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1.
Glia ; 60(4): 515-25, 2012 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-22105777

RESUMO

Emerging evidence suggests that p53, a tumor suppressor protein primarily involved in cancer biology, coordinates a wide range of novel functions in the CNS including the mediation of pathways underlying neurodegenerative disease pathogenesis. Moreover, an evolving concept in cell and molecular neuroscience is that glial cells are far more fundamental to disease progression than previously thought, which may occur via a noncell-autonomous mechanism that is heavily dependent on p53 activities. As a crucial hub connecting many intracellular control pathways, including cell-cycle control and apoptosis, p53 is ideally placed to coordinate the cellular response to a range of stresses. Although neurodegenerative diseases each display a distinct and diverse molecular pathology, apoptosis is a widespread hallmark feature and the multimodal capacity of the p53 system to orchestrate apoptosis and glial cell behavior highlights p53 as a potential unifying target for therapeutic intervention in neurodegeneration.


Assuntos
Doenças do Sistema Nervoso/patologia , Neuroglia/metabolismo , Proteína Supressora de Tumor p53/metabolismo , Animais , Humanos , Neurônios/metabolismo , Transdução de Sinais
2.
Sci Rep ; 2: 695, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23019516

RESUMO

The ROCO proteins are a family of large, multidomain proteins characterised by the presence of a Ras of complex proteins (ROC) domain followed by a COR, or C-terminal of ROC, domain. It has previously been shown that the ROC domain of the human ROCO protein Leucine Rich Repeat Kinase 2 (LRRK2) controls its kinase activity. Here, the ability of the ROC domain of another human ROCO protein, Death Associated Protein Kinase 1 (DAPK1), to bind GTP and control its kinase activity has been evaluated. In contrast to LRRK2, loss of GTP binding by DAPK1 does not result in loss of kinase activity, instead acting to modulate this activity. These data highlight the ROC domain of DAPK1 as a target for modifiers of this proteins function, and casts light on the role of ROC domains as intramolecular regulators in complex proteins with implications for a broad range of human diseases.


Assuntos
Proteínas Reguladoras de Apoptose/química , Proteínas Reguladoras de Apoptose/metabolismo , Proteínas Quinases Dependentes de Cálcio-Calmodulina/química , Proteínas Quinases Dependentes de Cálcio-Calmodulina/metabolismo , Guanosina Trifosfato/metabolismo , Domínios e Motivos de Interação entre Proteínas , Animais , Proteínas Reguladoras de Apoptose/genética , Proteínas de Bactérias/química , Proteínas de Bactérias/metabolismo , Proteínas Quinases Dependentes de Cálcio-Calmodulina/genética , Linhagem Celular , Chlorobium/química , Proteínas Quinases Associadas com Morte Celular , Guanosina Trifosfato/química , Células HEK293 , Humanos , Simulação de Acoplamento Molecular , Mutação , Ligação Proteica , Conformação Proteica , Transporte Proteico
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