Brunori Michele, Gilson Eric
Laboratoire de Biologie Moléculaire de la Cellule, UMR5161, Centre National de la Recherche Scientifique, Ecole Normale Supérieure de Lyon, INRA U1237, 46, allée d'Italie, 69364 Lyon cedex 07, France.
J Soc Biol. 2004;198(2):105-11.
Telomeres are nucleoprotein complexes that cap the end of eukaryotic chromosomes. They are essential for the functions and the stability of the genomes. In the absence of telomerase, the enzyme that adds telomeric DNA repeats to chromosome ends, telomeres shorten with cell division, a process thought to contribute to cell senescence. Reciprocally, telomere stabilization in immortalized cells, that usually appears concomitant with detection of telomerase activity, suggests that telomerase is essential for unlimited cell proliferation. Sequential modifications in the function of telomeres play antagonistic functions as far as tumorigenesis is concerned. Telomere dysfunction is thought to promote genome instability at initial stages, favoring the emergence of cancer-associated chromosomal abnormalities; reestablishment of telomere maintenance is expected afterwards if efficient cell cycling is to occur.
端粒是覆盖真核染色体末端的核蛋白复合体。它们对于基因组的功能和稳定性至关重要。在缺乏端粒酶(一种向染色体末端添加端粒DNA重复序列的酶)的情况下,端粒会随着细胞分裂而缩短,这一过程被认为与细胞衰老有关。相反,永生化细胞中的端粒稳定,通常与端粒酶活性的检测同时出现,这表明端粒酶对于细胞的无限增殖至关重要。就肿瘤发生而言,端粒功能的一系列改变发挥着拮抗作用。端粒功能障碍被认为在初始阶段会促进基因组不稳定,有利于出现与癌症相关的染色体异常;如果要实现有效的细胞周期循环,随后预计会重新建立端粒维持机制。