successful grass pollen allergen immunotherapy. J Allergy Clin Immunol. 140, 759-770.

Dewaele A, Persuy MA, Badonnel K, Meunier N, Durieux D, Castille J, Favreau-Peigne A, Baly C. 2018. Chronic perinatal odour exposure with heptaldehyde affects odour sensitivity and olfactory system homeostasis in preweaning mice. Behav Brain Res. 347, 414-424

Duchesne A, Vaiman A, Castille J, Beauvallet C, Gaignard P, Floriot S, Rodriguez S, Vilotte M, Boulanger L, Passet B, Albaric O, Guillaume F, Boukadiri A, Richard L, Bertaud M, Timsit E, Guatteo R, Jaffrézic F, Calvel P, Helary L, Mahla R, Esquerré D, Péchoux C, Liuu S, Vallat JM, Boichard D, Slama A, Vilotte JL. 2017. Bovine and murine models highlight novel roles for SLC25A46 in mitochondrial dynamics and metabolism, with implications for human and animal health. PLoS Genet. 13, e1006597

Gilbert H, Billon Y, Brossard L, Faure J, Gatellier P, Gondret F, Labussière E, Lebret B, Lefaucheur L, Le Floch N, Louveau I, Merlot E, Meunier-Salaün MC, Montagne L, Mormede P, Renaudeau D, Riquet J, Rogel-Gaillard C, van Milgen J, Vincent A, Noblet J. 2017. Review: divergent selection for residual feed intake in the growing pig. Animal. ahead of printMartin-Lannerée S, Halliez S, Hirsch TZ, Hernandez-Rapp J, Passet B, Tomkiewicz C, Villa-Diaz A, Torres JM, Launay JM, Béringue V, Vilotte JL, Mouillet-Richard S. 2017. The cellular prion protein controls notch signaling in neural stem/progenitor cells. Stem Cells. 35, 754-795

Ilaslan E, Calvel P, Nowak D, Szarras-Czapnik M, Slowikowska-Hilczer J, Spik A, Sararols P, Nef S, Jaruzelska J, Kusz-Zamelczyk K. 2018. A case of two sisters suffering from 46,XY gonadal dysgenesis and carrying a mutation of a novel candidate sex-determining Gene STARD8 on the X chromosome. Sex Dev. 12, 191-195

Le Dur A, Lan Laı T, Stinnakre MG, Laisne A, Chenais N, Rakotobe S, Passet B, Reine F, Soulier S, Herzog L, Tilly G, Rezaei H, Beringue V, Vilotte JL, Laude H. 2017.  Divergent prion strain evolution driven by PrPC expression level in transgenic mice. Nat Comm. 8, 14170

Neirijnck Y, Calvel P, Kilcoyne KR, Kühne F, Stévant I, Griffeth RJ, Pitetti JL, Andric SA, Hu MC, Pralong F, Smith LB, Nef S. 2018. Insulin and IGF1 receptors are essential for the development and steroidogenic function of adult Leydig cells. FASEB J. 32, 3321-3335

2016

Allais-Bonnet A, Castille J, Pannetier M, Passet B, Elzaiat M, Andre M, Montazer-Torbati F, Moazami-Goudarzi K, Vilotte JL, Pailhoux E. 2016. A specific role for PRND in goat foetal Leydig cells is suggested by prion family gene expression during gonad development in goats and mice.  Febs Open Bio. 6, 4-156

Ducat A, Doridot L, Calicchio R, Méhats C, Vilotte JL, Castille J, Barbaux S, Couderc B, Jacques S, Letourneur F, Buffat C, Le Grand F, Laissue P, Miralles F, Vaiman D. 2016. Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia. Sci Rep. 6, 19196

Duchesne A, Grohs C, Michot P, Bertaud M, Boichard D, Floriot S, Capitan A. 2016. Du phénotype à la mutation causale : le cas des anomalies récessives bovines. Inra Prod Anim. 29, 319-328      

