Genomic stability and tumour suppression by the APC/C cofactor Cdh1.

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...

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Detalhes bibliográficos
Autores: García-Higuera, Irene, Manchado, Eusebio, Dubus, Pierre, Cañamero, Marta, Mendez, Juan, Moreno, Sergio, Malumbres, Marcos
Tipo de documento: artigo
Data de publicação:2008
País:España
Recursos:Instituto de Salud Carlos III (ISCIII)
Repositório:Repisalud
Idioma:inglês
OAI Identifier:oai:repisalud.isciii.es:20.500.12105/17955
Acesso em linha:http://hdl.handle.net/20.500.12105/17955
Access Level:Acceso aberto
Palavra-chave:Genomic Instability
Anaphase-Promoting Complex-Cyclosome
Animals
Behavior, Animal
Brain
Cdh1 Proteins
Cell Cycle
Cell Cycle Proteins
Cell Proliferation
Cells, Cultured
Chromosome Aberrations
Embryo, Mammalian
Female
Fibroblasts
Mice
Mice, Knockout
Mice, Transgenic
Neoplasms
Placenta
Pregnancy
Tumor Suppressor Proteins
Ubiquitin-Protein Ligase Complexes
Descrição
Resumo: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.