The Myc/Max/Mad network and the transcriptional control of cell behavior

被引:1038
作者
Grandori, C
Cowley, SM
James, LP
Eisenman, RN
机构
[1] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
[2] Univ Washington, Mol & Cellular Biol Program, Seattle, WA 98195 USA
关键词
transcription; repression; cell cycle; oncogene;
D O I
10.1146/annurev.cellbio.16.1.653
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Myc/Max/Mad network comprises a group of transcription factors whose distinct interactions result in gene-specific transcriptional activation or repression. A great deal of research indicates that the functions of the network play roles in cell proliferation, differentiation, and death. In this review we focus on the Myc and Mad protein families and attempt to relate their biological functions to their transcriptional activities and gene targets. Both Myc and Mad, as well as the more recently described Mnt and Mga proteins, form heterodimers with Max, permitting binding to specific DNA sequences. These DNA-bound heterodimers recruit coactivator or corepressor complexes that generate alterations in chromatin structure, which in turn modulate transcription. Initial identification of target genes suggests that the network regulates genes involved in the cell cycle, growth, life span, and morphology. Because Myc and Mad proteins are expressed in response to diverse signaling pathways, the network can be viewed as a functional module which acts to convert environmental signals into specific gene-regulatory programs.
引用
收藏
页码:653 / 699
页数:51
相关论文
共 301 条
  • [81] Transient excess of MYC activity can elicit genomic instability and tumorigenesis
    Felsher, DW
    Bishop, JM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (07) : 3940 - 3944
  • [82] RECOGNITION BY MAX OF ITS COGNATE DNA THROUGH A DIMERIC B/HLH/Z DOMAIN
    FERREDAMARE, AR
    PRENDERGAST, GC
    ZIFF, EB
    BURLEY, SK
    [J]. NATURE, 1993, 363 (6424) : 38 - 45
  • [83] STRUCTURE AND FUNCTION OF THE B/HLH/Z DOMAIN OF USF
    FERREDAMARE, AR
    POGNONEC, P
    ROEDER, RG
    BURLEY, SK
    [J]. EMBO JOURNAL, 1994, 13 (01) : 180 - 189
  • [84] TRANSCRIPTION ACTIVATION BY MYC AND MAX - FLANKING SEQUENCES TARGET ACTIVATION TO A SUBSET OF CACGTG MOTIFS IN-VIVO
    FISHER, F
    CROUCH, DH
    JAYARAMAN, PS
    CLARK, W
    GILLESPIE, DAF
    GODING, CR
    [J]. EMBO JOURNAL, 1993, 12 (13) : 5075 - 5082
  • [85] Differential effects of the widely expressed dMax splice variant of Max on E-box vs initiator element-mediated regulation by c-Myc
    FitzGerald, MJ
    Arsura, M
    Bellas, RE
    Yang, W
    Wu, M
    Chin, L
    Mann, KK
    DePinho, RA
    Sonenshein, GE
    [J]. ONCOGENE, 1999, 18 (15) : 2489 - 2498
  • [86] myc boxes, which are conserved in myc family proteins, are signals for protein degradation via the proteasome
    Flinn, EM
    Busch, CMC
    Wright, APH
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (10) : 5961 - 5969
  • [87] Two MAD tails:: what the recent knockouts of Madl and Mxil tell us about the MYC/MAX/MAD network
    Foley, KP
    Eisenman, RN
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 1999, 1423 (03): : M37 - M47
  • [88] Targeted disruption of the MYC antagonist MAD1 inhibits cell cycle exit during granulocyte differentiation
    Foley, KP
    McArthur, GA
    Quéva, C
    Hurlin, PJ
    Soriano, P
    Eisenman, RN
    [J]. EMBO JOURNAL, 1998, 17 (03) : 774 - 785
  • [89] ENFORCED EXPRESSION OF THE C-MYC ONCOGENE INHIBITS CELL-DIFFERENTIATION BY PRECLUDING ENTRY INTO A DISTINCT PREDIFFERENTIATION STATE IN G0/G1
    FREYTAG, SO
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (04) : 1614 - 1624
  • [90] FREYTAG SO, 1990, CELL GROWTH DIFFER, V1, P339