SYNERGISTIC INDUCTION OF PROMOTERS CONTAINING METAL-RESPONSIVE AND GLUCOCORTICOID-RESPONSIVE ELEMENTS

被引:14
作者
FILMUS, J
REMANI, J
KLEIN, MH
机构
[1] SUNNYBROOK HLTH SCI CTR, DIV CANC RES,REICHMANN RES BLDG,S-218, 2075 BAYVIEW AVE, TORONTO M4N 3M5, ONTARIO, CANADA
[2] CONNAUGHT CTR BIOTECHNOL RES, N YORK M2R 3T4, ONTARIO, CANADA
关键词
D O I
10.1093/nar/20.11.2755
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
We have shown that it is possible to synergistically activate gene transcription when several glucocorticoid responsive elements (GREs) and metal responsive elements (MREs) that coexist within the same promoter are induced simultaneously. To demonstrate this, additional GREs were introduced into a human metallothionein IIA (hMT-IIA) promoter in which some constitutive elements had been deleted. The transcriptional strength and inducibility of the modified hMT-IIA promoters were studied in transient expression experiments using the CAT gene as a reporter. As a result of synergistic activation of transcription by CdCl2 and dexamethasone, the induced expression levels of the modified promoters were significantly higher than those obtained with wild-type hMT-IIA. Since the increase in inducible expression was not accompanied by a concominant increase in basal levels, the inducibility of the modified MT promoters was up to 6-fold higher. The degree of transcriptional synergism was shown to depend on the position and the number of GREs introduced. Thus, the engineering of synthetic promoters that include both GREs and MREs should offer the opportunity to develop a new series of improved inducible mammalian expression vectors.
引用
收藏
页码:2755 / 2760
页数:6
相关论文
共 36 条
[1]   STEROID-HORMONE RECEPTORS AND INVITRO TRANSCRIPTION [J].
ALLAN, GF ;
TSAI, SY ;
OMALLEY, BW ;
TSAI, MJ .
BIOESSAYS, 1991, 13 (02) :73-78
[2]   COOPERATIVE BINDING OF THE GLUCOCORTICOID RECEPTOR DNA-BINDING DOMAIN IS ONE OF AT LEAST 2 MECHANISMS FOR SYNERGISM [J].
BANIAHMAD, C ;
MULLER, M ;
ALTSCHMIED, J ;
RENKAWITZ, R .
JOURNAL OF MOLECULAR BIOLOGY, 1991, 222 (02) :155-165
[3]   TRANSCRIPTIONAL CONTROL BY NUCLEAR RECEPTORS [J].
BEATO, M .
FASEB JOURNAL, 1991, 5 (07) :2044-2051
[4]   GENE-REGULATION BY STEROID-HORMONES [J].
BEATO, M .
CELL, 1989, 56 (03) :335-344
[5]   UBIQUITOUS TRANSCRIPTION FACTOR OTF-1 MEDIATES INDUCTION OF THE MMTV PROMOTER THROUGH SYNERGISTIC INTERACTION WITH HORMONE RECEPTORS [J].
BRUGGEMEIER, U ;
KALFF, M ;
FRANKE, S ;
SCHEIDEREIT, C ;
BEATO, M .
CELL, 1991, 64 (03) :565-572
[6]   A MECHANISM FOR SYNERGISTIC ACTIVATION OF A MAMMALIAN GENE BY GAL4 DERIVATIVES [J].
CAREY, M ;
LIN, YS ;
GREEN, MR ;
PTASHNE, M .
NATURE, 1990, 345 (6273) :361-364
[7]   ALPHA-INTERFERON-INDUCED TRANSCRIPTION OF HLA AND METALLOTHIONEIN GENES CONTAINING HOMOLOGOUS UPSTREAM SEQUENCES [J].
FRIEDMAN, RL ;
STARK, GR .
NATURE, 1985, 314 (6012) :637-639
[8]   FUNCTIONAL DOMAINS OF THE HUMAN GLUCOCORTICOID RECEPTOR [J].
GIGUERE, V ;
HOLLENBERG, SM ;
ROSENFELD, MG ;
EVANS, RM .
CELL, 1986, 46 (05) :645-652
[9]   RECOMBINANT GENOMES WHICH EXPRESS CHLORAMPHENICOL ACETYLTRANSFERASE IN MAMMALIAN-CELLS [J].
GORMAN, CM ;
MOFFAT, LF ;
HOWARD, BH .
MOLECULAR AND CELLULAR BIOLOGY, 1982, 2 (09) :1044-1051
[10]   NEW TECHNIQUE FOR ASSAY OF INFECTIVITY OF HUMAN ADENOVIRUS 5 DNA [J].
GRAHAM, FL ;
VANDEREB, AJ .
VIROLOGY, 1973, 52 (02) :456-467