Inhibition of cell growth and apoptosis by inducible expression of the transcriptional repressor Mad1

被引:24
作者
Bejarano, MT [1 ]
Albihn, A [1 ]
Cornvik, T [1 ]
Brijker, SO [1 ]
Asker, C [1 ]
Osorio, LM [1 ]
Henriksson, M [1 ]
机构
[1] Karolinska Inst, Microbiol & Tumor Biol Ctr, S-17177 Stockholm, Sweden
关键词
Mad1; cell growth; cell cycle; apoptosis;
D O I
10.1006/excr.2000.4996
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mad1 is a Myc antagonist that heterodimerizes with Max and functions as a transcriptional repressor. We have studied the effects of Mad1 on cell growth, cell cycle distribution, and apoptosis using Mad1-inducible cell lines. Expression of Mad1 inhibited cell proliferation, S-phase entry, and colony formation, changes that were accompanied by a reduction in CDK2 activity. The inhibition of Mad1 on cell proliferation was potentiated by serum starvation and was paralleled by accumulation of cells in the G0/G1 and the G2 phases of the cell cycle. Mad1 also reduced apoptosis induced by serum withdrawal and by the cytostatic drug cisplatinum. The effects on both cell growth and apoptosis were dependent on the mSin3 interaction domain of Mad1, which is necessary for recruitment of histone deacetylases and corepressors, suggesting that transcriptional repression is mediating these functions. Taken together with the expression pattern of Mad1, these results suggest that Mad1 plays an important role during initiation of differentiation by inhibiting cell proliferation and blocking apoptosis. (C) 2000 Academic Press.
引用
收藏
页码:61 / 72
页数:12
相关论文
共 62 条
[1]   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
[2]  
Amati B., 1998, FRONT BIOSCI, V3, pd250, DOI DOI 10.2741/A239
[3]  
Ayer DE, 1996, MOL CELL BIOL, V16, P5772
[4]   MAD-MAX TRANSCRIPTIONAL REPRESSION IS MEDIATED BY TERNARY COMPLEX-FORMATION WITH MAMMALIAN HOMOLOGS OF YEAST REPRESSOR SIN3 [J].
AYER, DE ;
LAWRENCE, QA ;
EISENMAN, RN .
CELL, 1995, 80 (05) :767-776
[5]   MAD - A HETERODIMERIC PARTNER FOR MAX THAT ANTAGONIZES MYC TRANSCRIPTIONAL ACTIVITY [J].
AYER, DE ;
KRETZNER, L ;
EISENMAN, RN .
CELL, 1993, 72 (02) :211-222
[6]   A SWITCH FROM MYC-MAX TO MAD-MAX HETEROCOMPLEXES ACCOMPANIES MONOCYTE/MACROPHAGE DIFFERENTIATION [J].
AYER, DE ;
EISENMAN, RN .
GENES & DEVELOPMENT, 1993, 7 (11) :2110-2119
[7]   Repression of c-Myc responsive genes in cycling cells causes G(1) arrest through reduction of cyclin E CDK2 kinase activity [J].
Berns, K ;
Hijmans, EM ;
Bernards, R .
ONCOGENE, 1997, 15 (11) :1347-1356
[8]   APOPTOTIC CELL-DEATH INDUCED BY C-MYC IS INHIBITED BY BCL-2 [J].
BISSONNETTE, RP ;
ECHEVERRI, F ;
MAHBOUBI, A ;
GREEN, DR .
NATURE, 1992, 359 (6395) :552-554
[9]  
CERNI C, 1995, ONCOGENE, V11, P587
[10]   HIGH-EFFICIENCY TRANSFORMATION OF MAMMALIAN-CELLS BY PLASMID DNA [J].
CHEN, C ;
OKAYAMA, H .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (08) :2745-2752