Targeted destruction of DNA replication protein Cdc6 by cell death pathways in mammals and yeast

被引:67
作者
Blanchard, F
Rusiniak, ME
Sharma, K
Sun, XL
Todorov, I
Castellano, MM
Gutierrez, C
Baumann, H [1 ]
Burhans, WC
机构
[1] Roswell Pk Canc Inst, Dept Mol & Cellular Biol, Buffalo, NY 14263 USA
[2] Roswell Pk Canc Inst, Dept Canc Genet, Buffalo, NY 14263 USA
[3] City Hope Natl Med Ctr, Dept Endocrinol & Metab, Duarte, CA 91010 USA
[4] Ctr Biol Mol Severo Ochoa, Consejo Super Invest Cient, Madrid 28049, Spain
[5] Univ Autonoma Madrid, E-28049 Madrid, Spain
关键词
D O I
10.1091/mbc.02-02-0010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The highly conserved Cdc6 protein is required for initiation of eukaryotic DNA replication and, in yeast ad Xenopus, for the coupling of DNA replication to mitosis. Herein, we show that human Cdc6 is rapidly destroyed by a p53-independent, proteasome-, and ubiquitin-dependent pathway during early stages of programmed cell death induced by the DNA-damaging drug adozelesin, or by a separate caspase-dependent pathway in cells undergoing apoptosis through an extrinsic pathway induced by tumor necrosis factor-alpha and cycloheximide. The proteasome-dependent pathway induced by adozelesin is conserved in the budding yeast Saccharomyces cerevisiae. The destruction of Cdc6 may be a primordial programmed death response that uncouples DNA replication from the cell division cycle, which is reinforced in metazoans by the evolution of caspases and p53.
引用
收藏
页码:1536 / 1549
页数:14
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