Wei Chao, Skopp Rose, Takata Minoru, Takeda Shunichi, Price Carolyn M
Department of Molecular Genetics, Biochemistry and Microbiology, College of Medicine, University of Cincinnati, ML0524, 231 Albert Sabin Way, Cincinnati, OH 45267, USA.
Nucleic Acids Res. 2002 Jul 1;30(13):2862-70. doi: 10.1093/nar/gkf396.
Although telomeres are not recognized as double-strand breaks (DSBs), some DSB repair proteins are present at telomeres and are required for telomere maintenance. To learn more about the telomeric function of proteins from the homologous recombination (HR) and non-homologous end joining pathways (NHEJ), we have screened a panel of chicken DT40 knockout cell lines for changes in telomere structure. In contrast to what has been observed in Ku-deficient mice, we found that Ku70 disruption did not result in telomere-telomere fusions and had no effect on telomere length or the structure of the telomeric G-strand overhang. G-overhang length was increased by Rad51 disruption but unchanged by disruption of DNA-PKcs, Mre11, Rad52, Rad54, XRCC2 or XRCC3. The effect of Rad51 depletion was unexpected because gross alterations in telomere structure have not been detected in yeast HR mutants. Thus, our results indicate that Rad51 has a previously undiscovered function at vertebrate telomeres. They also indicate that Mre11 is not required to generate G-overhangs. Although Mre11 has been implicated in overhang generation, overhang structure had not previously been examined in Mre11-deficient cells. Overall our findings indicate that there are significant species-specific differences in the telomeric function of DSB repair proteins.
尽管端粒不被视为双链断裂(DSB),但一些DSB修复蛋白存在于端粒中,是端粒维持所必需的。为了更多地了解同源重组(HR)和非同源末端连接途径(NHEJ)中蛋白质的端粒功能,我们筛选了一组鸡DT40基因敲除细胞系,以观察端粒结构的变化。与在Ku缺陷小鼠中观察到的情况相反,我们发现Ku70的破坏不会导致端粒-端粒融合,对端粒长度或端粒G链悬突的结构也没有影响。Rad51的破坏会增加G悬突长度,而DNA-PKcs、Mre11、Rad52、Rad54、XRCC2或XRCC3的破坏则不会改变G悬突长度。Rad51缺失的影响出乎意料,因为在酵母HR突变体中未检测到端粒结构的明显改变。因此,我们的结果表明Rad51在脊椎动物端粒中具有以前未被发现的功能。它们还表明产生G悬突不需要Mre11。尽管Mre11与悬突的产生有关,但以前尚未在Mre11缺陷细胞中研究过悬突结构。总体而言,我们的发现表明DSB修复蛋白的端粒功能存在显著的物种特异性差异。