Hande M P, Lansdorp P M, Natarajan A T
Department of Radiation Genetics and Chemical Mutagenesis, Leiden University, Leiden, Netherlands.
Mutat Res. 1998 Aug 3;404(1-2):205-14. doi: 10.1016/s0027-5107(98)00115-8.
Telomeres serve as protective caps for the chromosome ends. They are one of the functional elements required for the stable transmission of eukaryotic chromosomes. Telomerase, a ribonucleoprotein, stabilises the telomere length by adding telomere repeats on to chromosome ends. Telomeres and telomerase can play a role in the formation of chromosome aberrations and especially in healing of the chromosome or chromatid breaks produced by radiation-induced DNA damage. Telomerase-independent processes also appear to be capable of capping broken chromosome ends. We have studied the expression of telomerase, telomere status and chromosome rearrangements in mouse splenocytes following different doses (0.5, 1.0, 2.0 or 3.0 Gy) of X-irradiation in vivo up to 224 days post-exposure. A dose-dependent increase in telomerase activity up to 2 Gy X-ray exposure was observed immediately after irradiation. The increased enzyme activity was detected even up to day 224 post-irradiation, the last time point studied, especially at higher doses (2 Gy and 3 Gy). A significant difference in average telomere length, measured by quantitative fluorescence in situ hybridisation (Q-FISH) on metaphase chromosomes, noticed immediately after irradiation indicates terminal deletion or altered telomere chromatin. However, telomere length was not statistically significant from the control at the later time points studied. Presence of telomere repeats at the chromosomal breakage sites revealed by FISH with peptide nucleic acid (PNA) telomeric probe indicates a possible role of telomerase-dependent or independent processes in chromosome healing and telomere capture in mammalian cells. We found that approximately 25 to 50% of the newly formed telomeres at the breakage sites are in the range of 200 bp to 1 kb, which might suggest that these repeats could have been added by telomerase which showed a corresponding increase following irradiation.
端粒作为染色体末端的保护帽。它们是真核染色体稳定传递所需的功能元件之一。端粒酶是一种核糖核蛋白,通过在染色体末端添加端粒重复序列来稳定端粒长度。端粒和端粒酶可在染色体畸变的形成中发挥作用,尤其是在修复由辐射诱导的DNA损伤产生的染色体或染色单体断裂方面。不依赖端粒酶的过程似乎也能够封闭断裂的染色体末端。我们研究了在体内不同剂量(0.5、1.0、2.0或3.0 Gy)X射线照射后长达224天的小鼠脾细胞中端粒酶的表达、端粒状态和染色体重排情况。照射后立即观察到,在高达2 Gy X射线照射剂量下,端粒酶活性呈剂量依赖性增加。即使在照射后第224天(研究的最后一个时间点),尤其是在较高剂量(2 Gy和3 Gy)下,仍能检测到酶活性增加。通过中期染色体上的定量荧光原位杂交(Q-FISH)测量的平均端粒长度在照射后立即出现显著差异,这表明存在末端缺失或端粒染色质改变。然而,在所研究的后期时间点,端粒长度与对照组相比无统计学显著差异。用肽核酸(PNA)端粒探针进行荧光原位杂交(FISH)显示,染色体断裂位点存在端粒重复序列,这表明在哺乳动物细胞中,依赖或不依赖端粒酶的过程可能在染色体修复和端粒捕获中发挥作用。我们发现,断裂位点处约25%至50%的新形成端粒长度在200 bp至1 kb范围内,这可能表明这些重复序列可能是由照射后相应增加的端粒酶添加的。