Cargando…

C14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertility

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 in...

Descripción completa

Detalles Bibliográficos
Autores principales: Gómez-H, Laura, Felipe-Medina, Natalia, Sánchez-Martín, Manuel, Davies, Owen R., Ramos, Isabel, García-Tuñón, Ignacio, de Rooij, Dirk G., Dereli, Ihsan, Tóth, Attila, Barbero, José Luis, Benavente, Ricardo, Llano, Elena, Pendas, Alberto M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095591/
https://www.ncbi.nlm.nih.gov/pubmed/27796301
http://dx.doi.org/10.1038/ncomms13298
_version_ 1782465309710483456
author Gómez-H, Laura
Felipe-Medina, Natalia
Sánchez-Martín, Manuel
Davies, Owen R.
Ramos, Isabel
García-Tuñón, Ignacio
de Rooij, Dirk G.
Dereli, Ihsan
Tóth, Attila
Barbero, José Luis
Benavente, Ricardo
Llano, Elena
Pendas, Alberto M.
author_facet Gómez-H, Laura
Felipe-Medina, Natalia
Sánchez-Martín, Manuel
Davies, Owen R.
Ramos, Isabel
García-Tuñón, Ignacio
de Rooij, Dirk G.
Dereli, Ihsan
Tóth, Attila
Barbero, José Luis
Benavente, Ricardo
Llano, Elena
Pendas, Alberto M.
author_sort Gómez-H, Laura
collection PubMed
description 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.
format Online
Article
Text
id pubmed-5095591
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-50955912016-11-18 C14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertility Gómez-H, Laura Felipe-Medina, Natalia Sánchez-Martín, Manuel Davies, Owen R. Ramos, Isabel García-Tuñón, Ignacio de Rooij, Dirk G. Dereli, Ihsan Tóth, Attila Barbero, José Luis Benavente, Ricardo Llano, Elena Pendas, Alberto M. Nat Commun Article 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. Nature Publishing Group 2016-10-31 /pmc/articles/PMC5095591/ /pubmed/27796301 http://dx.doi.org/10.1038/ncomms13298 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Gómez-H, Laura
Felipe-Medina, Natalia
Sánchez-Martín, Manuel
Davies, Owen R.
Ramos, Isabel
García-Tuñón, Ignacio
de Rooij, Dirk G.
Dereli, Ihsan
Tóth, Attila
Barbero, José Luis
Benavente, Ricardo
Llano, Elena
Pendas, Alberto M.
C14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertility
title C14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertility
title_full C14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertility
title_fullStr C14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertility
title_full_unstemmed C14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertility
title_short C14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertility
title_sort c14orf39/six6os1 is a constituent of the synaptonemal complex and is essential for mouse fertility
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095591/
https://www.ncbi.nlm.nih.gov/pubmed/27796301
http://dx.doi.org/10.1038/ncomms13298
work_keys_str_mv AT gomezhlaura c14orf39six6os1isaconstituentofthesynaptonemalcomplexandisessentialformousefertility
AT felipemedinanatalia c14orf39six6os1isaconstituentofthesynaptonemalcomplexandisessentialformousefertility
AT sanchezmartinmanuel c14orf39six6os1isaconstituentofthesynaptonemalcomplexandisessentialformousefertility
AT daviesowenr c14orf39six6os1isaconstituentofthesynaptonemalcomplexandisessentialformousefertility
AT ramosisabel c14orf39six6os1isaconstituentofthesynaptonemalcomplexandisessentialformousefertility
AT garciatunonignacio c14orf39six6os1isaconstituentofthesynaptonemalcomplexandisessentialformousefertility
AT derooijdirkg c14orf39six6os1isaconstituentofthesynaptonemalcomplexandisessentialformousefertility
AT dereliihsan c14orf39six6os1isaconstituentofthesynaptonemalcomplexandisessentialformousefertility
AT tothattila c14orf39six6os1isaconstituentofthesynaptonemalcomplexandisessentialformousefertility
AT barberojoseluis c14orf39six6os1isaconstituentofthesynaptonemalcomplexandisessentialformousefertility
AT benaventericardo c14orf39six6os1isaconstituentofthesynaptonemalcomplexandisessentialformousefertility
AT llanoelena c14orf39six6os1isaconstituentofthesynaptonemalcomplexandisessentialformousefertility
AT pendasalbertom c14orf39six6os1isaconstituentofthesynaptonemalcomplexandisessentialformousefertility