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J Cell Sci ; 133(4)2020 02 21.
Artigo em Inglês | MEDLINE | ID: mdl-31974111

RESUMO

The centrosome linker serves to hold the duplicated centrosomes together until they separate in late G2/early mitosis. Precisely how the linker is assembled remains an open question. In this study, we identify Cep44 as a novel component of the linker in human cells. Cep44 localizes to the proximal end of centrioles, including mother and daughter centrioles, and its ablation leads to loss of centrosome cohesion. Cep44 does not impinge on the stability of C-Nap1 (also known as CEP250), LRRC45 or Cep215 (also known as CDK5RAP2), and vice versa, and these proteins are independently recruited to the centrosome. Rather, Cep44 associates with rootletin and regulates its stability and localization to the centrosome. Our findings reveal a role of the previously uncharacterized protein Cep44 for centrosome cohesion and linker assembly.


Assuntos
Centrossomo , Proteínas do Citoesqueleto , Autoantígenos , Proteínas de Ciclo Celular/genética , Centríolos , Proteínas do Citoesqueleto/genética , Humanos , Mitose , Proteínas do Tecido Nervoso
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