Publication: Genomic stability and tumour suppression by the APC/C cofactor Cdh1.
| dc.contributor.author | García-Higuera, Irene | |
| dc.contributor.author | Manchado, Eusebio | |
| dc.contributor.author | Dubus, Pierre | |
| dc.contributor.author | Cañamero, Marta | |
| dc.contributor.author | Mendez, Juan | |
| dc.contributor.author | Moreno, Sergio | |
| dc.contributor.author | Malumbres, Marcos | |
| dc.contributor.funder | Ministerio de Educación y Ciencia (España) | |
| dc.contributor.funder | Comunidad de Madrid (España) | |
| dc.contributor.funder | Fundación Ramón Areces | |
| dc.contributor.funder | Fundación Médica Mutua Madrileña Automovilística | es_ES |
| dc.contributor.funder | Asociación Española Contra el Cáncer | |
| dc.date.accessioned | 2024-02-12T10:34:15Z | |
| dc.date.available | 2024-02-12T10:34:15Z | |
| dc.date.issued | 2008-07 | |
| dc.description.abstract | The anaphase promoting complex or cyclosome (APC/C) is a ubiquitin protein ligase that, together with Cdc20 or Cdh1, targets cell-cycle proteins for degradation. APC/C-Cdh1 specifically promotes protein degradation in late mitosis and G1. Mutant embryos lacking Cdh1 die at E9.5-E10.5 due to defects in the endoreduplication of trophoblast cells and placental malfunction. This lethality is prevented when Cdh1 is expressed in the placenta. Cdh1-deficient cells proliferate inefficiently and accumulate numeric and structural chromosomal aberrations, indicating that Cdh1 contributes to the maintenance of genomic stability. Cdh1 heterozygous animals show increased susceptibility to spontaneous tumours, suggesting that Cdh1 functions as a haploinsufficient tumour suppressor. These heterozygous mice also show several defects in behaviour associated with increased proliferation of stem cells in the nervous system. These results indicate that Cdh1 is required for preventing unscheduled proliferation of specific progenitor cells and protecting mammalian cells from genomic instability. | es_ES |
| dc.description.peerreviewed | Sí | es_ES |
| dc.description.sponsorship | This work was supported by grants from the Association pour la Recherche contre le Cancer and the Région Aquitaine (to P.D.), Ministerio de Educación y Ciencia (SAF2004- 05611 to I.G.H.; BFU2004-04886 to J.M.; BFU2005-03195 and GEN2003-20243-C08-05 to S.M.; and SAF2006-05186 to M.M.), the Consolider-Ingenio 2010 Programme (CSD2007- 00015 to J.M. and S.M.; and CSD2007-00017 to M.M.), Comunidad de Madrid (OncoCycle Programme; S-BIO-0283-2006), Fundación Ramón Areces, and Fundación Médica Mutua Madrileña Automovilística (to M.M.); and Fundación Científica de la Asociación Española contra el Cáncer (to S.M. and M.M.). | es_ES |
| dc.format.number | 7 | es_ES |
| dc.format.page | 802 | es_ES |
| dc.format.volume | 10 | es_ES |
| dc.identifier.citation | Nat Cell Biol . 2008;10(7):802-11. | es_ES |
| dc.identifier.doi | 10.1038/ncb1742 | es_ES |
| dc.identifier.e-issn | 1476-4679 | es_ES |
| dc.identifier.journal | Nature cell biology | es_ES |
| dc.identifier.pubmedID | 18552834 | es_ES |
| dc.identifier.uri | http://hdl.handle.net/20.500.12105/17955 | |
| dc.language.iso | eng | es_ES |
| dc.publisher | Nature Publishing Group | |
| dc.relation.projectFIS | info:eu-repo/grantAgreement/ES/SAF2004- 05611 | es_ES |
| dc.relation.projectFIS | info:eu-repo/grantAgreement/ES/BFU2004-04886 | es_ES |
| dc.relation.projectFIS | info:eu-repo/grantAgreement/ES/BFU2005-03195 | es_ES |
| dc.relation.projectFIS | info:eu-repo/grantAgreement/ES/GEN2003-20243-C08-05 | es_ES |
| dc.relation.projectFIS | info:eu-repo/grantAgreement/ES/SAF2006-05186 | es_ES |
| dc.relation.projectFIS | info:eu-repo/grantAgreement/ES/CSD2007- 00015 | es_ES |
| dc.relation.projectFIS | info:eu-repo/grantAgreement/ES/CSD2007-00017 | es_ES |
| dc.relation.publisherversion | https://doi.org/10.1038/ncb1742 | es_ES |
| dc.repisalud.institucion | CNIO | es_ES |
| dc.repisalud.orgCNIO | CNIO::Grupos de investigación::Grupo de Replicación de ADN | es_ES |
| dc.rights.accessRights | open access | es_ES |
| dc.rights.license | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
| dc.subject.mesh | Genomic Instability | es_ES |
| dc.subject.mesh | Anaphase-Promoting Complex-Cyclosome | es_ES |
| dc.subject.mesh | Animals | es_ES |
| dc.subject.mesh | Behavior, Animal | es_ES |
| dc.subject.mesh | Brain | es_ES |
| dc.subject.mesh | Cdh1 Proteins | es_ES |
| dc.subject.mesh | Cell Cycle | es_ES |
| dc.subject.mesh | Cell Cycle Proteins | es_ES |
| dc.subject.mesh | Cell Proliferation | es_ES |
| dc.subject.mesh | Cells, Cultured | es_ES |
| dc.subject.mesh | Chromosome Aberrations | es_ES |
| dc.subject.mesh | Embryo, Mammalian | es_ES |
| dc.subject.mesh | Female | es_ES |
| dc.subject.mesh | Fibroblasts | es_ES |
| dc.subject.mesh | Mice | es_ES |
| dc.subject.mesh | Mice, Knockout | es_ES |
| dc.subject.mesh | Mice, Transgenic | es_ES |
| dc.subject.mesh | Neoplasms | es_ES |
| dc.subject.mesh | Placenta | es_ES |
| dc.subject.mesh | Pregnancy | es_ES |
| dc.subject.mesh | Tumor Suppressor Proteins | es_ES |
| dc.subject.mesh | Ubiquitin-Protein Ligase Complexes | es_ES |
| dc.title | Genomic stability and tumour suppression by the APC/C cofactor Cdh1. | es_ES |
| dc.type | journal article | es_ES |
| dc.type.hasVersion | AO | es_ES |
| dspace.entity.type | Publication | |
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