Expression of MXI1, a Myc antagonist, is regulated by Sp1 and AP2

被引:31
作者
Benson, LQ [1 ]
Coon, MR [1 ]
Krueger, LM [1 ]
Han, GC [1 ]
Sarnaik, AA [1 ]
Wechsler, DS [1 ]
机构
[1] Univ Michigan, Div Pediat Hematol Oncol, Dept Pediat & Communicable Dis, Sch Med, Ann Arbor, MI 48109 USA
关键词
D O I
10.1074/jbc.274.40.28794
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
MXI1, a member of the MAD family of Myc antagonists, encodes a transcription factor whose expression must be tightly regulated to maintain normal cell growth and differentiation. To more closely investigate the transcriptional regulation of the human MXI1 gene, we have cloned and characterized the MXI1 promoter. After clarification of the 5'- and 3'-untranslated regions of the cDNA (indicating that the true length of the MXI1 transcript is 2643 base pairs), we identified two transcription initiation sites. We subsequently isolated the MXI1 promoter, which is GC-rich and lacks a TATA box. Although it contains at least six potential initiator sequences, functional studies indicate the proximal two initiator sequences in combination with nearby Spl and MED-1 sites together account for virtually all promoter activity. We also demonstrate that MXI1 promoter activity is repressed by high levels of AP2. These studies provide further insight into the complex regulatory mechanisms governing MXI1 gene expression and its role in cellular differentiation and tumor suppression.
引用
收藏
页码:28794 / 28802
页数:9
相关论文
共 61 条
[1]  
ALBAROSA R, 1995, HUM GENET, V95, P709
[2]   Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression [J].
Alland, L ;
Muhle, R ;
Hou, H ;
Potes, J ;
Chin, L ;
SchreiberAgus, N ;
DePinho, RA .
NATURE, 1997, 387 (6628) :49-55
[3]   MAD - A HETERODIMERIC PARTNER FOR MAX THAT ANTAGONIZES MYC TRANSCRIPTIONAL ACTIVITY [J].
AYER, DE ;
KRETZNER, L ;
EISENMAN, RN .
CELL, 1993, 72 (02) :211-222
[4]  
Azizkhan Jane C., 1993, Critical Reviews in Eukaryotic Gene Expression, V3, P229
[5]   A TATA-LESS PROMOTER CONTAINING BINDING-SITES FOR UBIQUITOUS TRANSCRIPTION FACTORS MEDIATES CELL-TYPE-SPECIFIC REGULATION OF THE GENE FOR TRANSCRIPTION ENHANCER FACTOR-I (TEF-1) [J].
BOAM, DSW ;
DAVIDSON, I ;
CHAMBON, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (33) :19487-19494
[6]   Control of cell proliferation by Myc [J].
Bouchard, C ;
Staller, P ;
Eilers, M .
TRENDS IN CELL BIOLOGY, 1998, 8 (05) :202-206
[7]   PURIFICATION AND BIOCHEMICAL-CHARACTERIZATION OF THE PROMOTER-SPECIFIC TRANSCRIPTION FACTOR, SPL [J].
BRIGGS, MR ;
KADONAGA, JT ;
BELL, SP ;
TJIAN, R .
SCIENCE, 1986, 234 (4772) :47-52
[8]   ALLELIC LOSS OF CHROMOSOME-16Q AND CHROMOSOME-10Q IN HUMAN PROSTATE-CANCER [J].
CARTER, BS ;
EWING, CM ;
WARD, WS ;
TREIGER, BF ;
AALDERS, TW ;
SCHALKEN, JA ;
EPSTEIN, JI ;
ISAACS, WB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (22) :8751-8755
[9]   Regulation of K3 keratin gene transcription by Sp1 and AP-2 in differentiating rabbit corneal epithelial cells [J].
Chen, TT ;
Wu, RL ;
CastroMunozledo, F ;
Sun, TT .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (06) :3056-3064
[10]  
Dang CV, 1999, MOL CELL BIOL, V19, P1