A combinatorial mechanism for determining the specificity of E2F activation and repression

被引:27
作者
Freedman, J. A. [1 ]
Chang, J. T. [1 ]
Jakoi, L. [1 ]
Nevins, J. R. [1 ]
机构
[1] Duke Univ, Med Ctr, Duke Inst Genome Sci & Policy, Durham, NC 27710 USA
关键词
E2F; transcription; gene regulation; TRANSCRIPTION FACTOR; CELL-CYCLE; DNA-REPLICATION; FAMILY-MEMBERS; IN-VIVO; APOPTOSIS; PROLIFERATION; PROMOTER; DISTINCT; BINDING;
D O I
10.1038/onc.2009.153
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
Various studies have detailed the role of E2F proteins in both transcription activation and repression. Further study has shown that distinct promoter elements, but comprising the same E2F-recognition motif, confer positive or negative E2F control and that this reflects binding of either activator or repressor E2F proteins, respectively. We now show that the specificity of binding of an activator or repressor E2F protein is determined by adjacent sequences that bind a cooperating transcription factor. We propose that the functional E2F element is a module comprising not only the E2F-binding site but also the adjacent site for the cooperating transcription factor. Oncogene (2009) 28, 2873-2881; doi:10.1038/onc.2009.153; published online 22 June 2009
引用
收藏
页码:2873 / 2881
页数:9
相关论文
共 54 条
  • [1] Aparicio Oscar, 2005, Curr Protoc Mol Biol, VChapter 21, DOI 10.1002/0471142727.mb2103s69
  • [2] Distinct recruitment of E2F family members to specific E2F-binding sites mediates activation and repression of the E2F1 promoter
    Araki, K
    Nakajima, Y
    Eto, K
    Ikeda, MA
    [J]. ONCOGENE, 2003, 22 (48) : 7632 - 7641
  • [3] p14ARF links the tumour suppressors RB and p53
    Bates, S
    Phillips, AC
    Clark, PA
    Stott, F
    Peters, G
    Ludwig, RL
    Vousden, KH
    [J]. NATURE, 1998, 395 (6698) : 124 - 125
  • [4] JASPAR, the open access database of transcription factor-binding profiles: new content and tools in the 2008 update
    Bryne, Jan Christian
    Valen, Eivind
    Tang, Man-Hung Eric
    Marstrand, Troels
    Winther, Ole
    da Piedade, Isabelle
    Krogh, Anders
    Lenhard, Boris
    Sandelin, Albin
    [J]. NUCLEIC ACIDS RESEARCH, 2008, 36 : D102 - D106
  • [5] Characterization of E2F8, a novel E2F-like cell-cycle regulated repressor of E2F-activated transcription
    Christensen, J
    Cloos, P
    Toftegaard, U
    Klinkenberg, D
    Bracken, AP
    Trinh, E
    Heeran, M
    Di Stefano, L
    Helin, K
    [J]. NUCLEIC ACIDS RESEARCH, 2005, 33 (17) : 5458 - 5470
  • [6] Direct repression of the Mcl-1 promoter by E2F1
    Croxton, R
    Ma, YH
    Song, LX
    Haura, EB
    Cress, WD
    [J]. ONCOGENE, 2002, 21 (09) : 1359 - 1369
  • [7] Identification and characterization of E2F7, a novel mammalian E2F family member capable of blocking cellular proliferation
    de Bruin, A
    Maiti, B
    Jakoi, L
    Timmers, C
    Buerki, R
    Leone, G
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (43) : 42041 - 42049
  • [8] Distinct roles for E2F proteins in cell growth control and apoptosis
    DeGregori, J
    Leone, G
    Miron, A
    Jakoi, L
    Nevins, JR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (14) : 7245 - 7250
  • [9] DeGregori J, 2006, CURR MOL MED, V6, P739
  • [10] E2F7, a novel E2F featuring DP-independent repression of a subset of E2F-regulated genes
    Di Stefano, L
    Jensen, MR
    Helin, K
    [J]. EMBO JOURNAL, 2003, 22 (23) : 6289 - 6298