PRDM9 activity depends on HELLS and promotes local 5-hydroxymethylcytosine enrichment.
Imai Y, Biot M, Clément J, Teragaki M, Urbach S, Robert T, Baudat F, Grey C, de Massy B
Méiose et recombinaison
La méiose est une division cellulaire spécialisée qui permet chez les organismes à reproduction sexuée de former des cellules haploïdes à partir de cellules diploïdes. Ceci est réalisé par un cycle cellulaire constitué d’une phase de réplication de l’ADN suivi par deux divisions. La ségrégation réductionnelle des chromosomes lors de la première division de méiose nécessite l’établissement de connections entre chromosomes homologues. Celles-ci sont établies pendant la prophase de la première division par recombinaison homologue qui génère des échanges réciproques, appelés crossing over, entre homologues. L’absence de crossing over conduit le plus souvent à des défauts de ségrégation et à la stérilité. Des altérations du programme de recombinaison peuvent aussi conduire à de l’instabilité génomique et à des aneuploïdies. Par ailleurs, les événements de recombinaison homologues en méiose déterminent les associations génétiques et contribuent à la diversité des génomes et à leur évolution.
Notre equipe s’intéresse à plusieurs aspects du mécanisme moléculaire de la recombinaison méiotique et de ses implications évolutives en utilisant la souris comme système modèle. La recombinaison méiotique est initiée par l’induction programmée de centaines de cassures double brin de l’ADN dont la réparation conduit à la formation de crossing over et conversion géniques. Les principales étapes et facteurs impliqués dans ces processus ont été conservés au cours de l’évolution.
PUBLICATIONS DE L'ÉQUIPE
Reading the epigenetic code for exchanging DNA.
Biot M, de Massy B
Mouse ANKRD31 Regulates Spatiotemporal Patterning of Meiotic Recombination Initiation and Ensures Recombination between X and Y Sex Chromosomes.
Papanikos F, Clément JAJ, Testa E, Ravindranathan R, Grey C, Dereli I, Bondarieva A, Valerio-Cabrera S, Stanzione M, Schleiffer A, Jansa P, Lustyk D, Fei JF, Adams IR, Forejt J, Barchi M, de Massy B, Toth A
Sex chromosome quadrivalents in oocytes of the African pygmy mouse Mus minutoides that harbors non-conventional sex chromosomes.
Baudat F, de Massy B, Veyrunes F
Mouse REC114 is essential for meiotic DNA double-strand break formation and forms a complex with MEI4.
Kumar R, Oliver C, Brun C, Juarez-Martinez AB, Tarabay Y, Kadlec J, de Massy B
PRDM9, a driver of the genetic map.
Grey C, Baudat F, de Massy B
PRDM9 Methyltransferase Activity Is Essential for Meiotic DNA Double-Strand Break Formation at Its Binding Sites.
Diagouraga B, Clément JAJ, Duret L, Kadlec J, de Massy B, Baudat F
In vivo binding of PRDM9 reveals interactions with noncanonical genomic sites
Grey C, Clément JA, Buard J, Leblanc B, Gut I, Gut M, Duret L, de Massy B.
The PRDM9 KRAB domain is required for meiosis and involved in protein interactions
Imai Y, Baudat F, Taillepierre M, Stanzione M, Toth A, de Massy B.
TopoVIL : a molecular scissor essential for reproduction
Robert, T, De Massy, B, Grelon, M.
Birth and death of a protein
Clément J, de Massy B
SKAP, an outer kinetochore protein, is required for mouse germ cell development
Grey C, Espeut J, Ametsitsi R, Kumar R, Luksza M, Brun C, Verlhac MH, Suja JÁ, de Massy B
The TopoVIB-Like protein family is required for meiotic DNA double-strand break formation
Robert T, Nore A, Brun C, Maffre C, Crimi B, Bourbon HM, de Massy B
A new light on the meiotic DSB catalytic complex
Robert T, Vrielynck N, Mézard C, de Massy B, Grelon M
Meiotic DNA break formation requires the unsynapsed chromosome axis-binding protein IHO1 (CCDC36) in mice
Stanzione M, Baumann M, Papanikos F, Dereli I, Lange J, Ramlal A, Tränkner D, Shibuya H, de Massy B, Watanabe Y, Jasin M, Keeney S, Tóth A
MEI4: a central player in the regulation of meiotic DNA double strand break formation in the mouse
Kumar R, Ghyselinck N, Ishiguro KI, Watanabe Y, Kouznetsova A, Höög C, Strong E, Schimenti J, Daniel K, Toth A, de Massy B.
