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1.
J Biol Chem ; 288(34): 24452-64, 2013 Aug 23.
Artigo em Inglês | MEDLINE | ID: mdl-23861403

RESUMO

In acute and chronic neurodegeneration, Ca(2+) mishandling and disruption of the cytoskeleton compromise neuronal integrity, yet abnormalities in the signaling roles of cytoskeletal proteins remain largely unexplored. We now report that the microtubule-associated protein p600 (also known as UBR4) promotes neuronal survival. Following depletion of p600, glutamate-induced Ca(2+) influx through NMDA receptors, but not AMPA receptors, initiates a degenerative process characterized by endoplasmic reticulum fragmentation and endoplasmic reticulum Ca(2+) release via inositol 1,4,5-trisphosphate receptors. Downstream of NMDA receptors, p600 associates with the calmodulin·calmodulin-dependent protein kinase IIα complex. A direct and atypical p600/calmodulin interaction is required for neuronal survival. Thus, p600 counteracts specific Ca(2+)-induced death pathways through regulation of Ca(2+) homeostasis and signaling.


Assuntos
Cálcio/metabolismo , Proteínas de Ligação a Calmodulina/metabolismo , Proteínas Associadas aos Microtúbulos/metabolismo , Proteínas do Tecido Nervoso/metabolismo , Neurônios/metabolismo , Transdução de Sinais/fisiologia , Animais , Proteínas de Ligação a Calmodulina/genética , Sobrevivência Celular/fisiologia , Células Cultivadas , Ácido Glutâmico/genética , Ácido Glutâmico/metabolismo , Proteínas Associadas aos Microtúbulos/genética , Proteínas do Tecido Nervoso/genética , Neurônios/citologia , Ratos , Receptores de AMPA/genética , Receptores de AMPA/metabolismo , Receptores de N-Metil-D-Aspartato/genética , Receptores de N-Metil-D-Aspartato/metabolismo
2.
J Biol Chem ; 286(27): 23831-41, 2011 Jul 08.
Artigo em Inglês | MEDLINE | ID: mdl-21555516

RESUMO

Initiation of eukaryotic genome duplication begins when a six-subunit origin recognition complex (ORC) binds to DNA. However, the mechanism by which this occurs in vivo and the roles played by individual subunits appear to differ significantly among organisms. Previous studies identified a soluble human ORC(2-5) complex in the nucleus, an ORC(1-5) complex bound to chromatin, and an Orc6 protein that binds weakly, if at all, to other ORC subunits. Here we show that stable ORC(1-6) complexes also can be purified from human cell extracts and that Orc6 and Orc1 each contain a single nuclear localization signal that is essential for nuclear localization but not for ORC assembly. The Orc6 nuclear localization signal, which is essential for Orc6 function, is facilitated by phosphorylation at its cyclin-dependent kinase consensus site and by association with Kpna6/1, nuclear transport proteins that did not co-purify with other ORC subunits. These and other results support a model in which Orc6, Orc1, and ORC(2-5) are transported independently to the nucleus where they can either assemble into ORC(1-6) or function individually.


Assuntos
Núcleo Celular/metabolismo , Modelos Biológicos , Complexo de Reconhecimento de Origem/metabolismo , alfa Carioferinas/metabolismo , Transporte Ativo do Núcleo Celular/fisiologia , Núcleo Celular/genética , Células HeLa , Humanos , Complexo de Reconhecimento de Origem/genética , Fosforilação/fisiologia , alfa Carioferinas/genética
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