DJ-1 cooperates with PYCR1 in cell protection against oxidative stress

被引:45
|
作者
Yasuda, Tatsuki [1 ,2 ]
Kaji, Yusuke [1 ,2 ]
Agatsuma, Tomohiro [1 ,2 ]
Niki, Takeshi [2 ]
Arisawa, Mitsuhiro [3 ]
Shuto, Satoshi [3 ]
Ariga, Hiroyoshi [3 ]
Iguchi-Ariga, Sanae M. M. [2 ]
机构
[1] Hokkaido Univ, Grad Sch Life Sci, Sapporo, Hokkaido 0608589, Japan
[2] Hokkaido Univ, Fac Agr, Sapporo, Hokkaido 0608589, Japan
[3] Hokkaido Univ, Fac Pharmaceut Sci, Sapporo, Hokkaido 0600812, Japan
关键词
DJ-1; PYCR1; Proline; Oxidative stress; Apoptosis; TRANSFORMATION; MUTATIONS; ONCOGENE; GENE;
D O I
10.1016/j.bbrc.2013.05.095
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DJ-1, a product of the DJ-1/PARK7 gene, has been suggested to play various functions involved in transcriptional regulation, protease activity, anti-oxidative stress. activity, and regulation of mitochondrial complex I. Such a variety of functions of DJ-1 are supposed to be realized through interactions with different partner proteins. Among the candidates for DJ-1-partner proteins detected in TOF-MAS analyses of the cellular proteins co-immunoprecipitated with DJ-1, we focused here pyrroline-5-carboxylate reductase 1, PYCR1, a final key enzyme for proline biosynthesis. DJ-1 directly bound to PYCR1 in vivo and in vitro. DJ-1 and PYCR1 colocalized in mitochondria, and both were suggested to be involved in regulation of mitochondrial membrane potential, but differently. DJ-1 enhanced the enzymatic activity of PYCR1 in vitro. The cells knocked down for DJ-1 and PYCR1 showed lower viability under oxidative stress conditions. No additive nor synergistic results were obtained for the cells that had been knocked down for both DJ-1 and PYCR1, suggesting that DJ-1 and PYCR1 are on the same pathway of anti-oxidative stress protection of the cells. (C) 2013 Elsevier Inc. All rights reserved.
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页码:289 / 294
页数:6
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