How Telomeres Solve the End-Protection Problem

被引:619
作者
de Lange, Titia [1 ]
机构
[1] Rockefeller Univ, Lab Cell Biol & Genet, New York, NY 10021 USA
关键词
DNA-DAMAGE CHECKPOINT; BINDING-PROTEIN; FISSION YEAST; CELL-CYCLE; HOMOLOGOUS RECOMBINATION; SACCHAROMYCES-CEREVISIAE; DYSFUNCTIONAL TELOMERES; UNPROTECTED TELOMERES; MAMMALIAN TELOMERES; POT1; PROTEINS;
D O I
10.1126/science.1170633
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
The ends of eukaryotic chromosomes have the potential to be mistaken for damaged or broken DNA and must therefore be protected from cellular DNA damage response pathways. Otherwise, cells might permanently arrest in the cell cycle, and attempts to "repair" the chromosome ends would have devastating consequences for genome integrity. This end-protection problem is solved by protein-DNA complexes called telomeres. Studies of mammalian cells have recently uncovered the mechanism by which telomeres disguise the chromosome ends. Comparison to unicellular eukaryotes reveals key differences in the DNA damage response systems that inadvertently threaten chromosome ends. Telomeres appear to be tailored to these variations, explaining their variable structure and composition.
引用
收藏
页码:948 / 952
页数:5
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