Multiple oxidative stress-response members of the Adapt78 family

被引:19
作者
Michtalik, HJ
Narayan, AV
Bhatt, N
Lin, HY
Mulligan, MT
Zhang, SL
Crawford, DR
机构
[1] Albany Med Coll, Ctr Immunol & Microbial Dis, Albany, NY 12208 USA
[2] Ordway Res Inst, Stratton Affairs Med Ctr, Res Serv, Albany, NY 12206 USA
[3] New York State Dept Hlth, Wadsworth Ctr, Albany, NY 12206 USA
关键词
oxidative stress; nitrosative stress; calcineurin; protein stability; subcellular fractionation; stress-response; free radicals;
D O I
10.1016/j.freeradbiomed.2004.05.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Adapt78 is an oxidative and calcium stress-response gene. Its protein product is a potent natural inhibitor of the intracellular calcium signaling protein calcineurin. Much of what is known about Adapt78 protein is based on cell-transfection studies. Toward understanding natural endogenous Adapt78, we used an antibody raised against cellular Adapt78 and recently determined that endogenus Adapt78 protein, like its mRNA, is oxidative and calcium stress responsive. Here we report the identification of a second endogenous form of this protein family of 41 kDa. Subcellular fractionation of human HeLa cells revealed that in contrast to results of previous transfection studies, most endogenous Adapt78, characterized as 29 and 41 kDa electrophoretic doublets, resides in the cellular cytosol. The 41 kDa form of Adapt78 was abundant and found to exhibit many characteristics in common with the previously reported oxidative stress-responsive 29 kDa form, including hypo- and hyperphosphorylation variants, rapid loss of the hypophosphorylated form following oxidative stress, response to various kinase and phosphatase inhibitors, and localization. However, it also exhibited some unique characteristics, most notably the lack of calcium inducibility. Finally, the 29 kDa form exhibited a much shorter half-life and strong stabilization following oxidant exposure compared with the 41 kDa AdapF78 form. These data reveal the presence of a novel oxidative stress-responsive 41 kDa Adapt78 species, lend further insight into the Adapt78 family of proteins and their distribution, and challenge previous conclusions obtained using transfection protocols. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:454 / 462
页数:9
相关论文
共 36 条
[1]
Crawford Dana R., 1999, P155
[2]
CRAWFORD DR, 1994, METHODS ENZYMOL, V234, P175
[3]
ADAPTIVE RESPONSE AND OXIDATIVE STRESS [J].
CRAWFORD, DR ;
DAVIES, KJA .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1994, 102 :25-28
[4]
Hydrogen peroxide induces the expression of adapt15 a novel RNA associated with polysomes in hamster HA-1 cells [J].
Crawford, DR ;
Schools, GP ;
Salmon, SL ;
Davies, KJA .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1996, 325 (02) :256-264
[5]
Hamster adapt78 mRNA is a Down syndrome critical region homologue that is inducible by oxidative stress [J].
Crawford, DR ;
Leahy, KP ;
Abramova, N ;
Lan, L ;
Wang, YH ;
Davies, KJA .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 342 (01) :6-12
[6]
CRAWFORD DR, 1994, OXYGEN PARADOX, P327
[7]
Hydrogen peroxide-mediated phosphorylation of ERK1/2, Akt/PKB and JNK in cortical neurones:: dependence on Ca2+ and PI3-kinase [J].
Crossthwaite, AJ ;
Hasan, S ;
Williams, RJ .
JOURNAL OF NEUROCHEMISTRY, 2002, 80 (01) :24-35
[8]
Cunnick JM, 1998, BIOCHEM MOL BIOL INT, V45, P887
[9]
DSCR1, overexpressed in Down syndrome, is an inhibitor of calcineurin-mediated signaling pathways [J].
Fuentes, JJ ;
Genescà, L ;
Kingsbury, TJ ;
Cunningham, KW ;
Pérez-Riba, M ;
Estivill, X ;
de la Luna, S .
HUMAN MOLECULAR GENETICS, 2000, 9 (11) :1681-1690
[10]
Phosphorylation of calcipressin 1 increases its ability to inhibit calcineurin and decreases calcipressin half-life [J].
Genescà, L ;
Aubareda, A ;
Fuentes, JJ ;
Estivill, X ;
De la Luna, S ;
Pérez-Riba, M .
BIOCHEMICAL JOURNAL, 2003, 374 (02) :567-575