The manganese superoxide dismutase gene of Drosophila: Structure, expression, and evidence for regulation by MAP kinase

被引:39
作者
Duttaroy, A [1 ]
Parkes, T [1 ]
Emtage, P [1 ]
Kirby, K [1 ]
Boulianne, GL [1 ]
Wang, XD [1 ]
Hilliker, AJ [1 ]
Phillips, JP [1 ]
机构
[1] UNIV GUELPH, DEPT MOL BIOL & GENET, GUELPH, ON N1G 2W1, CANADA
关键词
D O I
10.1089/dna.1997.16.391
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
The gene encoding manganese superoxide dismutase (MnSOD) from Drosophila melanogaster has been isolated and its expression has been studied. In contrast to several mammalian MnSOD genes, the Drosophila gene contains a single intron and is transcribed into a single 0.8-kb transcript. Whole-mount in situ hybridization reveals extensive transcript accumulation in ovarian nurse cells and a heavy maternal contribution to the early embryo, Larval imaginal discs are enriched with MnSOD transcripts relative to other larval tissues, further suggesting a possible relationship between high MnSOD expression and mitotic activity. The 5'-upstream region contains several well-known regulatory elements including metal response, antioxidant response, and xenobiotic response elements (MRE, ARE, and XRE, respectively), sites for activator protein-1 (AP-1), nuclear factor-kappa B (NF-kappa B), adenosine 3',5'-cyclic monophosphate regulator binding element factor (CREB), as well as classic TATA and CAAT boxes. That MnSOD expression in Drosophila is regulated in part by the transcription factor AP-1 via the MAP kinase signal transduction pathway is suggested by experiments which show that a hypomorphic mutation of the MAP kinase-encoding rolled gene substantially reduces levels of MnSOD transcripts and correlates with reduced resistance to oxidative stress in rolled mutants.
引用
收藏
页码:391 / 399
页数:9
相关论文
共 47 条
[1]   MITOCHONDRIAL-DNA DEFECTS IN DIABETES-MELLITUS [J].
ALCOLADO, JC .
DIABETOLOGIA, 1993, 36 (06) :578-578
[2]   MITOCHONDRIAL DECAY IN AGING [J].
AMES, BN ;
SHIGENAGA, MK ;
HAGEN, TM .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1995, 1271 (01) :165-170
[3]   DELETERIOUS MITOCHONDRIAL-DNA MUTATIONS ACCUMULATE IN AGING HUMAN TISSUES [J].
ARNHEIM, N ;
CORTOPASSI, G .
MUTATION RESEARCH, 1992, 275 (3-6) :157-167
[4]  
Ashburner M., 1989, DROSOPHILA LAB MANUA
[5]   RHOMBOID, A GENE REQUIRED FOR DORSOVENTRAL AXIS ESTABLISHMENT AND PERIPHERAL NERVOUS-SYSTEM DEVELOPMENT IN DROSOPHILA-MELANOGASTER [J].
BIER, E ;
JAN, LY ;
JAN, YN .
GENES & DEVELOPMENT, 1990, 4 (02) :190-203
[6]   THE DROSOPHILA ROLLED LOCUS ENCODES A MAP KINASE REQUIRED IN THE SEVENLESS SIGNAL-TRANSDUCTION PATHWAY [J].
BIGGS, WH ;
ZAVITZ, KH ;
DICKSON, B ;
VANDERSTRATEN, A ;
BRUNNER, D ;
HAFEN, E ;
ZIPURSKY, SL .
EMBO JOURNAL, 1994, 13 (07) :1628-1635
[7]   MOBILIZATION OF HOBO ELEMENTS RESIDING WITHIN THE DECAPENTAPLEGIC GENE-COMPLEX - SUGGESTION OF A NEW HYBRID DYSGENESIS SYSTEM IN DROSOPHILA-MELANOGASTER [J].
BLACKMAN, RK ;
GRIMAILA, R ;
KOEHLER, MMD ;
GELBART, WM .
CELL, 1987, 49 (04) :497-505
[8]   OXIDANT CARCINOGENESIS AND ANTIOXIDANT DEFENSE [J].
CERUTTI, P ;
SHAH, G ;
PESKIN, A ;
AMSTAD, P .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES-SERIES, 1992, 663 :158-166
[9]   INCREASED MANGANESE SUPEROXIDE-DISMUTASE EXPRESSION SUPPRESSES THE MALIGNANT PHENOTYPE OF HUMAN-MELANOMA CELLS [J].
CHURCH, SL ;
GRANT, JW ;
RIDNOUR, LA ;
OBERLEY, LW ;
SWANSON, PE ;
MELTZER, PS ;
TRENT, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :3113-3117
[10]   MODELING THE EFFECTS OF AGE-RELATED MTDNA MUTATION ACCUMULATION - COMPLEX-I DEFICIENCY, SUPEROXIDE AND CELL-DEATH [J].
CORTOPASSI, G ;
WANG, E .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1995, 1271 (01) :171-176