Gautier M, Moazami-Goudarzi K, Leveziel H, Grohs C, Rialle S, Kowalczyk R, Flori L . 2016. Deciphering the Wisent demographic and adaptive histories from individual whole-genome sequences. Molec Biol Evol. 33, 2801-2814

Grohs C, Duchesne A, Floriot S, Deloche MC, Boichard D, Ducos A, Danchin-Burge C. 2016. L’Observatoire National des Anomalies Bovines, son action et ses résultats pour une aide efficace à la gestion des anomalies génétiques. Inra Prod Anim. 29, 307-318  

Khalifé M, Reine F, Paquet-Fifield S, Castille J, Herzog L, Vilotte M, Moudjou M, Moazami-Goudarzi K, Makhzami S, Passet B, Andréoletti O, Vilette D, Laude H, Béringue V, Vilotte JL. 2016. Mutated but Not Deleted Ovine PrPC N-Terminal Polybasic Region Strongly Interferes with Prion Propagation in Transgenic Mice. J Virol. 90, 1638-1646

Martin-Lannerée S, Halliez S, Hirsch TZ, Hernandez-Rapp J, Passet B, Tomkiewicz C, Villa-Diaz A, Torres JM, Launay JM, Béringue V, Vilotte JL, Mouillet-Richard S. 2016. The cellular prion protein controls Notch signalling in neural stem / progenitor cells. Stem Cells. ahead of print

Previous publications

Daniel-Carlier N, Sawafta A, Passet B, Thépot D, Leroux-Coyau M, Lefèvre F, Houdebine LM, Jolivet G. 2013. Viral infection resistance conferred on mice by siRNA transgenesis. Transgenic Res. 22, 489-500

Doridot L, Châtre L, Ducat A, Vilotte JL, Lombès A, Méhats C, Barbaux S, Calicchio R, Ricchetti M, Vaiman D. 2014. Nitroso-redox balance and mitochondrial homeostasis are regulated by STOX1, a pre-eclampsia-associated gene. Antioxid Redox Signal. 21, 819-834

Doridot L., Passet B., Mehats C., Rigourd V., Barbaux S., Ducat A., Mondon F., Vilotte M., Castille J., Breuiller-Fouche M., Daniel N., le Provost F., Bauchet A.L., Baudrie V., Hertig A., Buffat C., Simeoni U., Germain G., Vilotte J.L., Vaiman D. 2013. Preeclampsia-Like Symptoms Induced in Mice by Fetoplacental Expression of STOX1 Are Reversed by Aspirin Treatment. Hypertension 61,662-668

Fares-Taie L, Gerber S, Tawara A, Ramirez-Miranda A, Douet JY, Verdin H, Guilloux A, Zenteno JC, Kondo H, Moisset H, Passet B, Yamamoto K, Iwai M, Tanaka T, Nakamura Y, Kimura W, Bole-Feysot C, Vilotte M, Odent S, Vilotte JL, Munnich A, Regnier A, Chassaing N, De Baere E, Raymond-Letron I, Kaplan J, Calvas P, Roche O, Rozet JM. 2015. Submicroscopic deletions at 13q32.1 cause congenital microcoria. Am J Hum Genet. 96, 631- 639

Flori L, Thevenon S, Dayo G-K,Senou M, Sylla S, Berthier D, Moazami-Goudarzi K, Gautier M. 2014. Adaptative admixture in the west African bovine hybrid zone insight from the borgou population. Mol Ecol . 23, 3241-3257

Floriot S, Vesque C, Rodriguez S, Bourgain-Guglielmetti F, Karaiskou A, Gautier M, Duchesne A, Barbey S, Fritz S, Vasilescu A, Bertaud M, Moudjou M, Halliez S, Cormier-Daire V, El Hokayem J, Nigg EA, Manciaux L, Guatteo R, Cesbron N, Toutirais G, Eggen A, Schneider-Maunoury S, Boichard D, Sobczak-Thépot J, Schibler L. 2015. C-Nap1 mutation affects centriole cohesion and is associated with a Seckel-like syndrome in cattle. Nat Commun. 6, 6894

