cul-1 is required for cell cycle exit in C-elegans and identifies a novel gene family

被引:392
|
作者
Kipreos, ET
Lander, LE
Wing, JP
He, WW
Hedgecock, EM
机构
[1] JOHNS HOPKINS UNIV, DEPT BIOL, BALTIMORE, MD 21218 USA
[2] HUMAN GENOME SCI INC, ROCKVILLE, MD 20850 USA
关键词
D O I
10.1016/S0092-8674(00)81267-2
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 gene cul-1 (formerly lin-19) is a negative regulator of the cell cycle in C. elegans. Null mutations cause hyperplasia of all tissues. cul-1 is required for developmentally programmed transitions from the G1 phase of the cell cycle to the G0 phase or the apoptotic pathway. Moreover, the mutant phenotype suggests that G1-to-S phase progression is accelerated, overriding mechanisms for mitotic arrest and producing abnormally small cells. Significantly, diverse aspects of cell fate and differentiation are unaffected in cul-1 mutants. cul-1 represents a conserved family of genes, designated cullins, with at least five members in nematodes, six in humans, and three in budding yeast.
引用
收藏
页码:829 / 839
页数:11
相关论文
共 50 条
  • [41] A polycystic kidney-disease gene homologue required for male mating behaviour in C-elegans
    Barr, MM
    Sternberg, PW
    NATURE, 1999, 401 (6751) : 386 - 389
  • [42] POP-1 is required for asymmetric cell fates mediated by Wnt/Wingless signaling in C-elegans embryogenesis
    Lin, RL
    Priess, JR
    DEVELOPMENTAL BIOLOGY, 1997, 186 (02) : S31 - S31
  • [43] eor-1 and eor-2 are required for cell-specific apoptotic death in C-elegans
    Hoeppner, DJ
    Spector, MS
    Ratliff, TM
    Kinchen, JM
    Granat, S
    Lin, SC
    Bhusri, SS
    Conradt, B
    Herman, MA
    Hengartner, MO
    DEVELOPMENTAL BIOLOGY, 2004, 274 (01) : 125 - 138
  • [44] SKN-1, A MATERNALLY EXPRESSED GENE REQUIRED TO SPECIFY THE FATE OF VENTRAL BLASTOMERES IN THE EARLY C-ELEGANS EMBRYO
    BOWERMAN, B
    EATON, BA
    PRIESS, JR
    CELL, 1992, 68 (06) : 1061 - 1075
  • [45] The C-elegans lissencephaly disease gene homolog lis-1 is required for embryonic development, axonal pathfinding, and neurotransmission
    Buttner, EA
    Horvitz, HR
    NEUROLOGY, 2002, 58 (07) : A10 - A11
  • [46] Neuronal cell migration in C-elegans: Regulation of Hox gene expression and cell position
    Harris, J
    Honigberg, L
    Robinson, N
    Kenyon, C
    DEVELOPMENT, 1996, 122 (10): : 3117 - 3131
  • [47] Ebf gene function is required for coupling neuronal differentiation and cell cycle exit
    Garcia-Dominguez, M
    Poquet, C
    Garel, S
    Charnay, P
    DEVELOPMENT, 2003, 130 (24): : 6013 - 6025
  • [48] The C-elegans Myt1 ortholog is required for the proper timing of oocyte maturation
    Burrows, AE
    Sceurman, BK
    Kosinski, ME
    Richie, CT
    Sadler, PL
    Schumacher, JM
    Golden, A
    DEVELOPMENT, 2006, 133 (04): : 697 - 709
  • [49] SAS-6 defines a protein family required for centrosome duplication in C-elegans and in human cells
    Leidel, S
    Delattre, M
    Cerutti, L
    Baumer, K
    Gönczy, P
    NATURE CELL BIOLOGY, 2005, 7 (02) : 115 - U19
  • [50] Fluoxetine-resistant mutants in C-elegans define a novel family of transmembrane proteins
    Choy, RKM
    Thomas, JH
    MOLECULAR CELL, 1999, 4 (02) : 143 - 152