Meiosis: early DNA double-strand breaks pave the way for inter-homolog repair
Borde V, de Massy B
Diversity of Prdm9 Zinc Finger Array in Wild Mice Unravels New Facets of the Evolutionary Turnover of this Coding Minisatellite
Buard J, Rivals E, Dunoyer de Segonzac D, Garres C, Caminade P, de Massy B, Boursot P.
Mouse tetrad analysis provides insights into recombination mechanisms and hotspot evolutionary dynamics
Cole F, Baudat F, Grey C, Keeney S, de Massy B, Jasin M.
Human genetics. Hidden features of human hotspots
de Massy B.
Spp1 links sites of meiotic DNA double-strand breaks to chromosome axes
De Massy, B.
Programmed induction of DNA double strand breaks during meiosis: setting up communication between DNA and the chromosome structure.
Borde V, de Massy B.
RNF212 is a dosage-sensitive regulator of crossing-over during mammalian meiosis
Reynolds A, Qiao H, Yang Y, Chen JK, Jackson N, Biswas K, Holloway JK, Baudat F, de Massy B, Wang J, Höög C, Cohen PE, Hunter N.
Drosophila Yemanuclein and HIRA Cooperate for De Novo Assembly of H3.3-Containing Nucleosomes in the Male Pronucleus
Orsi GA, Algazeery A, Meyer RE, Capri M, Sapey-Triomphe LM, Horard B, Gruffat H, Couble P, Aït-Ahmed O, Loppin B.
Dissecting the Structure and Mechanism of a Complex Duplication-Triplication Rearrangement in the DMD Gene
Ishmukhametova A, Chen JM, Bernard R, de Massy B, Baudat F, Boyer A, Méchin D, Thorel D, Chabrol B, Vincent MC, Van Kien PK, Claustres M, Tuffery-Giraud S.
SPO11-Independent DNA Repair Foci and Their Role in Meiotic Silencing
Carofiglio F, Inagaki A, de Vries S, Wassenaar E, Schoenmakers S, Vermeulen C, van Cappellen WA, Sleddens-Linkels E, Grootegoed JA, Te Riele HP, de Massy B, Baarends WM.
Cellular Source and Mechanisms of High Transcriptome Complexity in the Mammalian Testis
Soumillon M, Necsulea A, Weier M, Brawand D, Zhang X, Gu H, Barthès P, Kokkinaki M, Nef S, Gnirke A, Dym M, de Massy B, Mikkelsen TS, Kaessmann H.
Initation of Meiotic Recombination: How and Where? Conversation and Specificities Among Eukaryotes.
De massy, B.
Molecular Basis for the Regulation of the H3K4 Methyltransferase Activity of PRDM9.
Wu H, Mathioudakis N, Diagouraga B, Dong A, Dombrovski L, Baudat F, Cusack S, de Massy B, Kadlec J.
Meiotic recombination in mammals: localization and regulation
Baudat F, Imai Y, de Massy B.
Interallelic and intergenic incompatibilities of the prdm9 (hst1) gene in mouse hybrid sterility
Flachs P, Mihola O, Simeček P, Gregorová S, Schimenti JC, Matsui Y, Baudat F, de Massy B, Piálek J, Forejt J, Trachtulec Z.
The Glucocorticoid-Induced Leucine Zipper (GILZ) Is Essential for Spermatogonial Survival and Spermatogenesis
Romero Y, Vuandaba M, Suarez P, Grey C, Calvel P, Conne B, Pearce D, de Massy B, Hummler E, Nef S.
The Molecular Chaperone Hsp90α Is Required for Meiotic Progression of Spermatocytes beyond Pachytene in the Mouse
Grad I, Cederroth CR, Walicki J, Grey C, Barluenga S, Winssinger N, De Massy B, Nef S, Picard D
What defines the genetic map? The specification of meiotic recombination sites.
Grey C, Sommermeyer V, Borde V, de Massy B
The Impressionistic Landscape of Meiotic Recombination
Lichten, M., de Massy, B.
Dicer1 depletion in male germ cells leads to infertility due to cumulative meiotic and spermiogenic defects.
Romero Y, Meikar O, Papaioannou MD, Conne B, Grey C, Weier M, Pralong F, De Massy B, Kaessmann H, Vassalli JD, Kotaja N, Nef S.