Halliez S, Chesnais N, Mallucci G, Vilotte M, Langevin C, Jaumain E, Laude H, Vilotte JL, Beringue V. 2013. Targeted knock-down of cellular prion protein expression in myelinating Schwann cells does not alter mouse prion pathogenesis. J Gen Virol. 94, 1435-1440

Halliez S, Martin-Lanneree S, Passet B, Hernandez-Rapp J, Castille J, Urien C, Chat S, Laude H, Vilotte JL, Mouillet-Richard S, Beringue V. 2015. Prion protein localizes at the ciliary base during neural and cardiovascular development, and its depletion affects α-tubulin post-translational modifications. Sci Rep. 5, 17146

Halliez S, Passet B, Martin-Lannerée S, Hernandez-Rapp J, Laude H, Mouillet-Richard S, Vilotte JL, Béringue V. To develop with or without the prion protein. Front Cell Dev Biol. 2, 58

Halliez S, Reine F, Herzog L, Jaumain E, Haïk S, Rezaei H, Vilotte JL, Laude H, Béringue V. 2014. Accelerated, spleen-based titration of variant Creutzfeldt-Jakob disease infectivity in transgenic mice expressing human prion protein with sensitivity comparable to that of survival time bioassay. J Virol. 88, 8678- 8686

Jolivet G, Braud S, DaSilva B, Passet B, Harscoët E, Viglietta C, Gautier T, Lagrost L, Daniel-Carlier N, Houdebine LM, Harosh I. 2014. Induction of body weight loss through RNAi-knockdown of APOBEC1 gene expression in transgenic rabbits. PLoS ONE. 9, e106655

Lopez-Rios J, Duchesne A, Speziale D, Andrey G, Peterson KA, German P, Ünal E, Liu J, Floriot S, Barbey S, Gallard Y, Müller-Gerbl M, Courtney AD, Klopp C, Rodriguez S, Ivanek R, Beisel C, Wicking C, Iber D, Robert B, McMahon AP, Duboule D, Zeller R. 2014. Attenuated sensing of SHH by Ptch1underlies evolution of bovine limbs. Nature.  511, 46-51

Makzhami S, Passet B, Halliez S, Castille J, Moazami-Goudarzi K, Duchesne A, Vilotte M, Laude H, Mouillet-Richard S, Béringue V, Vaiman D, Vilotte JL. 2014. The prion protein family: a view from the placenta. Front Cell Dev Biol. 2, 35

Martin-Lannerée S, Hirsch TZ, Hernandez-Rapp J, Halliez S, Vilotte JL, Launay JM, Mouillet-Richard S. 2014. PrP(C) from stem cells to cancer. Front Cell Dev Biol. 2, 55

Mouillet-Ricard S, Vilotte JL. 2015. Promiscuous functions of the prion protein family. Front Cell Dev Biol. 3, 7

Passet B, Halliez S, Béringue V, Laude H, Vilotte JL.  2013. The prion protein family: Looking outside the central nervous system. Prion 7, 127-130

Sarradin P, Viglietta C, Limouzin C, Andreoletti O, Daniel-Carlier N, Barc C, Leroux-Coyau M, Berthon P, Chapuis J, Rossignol C, Gatti JL, Belghazi,M, Labas V, Vilotte JL, Beringue V, Lantier F, Laude H, Houdebine LM. 2015. Transgenic Rabbits Expressing Ovine PrP Are Susceptible to Scrapie. PLoS Pathogens. 11, e1005077

Wangkumhang P, Wilantho A, Shaw PJ, Flori L, Moazami-Goudarzi K, Gautier M, Duangjinda M, Assawamakin A, Tongsima S. 2015. Genetic analysis of Thai cattle reveals a Southeast Asian indicine ancestry. Peer J. 3, e1318