THE TRANSCRIPTIONAL FACTOR EGR-1 IS SYNTHESIZED BY BACULOVIRUS-INFECTED INSECT CELLS IN AN ACTIVE, DNA-BINDING FORM

被引:15
作者
RAGONA, G
EDWARDS, SA
MERCOLA, DA
ADAMSON, ED
CALOGERO, A
机构
[1] LA JOLLA CANC RES FDN, 10901 N TORREY PINES RD, LA JOLLA, CA 92037 USA
[2] UNIV ROME, DEPT EXPTL MED, I-00161 ROME, ITALY
[3] VET ADM MED CTR, PATHOL RES SERV, SAN DIEGO, CA 92161 USA
[4] VET ADM MED CTR, DEPT PATHOL, SAN DIEGO, CA 92161 USA
[5] UNIV AQUILA, DEPT CLIN PATHOL, ROME, ITALY
关键词
D O I
10.1089/dna.1991.10.61
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 Egr-1 (zfp-6) gene encodes a zinc-finger-containing nuclear protein that is rapidly and transiently induced in quiescent cells treated with mitogens. We have constructed baculovirus vectors that synthesize mouse Egr-1 protein initiating at two putative ATG start sites. The ATG site producing the larger protein (M(r), 80,000) is similar, if not identical, to Egr-1 synthesized by serum-stimulated quiescent mouse fibroblasts, thus identifying the likely site for translation. The protein synthesized by the insect cells is active as assayed by its ability to bind to a specific DNA sequence that has been identified as an Egr-1 binding site. The insect cell system will allow further studies of the structure and function of the Egr-1 product, a protein that appears to be an important "master switch" for other genes.
引用
收藏
页码:61 / 66
页数:6
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