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dc.contributor.authorGómez Hernández, Laura
dc.contributor.authorFelipe-Medina, Natalia
dc.contributor.authorSánchez Martín, Manuel Adolfo 
dc.contributor.authorDavies, Owen R.
dc.contributor.authorRamos, Isabel
dc.contributor.authorGarcía-Tuñón, Ignacio
dc.contributor.authorde Rooij, Dirk G.
dc.contributor.authorDereli, Ihsan
dc.contributor.authorTóth, Attila
dc.contributor.authorBarbero, José Luis
dc.contributor.authorBenavente, Ricardo
dc.contributor.authorLlano Cuadra, María Elena 
dc.contributor.authorPendás, Alberto M. 
dc.date.accessioned2020-09-01T10:59:05Z
dc.date.available2020-09-01T10:59:05Z
dc.date.issued2016
dc.identifier.citationGómez-H, L., Felipe-Medina, N., Sánchez-Martín, M. et al. C14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertility. Nat Commun 7, 13298 (2016). https://doi.org/10.1038/ncomms13298es_ES
dc.identifier.urihttp://hdl.handle.net/10366/143908
dc.description.abstract[EN]Meiotic recombination generates crossovers between homologous chromosomes that are essential for genome haploidization. The synaptonemal complex is a ‘zipper’-like protein assembly that synapses homologue pairs together and provides the structural framework for processing recombination sites into crossovers. Humans show individual differences in the number of crossovers generated across the genome. Recently, an anonymous gene variant in C14ORF39/SIX6OS1 was identified that influences the recombination rate in humans. Here we show that C14ORF39/SIX6OS1 encodes a component of the central element of the synaptonemal complex. Yeast two-hybrid analysis reveals that SIX6OS1 interacts with the well-established protein synaptonemal complex central element 1 (SYCE1). Mice lacking SIX6OS1 are defective in chromosome synapsis at meiotic prophase I, which provokes an arrest at the pachytene-like stage and results in infertility. In accordance with its role as a modifier of the human recombination rate, SIX6OS1 is essential for the appropriate processing of intermediate recombination nodules before crossover formation.es_ES
dc.description.sponsorshipThis work was supported by BFU_2014-59307-R, MEIONet and JCyLe (CSI052U16). LGH and NFM are supported by European Social Fund/JCyLe grants (EDU/1083/2013 and EDU/310/2015). ORD is a Sir Henry Dale Fellow jointly funded by the Wellcome Trust and Royal Society (Grant Number 104158/Z/14/Z). RB is funded by DFG (grant Be1168/8-1). AT and ID were supported by DFG grants TO421/8-2 and TO421/6-1, respectively.es_ES
dc.format.mimetypeapplication/pdf
dc.language.isoenges_ES
dc.publisherNature Publishing Group (Londres, Gran Bretaña)es_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectChromosomeses_ES
dc.subjectMeiosises_ES
dc.subjectSpermatogenesises_ES
dc.subject.meshSpermatogenesis*
dc.subject.meshMeiosis*
dc.subject.meshChromosomes*
dc.titleC14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertilityes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1038/ncomms13298
dc.subject.unesco2415 Biología Moleculares_ES
dc.identifier.doi10.1038/ncomms13298es_ES
dc.relation.projectIDMINECO/ICTI2013-2016/BFU2014-59307-Res_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn2041-1723
dc.journal.titleNature Communicationses_ES
dc.volume.number7es_ES
dc.issue.number1es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsmeiosis*
dc.subject.decscromosomas*
dc.subject.decsespermatogénesis*


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internacional