DSCR1 (Adapt78) modulates expression of SOD1

被引:29
作者
Ermak, G
Cheadle, C
Becker, KG
Harris, CD
Davies, KJA
机构
[1] Univ So Calif, Ethel Percy Andrus Gerontol Ctr, Los Angeles, CA 90089 USA
[2] Univ So Calif, Div Mol & Computat Biol, Los Angeles, CA 90089 USA
[3] NIA, DNA Array Unit, Res Resources Branch, NIH, Baltimore, MD 21224 USA
关键词
calcipressin; 1; sod; oxidative stress; Down's syndrome;
D O I
10.1096/fj.03-0451com
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
DSCR1(Adapt78) is a stress responsive gene that can be induced by multiple stresses. We have previously demonstrated that acute DSCR1(Adapt78) overexpression can transiently protect cells against oxidative stress and calcium-mediated stresses, while its chronic overexpression is associated with neurofibrillary tangles, Alzheimer disease, and Down's syndrome. It seems that a delicate balance of DSCR1(Adapt78) expression is maintained in cells, and this gene can have either protective or damaging effects, depending on both its level and duration of expression. The mechanisms by which DSCR1(Adapt78) can protect or harm cells are poorly understood. Here, we tried to identify pathways and targets affected by the DSCR1(Adapt78) gene using regulated expression of DSCR1(Adapt78) in PC-12 cells, followed by microarray analysis of mRNAs from these cells. We found that DSCR1(Adapt78) expression stimulates SOD1 (intracellular Cu,Zn superoxide dismutase) gene expression and increased sod 1 enzyme activity. Previous studies have indicated that sod 1 can either protect or damage cells, depending on its levels. Our findings suggest that sod 1 may also be involved in both the acute protective and the chronic damaging effects of DSCR1(Adapt78) expression. These data also have importance for our understanding of Down's syndrome, Alzheimer's disease, and other human pathologies.
引用
收藏
页码:62 / 69
页数:8
相关论文
共 43 条
  • [1] LIPID-PEROXIDATION AND SUPEROXIDE DISMUTASE-1 AND GLUTATHIONE-PEROXIDASE ACTIVITIES IN TRISOMY-16 FETAL MICE AND HUMAN TRISOMY-21 FIBROBLASTS
    ANNEREN, KG
    EPSTEIN, CJ
    [J]. PEDIATRIC RESEARCH, 1987, 21 (01) : 88 - 92
  • [2] High level calcineurin activity predisposes neuronal cells to apoptosis
    Asai, A
    Qiu, JH
    Narita, Y
    Chi, S
    Saito, N
    Shinoura, N
    Hamada, H
    Kuchino, Y
    Kirino, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (48) : 34450 - 34458
  • [3] Barrett T, 2001, RESTOR NEUROL NEUROS, V18, P127
  • [4] SUPEROXIDE-DISMUTASE, GLUTATHIONE-PEROXIDASE AND LIPOPEROXIDATION IN DOWNS-SYNDROME FETAL BRAIN
    BROOKSBANK, BWL
    BALAZS, R
    [J]. DEVELOPMENTAL BRAIN RESEARCH, 1984, 16 (01): : 37 - 44
  • [5] APOPTOSIS AND INCREASED GENERATION OF REACTIVE OXYGEN SPECIES IN DOWNS-SYNDROME NEURONS IN-VITRO
    BUSCIGLIO, J
    YANKNER, BA
    [J]. NATURE, 1995, 378 (6559) : 776 - 779
  • [6] CEBALLOS I, 1991, FREE RADICAL RES COM, V12-3, P571
  • [7] Analysis of microarray data using Z score transformation
    Cheadle, C
    Vawter, MP
    Freed, WJ
    Becker, KG
    [J]. JOURNAL OF MOLECULAR DIAGNOSTICS, 2003, 5 (02) : 73 - 81
  • [8] A calcineurin-dependent transcriptional pathway controls skeletal muscle fiber type
    Chin, ER
    Olson, EN
    Richardson, JA
    Yano, Q
    Humphries, C
    Shelton, JM
    Wu, H
    Zhu, WG
    Bassel-Duby, R
    Williams, RS
    [J]. GENES & DEVELOPMENT, 1998, 12 (16) : 2499 - 2509
  • [9] IDENTIFICATION OF CALCINEURIN AS A KEY SIGNALING ENZYME IN LYMPHOCYTE-T ACTIVATION
    CLIPSTONE, NA
    CRABTREE, GR
    [J]. NATURE, 1992, 357 (6380) : 695 - 697
  • [10] Hamster adapt78 mRNA is a Down syndrome critical region homologue that is inducible by oxidative stress
    Crawford, DR
    Leahy, KP
    Abramova, N
    Lan, L
    Wang, YH
    Davies, KJA
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 342 (01) : 6 - 12