Mouse PRDM9 DNA-Binding Specificity Determines Sites of Histone H3 Lysine 4 Trimethylation for Initiation of Meiotic Recombination.
Grey C, Barthès P, Chauveau-Le Friec G, Langa F, Baudat F, de Massy B.
What determines the localisation of spots of meiotic recombination?
Baudat F, Buard J, Grey C, de Massy B.
PRDM9 Is a Major Determinant of Meiotic Recombination Hotspots in Humans and Mice
Baudat, F., Buard, J., Grey, C., Fledel-Alon, A., Ober, C., Przeworski, M., Coop, G., de Massy, B.
Functional conservation of Mei4 for meiotic DNA double-strand break formation from yeasts to mice
Kumar, R., Bourbon, H.M., De Massy, B.
Prdm9, a key control of mammalian recombination hotspots
Baudat F, Buard J, Grey C, de Massy B.
A single mutation results in diploid gamete formation and parthenogenesis in a Drosophila yemanuclein-alpha meiosis I defective mutant
Meyer, RE., Delaage, M., Rosset, R., Capri, M., Ait-Ahmed, O.
Parallel detection of crossovers and non-crossovers in mouse germ cells.
Baudat, F. and de Massy, B.
Genome-Wide Control of the Distribution of Meiotic Recombination.
Grey C, Baudat F, de Massy B.
Mutation of the mouse Syce1 gene disrupts synapsis and suggests a link between synaptonemal complex structural components and DNA repair.
Bolcun-Filas, E., Speed, R., Taggart, M., Grey, C., de Massy, B., Benavente, R., Cooke, HJ.
Distinct histone modifications define initiation and repair of meiotic recombination in mouse
Buard, J., Barthès, P., Grey, C. and de Massy, B_.
Repeat Length and RNA Expression Level Are Not Primary Determinants in CUG Expansion Toxicity in Drosophila Models
Le Mée, G., Ezzeddine, N., Capri, M., Aït-Ahmed, O.
Distinct Functions of MLH3 at Recombination Hot Spots in the Mouse.
Svetlanov A, Baudat F, Cohen PE, de Massy B.
Playing hide and seek with mammalian meiotic crossover hotspots.
Buard, J., De Massy, B.
Characterization of Spo11-dependent and independent phospho-H2AX foci during meiotic prophase I in the male mouse
Chicheportiche A, Bernardino-Sgherri J, de Massy B, Dutrillaux B.
Cis- and Trans-Acting Elements Regulate the Mouse Psmb9 Meiotic Recombination Hotspot.
Baudat, F., de Massy, B
Regulating double-stranded DNA break repair towards crossover or non-crossover during mammalian meiosis
Baudat, F., de Massy, B.
Oligomerization of EDEN-BP is required for specific mRNA deadenylation and binding.
Cosson, B., Gautier-Courteille, C., Maniey, D., Ait-Ahmed, O., Lesimple, M., Osborne, H.B., Paillard, L.
A Fast and Specific Alignment Method for Minisatellite Maps
Bérard S., Buard J. et E. Rivals.
Crossover and noncrossover pathways in mouse meiosis.
Guillon, H., Baudat, F., Grey, C., Liskay, R.M. and de Massy, B
Manipulating multiple sequence alignments via MaM and WebMaM
Alkan, C., Tuzun, E., Buard, J., Lethiec, F., Eichler, EE., Bailey JA., Sahinalp, SC.
Male cell microchimerism in normal and diseased female livers from fetal life to adulthood
Guettier, C., Sebagh, M., Buard, J., Feneux, D., Ortin-Serrano, M., Gigou, M., Tricottet, V., Reynes, M., Samuel, D., Feray, C.
The Drosophila Bruno paralogue Bru-3 specifically binds the EDEN translational repression element.
Delaunay J, Le Mée G, Ezzeddine N, Labesse G, Terzian C, Capri M, Aït-Ahmed O.
Recombination across the centromere of disjoined and non-disjoined chromosomes 21
Laurent, A. M., Li, M., Sherman, S., Roizes, G., Buard, J.,
Distribution of meiotic recombination sites
de Massy, B.
EDEN-dependent translational repression of maternal mRNAs is conserved between Xenopus and Drosophila
Ezzeddine, N., Paillard, L., Capri, M., Maniey, D., Bassez, T., Aït-Ahmed, O. and Osborne, H.B.
