Id proteins in cell cycle control and cellular senescence

被引:223
作者
Zebedee, Z
Hara, E
机构
[1] Christie Hosp NHS Trust, Paterson Inst Canc Res, CRC Cell Cycle Grp, Manchester M20 4BX, Lancs, England
[2] Univ Manchester, Inst Sci & Technol, Dept Biomol Sci, Manchester M60 1QD, Lancs, England
关键词
Id; cell cycle; senescence; Ets; CDKs; P16(INK4a);
D O I
10.1038/sj.onc.1205092
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 Id family of hefix-loop-helix (HLH) proteins are thought to affect the balance between cell growth and differentiation by negatively regulating the function of basic -helix -loop -helix (bHLH) transcription factors. Although it has been suggested for some time that Id is involved in cell cycle regulation, little is known about the molecular mechanism of this control. Recent studies, however, have revealed that Id binds to important cell cycle regulatory proteins other than bHLH proteins. Two such proteins, pRB (retinoblastoma tumour suppressor protein) family proteins and Ets-family transcription factors are known to play key roles in cell cycle regulation, transformation and tumour suppression. Through the characterization of these pathways we will begin to understand the mechanisms by which Id controls normal and abnormal cell cycle progression.
引用
收藏
页码:8317 / 8325
页数:9
相关论文
共 113 条
  • [81] Reznikoff CA, 1996, CANCER RES, V56, P2886
  • [82] THE EXPRESSION PATTERN OF ID4, A NOVEL DOMINANT-NEGATIVE HELIX-LOOP-HELIX PROTEIN, IS DISTINCT FROM ID1, ID2 AND ID3
    RIECHMANN, V
    VANCRUCHTEN, I
    SABLITZKY, F
    [J]. NUCLEIC ACIDS RESEARCH, 1994, 22 (05) : 749 - 755
  • [83] Id helix-loop-helix proteins antagonize Pax transcription factor activity by inhibiting DNA binding
    Roberts, EC
    Deed, RW
    Inoue, T
    Norton, JD
    Sharrocks, AD
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (02) : 524 - 533
  • [84] Ruas M, 1998, BIOCHIM BIOPHYS ACTA, V1378, P115, DOI 10.1016/s0304-419x(98)00017-1
  • [85] Targeted disruption of the three Rb-related genes leads to loss of G1 control and immortalization
    Sage, J
    Mulligan, GJ
    Attardi, LD
    Miller, A
    Chen, SQ
    Williams, B
    Theodorou, E
    Jacks, T
    [J]. GENES & DEVELOPMENT, 2000, 14 (23) : 3037 - 3050
  • [86] Oncogenic ras provokes premature cell senescence associated with accumulation of p53 and p16(INK4a)
    Serrano, M
    Lin, AW
    McCurrach, ME
    Beach, D
    Lowe, SW
    [J]. CELL, 1997, 88 (05) : 593 - 602
  • [87] A NEW REGULATORY MOTIF IN CELL-CYCLE CONTROL CAUSING SPECIFIC-INHIBITION OF CYCLIN-D/CDK4
    SERRANO, M
    HANNON, GJ
    BEACH, D
    [J]. NATURE, 1993, 366 (6456) : 704 - 707
  • [88] A ROLE FOR BOTH RB AND P53 IN THE REGULATION OF HUMAN CELLULAR SENESCENCE
    SHAY, JW
    PEREIRASMITH, OM
    WRIGHT, WE
    [J]. EXPERIMENTAL CELL RESEARCH, 1991, 196 (01) : 33 - 39
  • [89] Hayflick, his limit, and cellular ageing
    Shay, JW
    Wright, WE
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2000, 1 (01) : 72 - 76
  • [90] SHEN CP, 1995, MOL CELL BIOL, V15, P4518