pRB contains an E2F1-specific binding domain that allows E2F1-induced apoptosis to be regulated separately from other E2Factivities

被引:111
作者
Dick, FA [1 ]
Dyson, N [1 ]
机构
[1] Massachusetts Gen Hosp, Ctr Canc, Charlestown, MA 02129 USA
关键词
D O I
10.1016/S1097-2765(03)00344-7
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
The interaction between pRB and E2F is critical for control of the cell cycle and apoptosis. Here we report that pRB contains two distinct E2F binding sites. The previously identified E2F binding site on pRB is necessary for stable association with E2Fs on DNA. A second E2F interaction site is located entirely within the C-terminal domain of pRB and is specific for E2F1. E2F1/pRB complexes formed through this site have low affinity for DNA, but the interaction is sufficient for pRB to regulate E2F1-induced apoptosis, and E2F1 loses the ability to interact with this site following DNA damage. These results show that pRB interacts with individual E2F proteins in different ways and suggest that pRB's regulation of E2F1-induced apoptosis is physically separable from its transcriptional control of other E2F proteins.
引用
收藏
页码:639 / 649
页数:11
相关论文
共 62 条
  • [1] ADENOVIRUS-E1A PREVENTS THE RETINOBLASTOMA GENE-PRODUCT FROM COMPLEXING WITH A CELLULAR TRANSCRIPTION FACTOR
    BANDARA, LR
    LATHANGUE, NB
    [J]. NATURE, 1991, 351 (6326) : 494 - 497
  • [2] Blattner C, 1999, MOL CELL BIOL, V19, P3704
  • [3] Retinoblastoma protein recruits histone deacetylase to repress transcription
    Brehm, A
    Miska, EA
    McCance, DJ
    Reid, JL
    Bannister, AJ
    Kouzarides, T
    [J]. NATURE, 1998, 391 (6667) : 597 - 601
  • [4] Inhibition of cyclin-dependent kinase 2 by p21 is necessary for retinoblastoma protein-mediated G1 arrest after γ-irradiation
    Brugarolas, J
    Moberg, K
    Boyd, SD
    Taya, Y
    Jacks, T
    Lees, JA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (03) : 1002 - 1007
  • [5] G1 cyclin/cyclin-dependent kinase-coordinated phosphorylation of endogenous pocket proteins differentially regulates their interactions with E2F4 and E2F1 and gene expression
    Calbó, J
    Parreño, M
    Sotillo, E
    Yong, T
    Mazo, A
    Garriga, J
    Graña, X
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (52) : 50263 - 50274
  • [6] THE E2F TRANSCRIPTION FACTOR IS A CELLULAR TARGET FOR THE RB PROTEIN
    CHELLAPPAN, SP
    HIEBERT, S
    MUDRYJ, M
    HOROWITZ, JM
    NEVINS, JR
    [J]. CELL, 1991, 65 (06) : 1053 - 1061
  • [7] Mutant mouse models reveal the relative roles of E2F1 and E2F3 in vivo
    Cloud, JE
    Rogers, C
    Reza, TL
    Ziebold, U
    Stone, JR
    Picard, MH
    Caron, AM
    Bronson, RT
    Lees, JA
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (08) : 2663 - 2672
  • [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] E2F-1 ACCUMULATION BYPASSES A G(1) ARREST RESULTING FROM THE INHIBITION OF G(1) CYCLIN-DEPENDENT KINASE-ACTIVITY
    DEGREGORI, J
    LEONE, G
    OHTANI, K
    MIRON, A
    NEVINS, JR
    [J]. GENES & DEVELOPMENT, 1995, 9 (23) : 2873 - 2887
  • [10] Mutagenesis of the pRB pocket reveals that cell cycle arrest functions are separable from binding to viral oncoproteins
    Dick, FA
    Sailhamer, E
    Dyson, NJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (10) : 3715 - 3727