Heacock Michelle L, Idol Rachel A, Friesner Joanna D, Britt Anne B, Shippen Dorothy E
Department of Biochemistry and Biophysics, Texas A&M University 2128 TAMU, College Station, TX 77843-2128, USA.
Nucleic Acids Res. 2007;35(19):6490-500. doi: 10.1093/nar/gkm472. Epub 2007 Sep 25.
In the absence of the telomerase, telomeres undergo progressive shortening and are ultimately recruited into end-to-end chromosome fusions via the non-homologous end joining (NHEJ) double-strand break repair pathway. Previously, we showed that fusion of critically shortened telomeres in Arabidopsis proceeds with approximately the same efficiency in the presence or absence of KU70, a key component of NHEJ. Here we report that DNA ligase IV (LIG4) is also not essential for telomere joining. We observed only a modest decrease (3-fold) in the frequency of chromosome fusions in triple tert ku70 lig4 mutants versus tert ku70 or tert. Sequence analysis revealed that, relative to tert ku70, chromosome fusion junctions in tert ku70 lig4 mutants contained less microhomology and less telomeric DNA. These findings argue that the KU-LIG4 independent end-joining pathway is less efficient and mechanistically distinct from KU-independent NHEJ. Strikingly, in all the genetic backgrounds we tested, chromosome fusions are initiated when the shortest telomere in the population reaches approximately 1 kb, implying that this size represents a critical threshold that heralds a detrimental structural transition. These data reveal the transitory nature of telomere stability, and the robust and flexible nature of DNA repair mechanisms elicited by telomere dysfunction.
在没有端粒酶的情况下,端粒会逐渐缩短,并最终通过非同源末端连接(NHEJ)双链断裂修复途径被招募到端对端的染色体融合中。此前,我们发现,在拟南芥中,无论有无NHEJ的关键组分KU70,严重缩短的端粒的融合效率大致相同。在此我们报告,DNA连接酶IV(LIG4)对于端粒连接也不是必需的。我们观察到,与tert ku70或tert相比,三重突变体tert ku70 lig4中染色体融合频率仅适度降低(3倍)。序列分析显示,相对于tert ku70,tert ku70 lig4突变体中的染色体融合连接处含有更少的微同源性和更少的端粒DNA。这些发现表明,KU-LIG4非依赖性末端连接途径效率较低,且在机制上与KU非依赖性NHEJ不同。引人注目的是,在我们测试的所有遗传背景中,当群体中最短的端粒达到约1 kb时,染色体融合就会开始,这意味着这个长度代表了一个关键阈值,预示着有害的结构转变。这些数据揭示了端粒稳定性的短暂性,以及端粒功能障碍引发的DNA修复机制的稳健性和灵活性。