ROLE OF E2F TRANSCRIPTION FACTOR IN E1A-MEDIATED TRANSACTIVATION OF CELLULAR GENES

被引:128
作者
HIEBERT, SW [1 ]
BLAKE, M [1 ]
AZIZKHAN, J [1 ]
NEVINS, JR [1 ]
机构
[1] UNIV N CAROLINA, LINEBERGER COMPREHENS CANC CTR, CHAPEL HILL, NC 27599 USA
关键词
D O I
10.1128/JVI.65.7.3547-3552.1991
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Adenovirus E1A-dependent trans activation of the adenovirus E2 gene involves the activation of the cellular transcription factor E2F. E2F binding sites have also been identified in the 5'-flanking region of a number of cellular genes, raising the possibility that such genes are targets for E1A trans activation. We now demonstrate that two genes that posses E2F recognition sites, N-myc and DHFR, are stimulated by E1A, dependent on the E2F sites. We also find that although there are multiple E2F sites in these promoters, a single intact E2F binding site is sufficient for E1A-mediated induction, although not to the full wild-type level. These results thus demonstrate that a variety of cellular genes that possess E2F binding sites are subject to E1A trans activation. Moreover, since the products of most of these genes are likely critical for cellular proliferation, there are obvious consequences of this trans activation for cellular phenotype.
引用
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页码:3547 / 3552
页数:6
相关论文
共 31 条
[1]   ADENOVIRUS E1A PROTEINS CAN DISSOCIATE HETEROMERIC COMPLEXES INVOLVING THE E2F TRANSCRIPTION FACTOR - A NOVEL MECHANISM FOR E1A TRANSACTIVATION [J].
BAGCHI, S ;
RAYCHAUDHURI, P ;
NEVINS, JR .
CELL, 1990, 62 (04) :659-669
[2]   PHOSPHORYLATION-DEPENDENT ACTIVATION OF THE ADENOVIRUS-INDUCIBLE E2F TRANSCRIPTION FACTOR IN A CELL-FREE SYSTEM [J].
BAGCHI, S ;
RAYCHAUDHURI, P ;
NEVINS, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (12) :4352-4356
[3]   TRANSCRIPTION FACTOR E2F IS REQUIRED FOR EFFICIENT EXPRESSION OF THE HAMSTER DIHYDROFOLATE-REDUCTASE GENE INVITRO AND INVIVO [J].
BLAKE, MC ;
AZIZKHAN, JC .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (11) :4994-5002
[4]   TRANSACTIVATION OF HUMAN-IMMUNODEFICIENCY-VIRUS OCCURS VIA A BIMODAL MECHANISM [J].
CULLEN, BR .
CELL, 1986, 46 (07) :973-982
[5]   STRUCTURE AND EXPRESSION OF THE MURINE N-MYC GENE [J].
DEPINHO, RA ;
LEGOUY, E ;
FELDMAN, LB ;
KOHL, NE ;
YANCOPOULOS, GD ;
ALT, FW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (06) :1827-1831
[6]   E1A 13S AND 12S MESSENGER-RNA PRODUCTS MADE IN ESCHERICHIA-COLI BOTH FUNCTION AS NUCLEUS-LOCALIZED TRANSCRIPTION ACTIVATORS BUT DO NOT DIRECTLY BIND DNA [J].
FERGUSON, B ;
KRIPPL, B ;
ANDRISANI, O ;
JONES, N ;
WESTPHAL, H ;
ROSENBERG, M .
MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (10) :2653-2661
[7]   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
[8]   AN ADENOVIRUS EARLY REGION-4 GENE-PRODUCT IS REQUIRED FOR INDUCTION OF THE INFECTION-SPECIFIC FORM OF CELLULAR E2F ACTIVITY [J].
HARDY, S ;
ENGEL, DA ;
SHENK, T .
GENES & DEVELOPMENT, 1989, 3 (07) :1062-1074
[9]   E1A-DEPENDENT TRANS-ACTIVATION OF THE HUMAN MYC PROMOTER IS MEDIATED BY THE E2F FACTOR [J].
HIEBERT, SW ;
LIPP, M ;
NEVINS, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (10) :3594-3598
[10]   ADENOVIRUS EARLY REGION-4 ENCODES 2 GENE-PRODUCTS WITH REDUNDANT EFFECTS IN LYTIC INFECTION [J].
HUANG, MM ;
HEARING, P .
JOURNAL OF VIROLOGY, 1989, 63 (06) :2605-2615