Long G tails at both ends of human chromosomes suggest a C strand degradation mechanism for telomere shortening

被引:744
作者
Makarov, VL [1 ]
Hirose, Y [1 ]
Langmore, JP [1 ]
机构
[1] UNIV MICHIGAN,DEPT BIOL SCI,ANN ARBOR,MI 48109
基金
美国国家科学基金会;
关键词
D O I
10.1016/S0092-8674(00)81908-X
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 chromosomes of lower eukaryotes have short telomeric 3' extensions. Using a primer-extension/nick-translation technique and nondenaturing hybridization, we find long 3' G-rich tails at human chromosome ends in mortal primary fibroblasts, umbilical vein endothelial cells, and leukocytes, as well as in immortalized fibroblasts. For all cells tested, >80% of the telomeres have long G-rich overhangs, averaging 130-210 bases in length, in disagreement with the conventional model for incomplete lagging-strand replication, which predicts overhangs on 50% of the chromosome ends. The observed G tails must exist during most of the cell cycle and probably result from degradation of both chromosome ends. The average lengths of the G tails are quantitatively consistent with the observed rates of human chromosome shortening.
引用
收藏
页码:657 / 666
页数:10
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