CCP1/Nna1 functions in protein turnover in mouse brain: Implications for cell death in Purkinje cell degeneration mice


Autoria(s): BEREZNIUK, Iryna; SIRONI, Juan; CALLAWAY, Myrasol B.; CASTRO, Leandro M.; HIRATA, Izaura Y.; FERRO, Emer S.; FRICKER, Lloyd D.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

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

http://dx.doi.org/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