PUF/NM23-H2/NDPK-B TRANSACTIVATES A HUMAN C-MYC PROMOTER-CAT GENE VIA A FUNCTIONAL NUCLEASE HYPERSENSITIVE ELEMENT

被引:0
作者
BERBERICH, SJ [1 ]
POSTEL, EH [1 ]
机构
[1] PRINCETON UNIV, DEPT MOLEC BIOL, PRINCETON, NJ 08544 USA
关键词
PUF; NM23; NDPK; C-MYC; NUCLEASE HYPERSENSITIVE METASTASIS;
D O I
暂无
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 isolated the transacting factor PuF that, through its interaction with a nuclease hypersensitive element (NHE) located upstream of the c-myc gene, transactivates the human c-myc gene in vitro (Postel et al., 1989). PuF was recently identified as being encoded by the nonmetastatic 23-H2 (nm23-H2)/nucleoside diphosphate kinase-B (NDPK-B) gene (Postel ct al., 1993). In addition to its ability to transactivate the c-myc gene in vitro, PuF/NDPK-B catalyzes the shuttling of gamma-phosphates between nucleoside triphosphates and diphosphates (Gilles et al., 1991; Postel and Ferrone, 1994) and has been postulated to suppress tumor metastasis (Stahl et al., 1991). Here we have extended our studies of PuF and c-myc transcription by testing whether PuF affects c-myc transcription using a transient transfection assay. A plasmid containing the human c-myc promoter-NHE region was cloned upstream of the bacterial chloramphenicol acetyltransferase (CAT) gene. When cotransfected with a PuF expression vector, CAT activity was elevated 3-4 fold relative to transfections containing the myc-CAT plasmid. In contrast, a myc-CAT reporter plasmid in which the NHE element was deleted showed no increase in CAT activity when cotransfected with the PuF expression vector. From these results we conclude that PuF transactivates the c-myc gene via the nuclease hypersensitive element.
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页码:2343 / 2347
页数:5
相关论文
共 31 条
[1]  
ARCINAS M, 1994, ONCOGENE, V9, P2699
[2]  
AVIGAN MI, 1990, J BIOL CHEM, V265, P18538
[3]  
BEVILACQUA G, 1989, CANCER RES, V49, P5185
[4]   A DROSOPHILA GENE THAT IS HOMOLOGOUS TO A MAMMALIAN GENE ASSOCIATED WITH TUMOR-METASTASIS CODES FOR A NUCLEOSIDE DIPHOSPHATE KINASE [J].
BIGGS, J ;
HERSPERGER, E ;
STEEG, PS ;
LIOTTA, LA ;
SHEARN, A .
CELL, 1990, 63 (05) :933-940
[5]   DNA-STRUCTURE EQUILIBRIA IN THE HUMAN C-MYC GENE [J].
BOLES, TC ;
HOGAN, ME .
BIOCHEMISTRY, 1987, 26 (02) :367-376
[6]   THE MYC ONCOGENE - ITS ROLE IN TRANSFORMATION AND DIFFERENTIATION [J].
COLE, MD .
ANNUAL REVIEW OF GENETICS, 1986, 20 :361-384
[7]   SITE-SPECIFIC OLIGONUCLEOTIDE BINDING REPRESSES TRANSCRIPTION OF THE HUMAN C-MYC GENE INVITRO [J].
COONEY, M ;
CZERNUSZEWICZ, G ;
POSTEL, EH ;
FLINT, SJ ;
HOGAN, ME .
SCIENCE, 1988, 241 (4864) :456-459
[8]   C-MYC ONCOPROTEIN FUNCTION [J].
DANG, CV .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :103-113
[9]   RIBONUCLEOPROTEIN AND PROTEIN FACTORS BIND TO AN H-DNA-FORMING C-MYC DNA ELEMENT - POSSIBLE REGULATORS OF THE C-MYC GENE [J].
DAVIS, TL ;
FIRULLI, AB ;
KINNIBURGH, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) :9682-9686
[10]   SEQUENCE-SPECIFIC, SINGLE-STRAND BINDING-PROTEIN ACTIVATES THE FAR UPSTREAM ELEMENT OF C-MYC AND DEFINES A NEW DNA-BINDING MOTIF [J].
DUNCAN, R ;
BAZAR, L ;
MICHELOTTI, G ;
TOMONAGA, T ;
KRUTZSCH, H ;
AVIGAN, M ;
LEVENS, D .
GENES & DEVELOPMENT, 1994, 8 (04) :465-480