VARGULA-HILGENDORFII LUCIFERASE - A SECRETED REPORTER ENZYME FOR MONITORING GENE-EXPRESSION IN MAMMALIAN-CELLS

被引:56
作者
THOMPSON, EM
NAGATA, S
TSUJI, FI
机构
[1] OSAKA BIOSCI INST,6-2-4 FURUEDAI,SUITA,OSAKA 565,JAPAN
[2] UNIV CALIF SAN DIEGO,SCRIPPS INST OCEANOG,DIV MARINE BIOL RES,LA JOLLA,CA 92093
基金
日本科学技术振兴机构; 美国国家科学基金会;
关键词
bioluminescence; CAT assay; eukaryotic expression vectors; gene regulation; Recombinant DNA; transfection;
D O I
10.1016/0378-1119(90)90261-O
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The small marine ostracod crustacean, Vargula hilgendorfii, produces a brigth blue luminous secretion which is ejected into seawater. The luminescence is due to a simple enzyme-catalyzed reaction involving only luciferase, luciferin (substrate), and molecular oxygen. Thus, V. hilgendorfii luciferase (VL) should be useful as a reporter enzyme in studies of gene expression in mammalian cells. Expression plasmids consisting of VL cDNA (vl) linked to the promoters simian virus 40 early region, Rous sarcoma virus long terminal repeat, human elongation factor, or mouse granulocyte colony-stimulating factor were introduced into a series of mammalian cell lines. Following transfection, VL activities in cell extracts and culture media were determine by a rapid ligh emission assay with V. hilgendorfii luciferin. Parallel experiments were carried out with the chloramphenicol acetyltransferase (CAT)-encoding gene. In all cell lines tested, VL was secreted, allowing the reporter activity to be determined directly from a small aliquot of the culture medium. The results indicate that the secreted VL enzyme is superior to CAT, firefly luciferase, and bacterial luciferase as a convenient and versatile indicator of gene expression in mammalian cells. © 1990.
引用
收藏
页码:257 / 262
页数:6
相关论文
共 36 条
[1]   STEROID-RECEPTOR MEDIATED INHIBITION OF RAT PROLACTIN GENE-EXPRESSION DOES NOT REQUIRE THE RECEPTOR DNA-BINDING DOMAIN [J].
ADLER, S ;
WATERMAN, ML ;
XI, H ;
ROSENFELD, MG .
CELL, 1988, 52 (05) :685-695
[2]   EXPRESSION OF BACTERIAL BETA-GALACTOSIDASE IN ANIMAL-CELLS [J].
AN, GH ;
HIDAKA, K ;
SIMINOVITCH, L .
MOLECULAR AND CELLULAR BIOLOGY, 1982, 2 (12) :1628-1632
[3]   SECRETED PLACENTAL ALKALINE-PHOSPHATASE - A POWERFUL NEW QUANTITATIVE INDICATOR OF GENE-EXPRESSION IN EUKARYOTIC CELLS [J].
BERGER, J ;
HAUBER, J ;
HAUBER, R ;
GEIGER, R ;
CULLEN, BR .
GENE, 1988, 66 (01) :1-10
[4]  
BOYLAN M, 1989, J BIOL CHEM, V264, P1915
[5]  
BUCHMAN AR, 1981, DNA TUMOR VIRUSES 2, P799
[6]   RAPID ASSAY FOR DETECTION OF ESCHERICHIA-COLI XANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE ACTIVITY IN TRANSDUCED CELLS [J].
CHU, G ;
BERG, P .
NUCLEIC ACIDS RESEARCH, 1985, 13 (08) :2921-2930
[7]   FIREFLY LUCIFERASE GENE - STRUCTURE AND EXPRESSION IN MAMMALIAN-CELLS [J].
DEWET, JR ;
WOOD, KV ;
DELUCA, M ;
HELINSKI, DR ;
SUBRAMANI, S .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (02) :725-737
[8]   UTILITY OF FIREFLY LUCIFERASE AS A REPORTER GENE FOR PROMOTER ACTIVITY IN TRANSGENIC MICE [J].
DILELLA, AG ;
HOPE, DA ;
CHEN, H ;
TRUMBAUER, M ;
SCHWARTZ, RJ ;
SMITH, RG .
NUCLEIC ACIDS RESEARCH, 1988, 16 (09) :4159-4159
[9]   INSITU DETECTION OF BETA-GALACTOSIDASE IN LENSES OF TRANSGENIC MICE WITH A GAMMA-CRYSTALLIN-LACZ GENE [J].
GORING, DR ;
ROSSANT, J ;
CLAPOFF, S ;
BREITMAN, ML ;
TSUI, LC .
SCIENCE, 1987, 235 (4787) :456-458
[10]  
Gorman C., 1985, DNA CLONING PRACTICA, V1, P143