Instability of the human minisatellite CEB1 in rad27Delta and dna2-1 replication-deficient yeast cells.
Lopes J., Debrauwere H., Buard J., Nicolas A.
Evolutionary fate of an unstable human minisatellite deduced from sperm-mutation spectra of individual alleles.
Buard J., Brenner C., Jeffreys A.J.
An initiation site for meiotic crossing-over and gene conversion in the mouse
Guillon H. and de Massy B.
Identification and characterization of an Spo11 homolog in the mouse
Metzler-Guillemain, C. et de Massy B.
Somatic versus germline mutation processes at minisatellite CEB1 (D2S90) in humans and transgenic mice
Buard J., Collick A., Brown J. and Jeffreys, A.J.
Meiotic recombination and flanking marker exchange at the highly unstable human minisatellite CEB1 (D2S90)
Buard, J., Shone, A.C. and Jeffreys, A.J.
Mécanisme d’instabilité des minisatellites.
Debrauwere H., Nicolas A., Vergnaud G., Buard J., Tessier J. et Aubert D.
Influence of allele lineage on the role of the insulin minisatellite in susceptibility to type 1 diabetes.
Stead JD, Buard J, Todd JA, Jeffreys AJ.
The essential role of yeast topoisomerase III in meiosis depends on recombination.
Gangloff, S., De Massy, B., Lane, A., Rothstein, R. and Fabre, F.
Meiotic instability of human minisatellite CEB1 in yeast requires DNA double-strand breaks.
Debrauwere H, Buard J, Tessier J, Aubert D, Vergnaud G, Nicolas A.
Implication of a 5'coding sequence in targeting maternal mRNA to the Drosophila oocyte.
Capri, M., Santoni, M.J., Thomas-Delaage, M. and Aït-Ahmed, O.
Mitotic recombination and localized DNA double-strand breaks are induced after 8-methoxy psoralen and UVA irradiation in Saccharomyces cerevisia.
Dardhalon, M., De Massy, B., Nicolas, A. and Averbeck, D.
A sequence based computational identification of Drosophila developmentally regulated TATA-less NA polymerase II promoter and its experimental validation.
Santoni, M.J., Aït-Ahmed, O. and Marilley, M.
PUBLICATIONS COMMUNES
A Testis-Specific Chaperone and the Chromatin Remodeler ISWI Mediate Repackaging of the Paternal Genome
Doyen CM1, Chalkley GE1, Voets O1, Bezstarosti K2, Demmers JA2, Moshkin YM1, Verrijzer CP3.
2015 - Cell Rep
, 13, 7, 1310-1318 26549447 
Service porteur :
Virologie Moléculaire
Anatomical and Molecular Analyses of XY Ovaries from the African Pygmy Mouse Mus minutoides
Rahmoun M, Perez J, Saunders PA, Boizet-Bonhoure B, Wilhelm D, Poulat F, Veyrunes F.
2014 - Sex Dev.
, 8, 6, 356-363 25359508
Service porteur :
Développement et Pathologie de la Gonade
Maraviroc-induced decrease in circulating bacterial products is not linked to an increase in immune activation in HIV-infected individuals.
Psomas C, Lavigne JP, Barbuat C, Trabelsi S, Ghosn J, Lascoux-Combe C, Flandre P, Cuzin L, Reynes J, Autran B, Corbeau P.
2013 - Blood
, 122(13):2282-3.
Service porteur :
Domiciliation, activation immunitaire et infection
MCM8- and MCM9-Deficient Mice Reveal Gametogenesis Defects and Genome Instability Due to Impaired Homologous Recombination
Lutzmann M, Grey C, Traver S, Ganier O, Maya-Mendoza A, Ranisavljevic N, Bernex F, Nishiyama A, Montel N, Gavois E, Forichon L, de Massy B, Méchali M.
2012 - Mol. Cell
, 47, 4, 523-534 22771120
Service porteur :
Réplication et Dynamique du Génome
The regulation of competence to replicate in meiosis by Cdc6 is conserved during evolution.
Lemaitre, JM., Bocquet, S., Terret, ME., Namdar, M., Ait-Ahmed, O., Kearsey, S., Verlhac, MH., and Méchali, M.
2004 - Mol Reprod Dev.
, 69, 94-100 15278909
Service porteur :
Réplication et Dynamique du Génome
Responsable : Bernard DE MASSY
contacter le service
financeurs
