CUL-4 ubiquitin ligase maintains genome stability by restraining DNA-replication licensing

被引:259
作者
Zhong, WW [1 ]
Feng, H [1 ]
Santiago, FE [1 ]
Kipreos, ET [1 ]
机构
[1] Univ Georgia, Dept Cellular Biol, Athens, GA 30602 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature01747
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To maintain genome stability, DNA replication is strictly regulated to occur only once per cell cycle. In eukaryotes, the presence of 'licensing proteins' at replication origins during the G1 cell-cycle phase allows the formation of the pre-replicative complex(1). The removal of licensing proteins from chromatin during the S phase ensures that origins fire only once per cell cycle(1). Here we show that the CUL-4 ubiquitin ligase temporally restricts DNA-replication licensing in Caenorhabditis elegans. Inactivation of CUL-4 causes massive DNA re-replication, producing cells with up to 100C DNA content. The C. elegans orthologue of the replication-licensing factor Cdt1 (refs 2, 3) is required for DNA replication. C. elegans CDT-1 is present in G1-phase nuclei but disappears as cells enter S phase. In cells lacking CUL-4, CDT-1 levels fail to decrease during S phase and instead remain constant in the re-replicating cells. Removal of one genomic copy of cdt-1 suppresses the cul-4 re-replication phenotype. We propose that CUL-4 prevents aberrant re-initiation of DNA replication, at least in part, by facilitating the degradation of CDT-1.
引用
收藏
页码:885 / 889
页数:6
相关论文
共 30 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   Replication licensing - defining the proliferative state? [J].
Blow, JJ ;
Hodgson, B .
TRENDS IN CELL BIOLOGY, 2002, 12 (02) :72-78
[3]   The control of mammalian DNA replication: A brief history of space and timing [J].
Cimbora, DM ;
Groudine, M .
CELL, 2001, 104 (05) :643-646
[4]   Endoreplication cell cycles: More for less [J].
Edgar, BA ;
Orr-Weaver, TL .
CELL, 2001, 105 (03) :297-306
[5]   DNA-SYNTHESIS AND THE CONTROL OF EMBRYONIC GENE-EXPRESSION IN C-ELEGANS [J].
EDGAR, LG ;
MCGHEE, JD .
CELL, 1988, 53 (04) :589-599
[6]   CUL-2 is required for the G1-to-S-phase transition and mitotic chromosome condensation in Caenorhabditis elegans [J].
Feng, H ;
Zhong, WW ;
Punkosdy, G ;
Gu, SB ;
Zhou, L ;
Seabolt, EK ;
Kipreos, ET .
NATURE CELL BIOLOGY, 1999, 1 (08) :486-492
[7]   Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans [J].
Fire, A ;
Xu, SQ ;
Montgomery, MK ;
Kostas, SA ;
Driver, SE ;
Mello, CC .
NATURE, 1998, 391 (6669) :806-811
[8]   POLYPLOID TISSUES IN THE NEMATODE CAENORHABDITIS-ELEGANS [J].
HEDGECOCK, EM ;
WHITE, JG .
DEVELOPMENTAL BIOLOGY, 1985, 107 (01) :128-133
[9]   THE UNC-5, UNC-6, AND UNC-40 GENES GUIDE CIRCUMFERENTIAL MIGRATIONS OF PIONEER AXONS AND MESODERMAL CELLS ON THE EPIDERMIS IN C-ELEGANS [J].
HEDGECOCK, EM ;
CULOTTI, JG ;
HALL, DH .
NEURON, 1990, 4 (01) :61-85
[10]   Mitosis-specific phosphorylation of histone H3 initiates primarily within pericentromeric heterochromatin during G2 and spreads in an ordered fashion coincident with mitotic chromosome condensation [J].
Hendzel, MJ ;
Wei, Y ;
Mancini, MA ;
VanHooser, A ;
Ranalli, T ;
Brinkley, BR ;
BazettJones, DP ;
Allis, CD .
CHROMOSOMA, 1997, 106 (06) :348-360