CCP1/Nna1 functions in protein turnover in mouse brain: Implications for cell death in Purkinje cell degeneration mice
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2010
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Resumo |
Purkinje cell degeneration (pcd) mice have a mutation within the gene encoding cytosolic carboxypeptidase 1 (CCP1/Nna1), which has homology to metallocarboxypeptidases. To assess the function of CCP1/Nna1, quantitative proteomics and peptidomics approaches were used to compare proteins and peptides in mutant and wild-type mice. Hundreds of peptides derived from cytosolic and mitochondrial proteins are greatly elevated in pcd mouse hypothalamus, amygdala, cortex, prefrontal cortex, and striatum. However, the major proteins detected on 2-D gel electrophoresis were present in mutant and wild-type mouse cortex and hypothalamus at comparable levels, and proteasome activity is normal in these brain regions of pcd mice, suggesting that the increase in cellular peptide levels in the pcd mice is due to reduced degradation of the peptides downstream of the proteasome. Both nondegenerating and degenerating regions of pcd mouse brain, but not wild-type mouse brain, show elevated autophagy, which can be triggered by a decrease in amino acid levels. Taken together with previous studies on CCP1/Nna1, these data suggest that CCP1/Nna1 plays a role in protein turnover by cleaving proteasome-generated peptides into amino acids and that decreased peptide turnover in the pcd mice leads to cell death.-Berezniuk, I., Sironi, J., Callaway, M. B., Castro, L. M., Hirata, I. Y., Ferro, E. S., Fricker, L. D. CCP1/Nna1 functions in protein turnover in mouse brain: Implications for cell death in Purkinje cell degeneration mice. FASEB J. 24, 1813-1823 (2010). www.fasebj.org U.S. National Institutes of Health (NIH) National Institutes of Health (NIH)[DK-51271] National Institutes of Health (NIH)[DA-04494] U.S. National Institutes of Health (NIH) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[04/04933-2] FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[04/14846-0] Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Financiadora de Estudos e Projetos (FINEP)[A-03/134] Financiadora de Estudos e Projetos (FINEP) CNPq Conselho Nacional de Desenvolvimento Cientifico e Tecnologico Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Universidade de Campinas (UNICAMP), Campinas, SP, Brazil Universidade Estadual de Campinas (UNICAMP) |
Identificador |
FASEB JOURNAL, v.24, n.6, p.1813-1823, 2010 0892-6638 http://producao.usp.br/handle/BDPI/28079 10.1096/fj.09-147942 |
Idioma(s) |
eng |
Publicador |
FEDERATION AMER SOC EXP BIOL |
Relação |
Faseb Journal |
Direitos |
restrictedAccess Copyright FEDERATION AMER SOC EXP BIOL |
Palavras-Chave | #proteasome #carboxypeptidase #aminopeptidase #protein degradation #neurodegeneration #CEREBELLAR MUTANT MOUSE #PCD MUTANT #THIMET OLIGOPEPTIDASE #RETINAL DEGENERATION #MASS-SPECTROMETRY #WILD-TYPE #PEPTIDES #NNA1 #NEUROPEPTIDOMICS #DEGRADATION #Biochemistry & Molecular Biology #Biology #Cell Biology |
Tipo |
article original article publishedVersion |