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Arabidopsis ATM and ATR Kinases Prevent Propagation of Genome Damage Caused by Telomere Dysfunction

机译:拟南芥ATM和ATR激酶可防止端粒功能障碍引起的基因组损伤的传播

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摘要

The ends of linear eukaryotic chromosomes are hidden in nucleoprotein structures called telomeres, and loss of the telomere structure causes inappropriate repair, leading to severe karyotypic and genomic instability. Although it has been shown that DNA damaging agents activate a DNA damage response (DDR), little is known about the signaling of dysfunctional plant telomeres. We show that absence of telomerase in Arabidopsis thaliana elicits an ATAXIA-TELANGIECTASIA MUTATED (ATM) and ATM AND RAD3-RELATED (ATR)-dependent DDR at telomeres, principally through ATM. By contrast, telomere dysfunction induces an ATR-dependent response in telomeric Conserved telomere maintenance component1 (Ctc1)-Suppressor of cdc thirteen (Stn1)-Telomeric pathways in association with Stn1 (CST)–complex mutants. These results uncover a new role for the CST complex in repressing the ATR-dependent DDR pathway in plant cells and show that plant cells use two different DNA damage surveillance pathways to signal telomere dysfunction. The absence of either ATM or ATR in ctc1 and stn1 mutants significantly enhances developmental and genome instability while reducing stem cell death. These data thus give a clear illustration of the action of ATM/ATR-dependent programmed cell death in maintaining genomic integrity through elimination of genetically unstable cells.
机译:线性真核染色体的末端隐藏在称为端粒的核蛋白结构中,端粒结构的缺失会导致不适当的修复,从而导致严重的核型和基因组不稳定。尽管已经显示出DNA破坏剂会激活DNA损伤反应(DDR),但对于功能失调的植物端粒的信号知之甚少。我们显示,在拟南芥中没有端粒酶会引起ATAXIA-TELANGIECTASIA MUTATED(ATM)和ATM和RAD3相关(ATR)依赖的DDR在端粒,主要是通过ATM。相比之下,端粒功能障碍在端粒保守端粒维持组分1(Ctc1)-cdc十三(Stn1)-端粒途径的抑制子与Stn1(CST)-复杂突变体相关联时诱导ATR依赖性反应。这些结果揭示了CST复合体在抑制植物细胞中ATR依赖的DDR途径中的新作用,并表明植物细胞使用两种不同的DNA损伤监测途径来信号端粒功能障碍。 ctc1和stn1突变体中不存在ATM或ATR,可显着增强发育和基因组的不稳定性,同时减少干细胞死亡。因此,这些数据清楚地说明了依赖ATM / ATR的程序性细胞死亡在通过消除遗传上不稳定的细胞来维持基因组完整性方面的作用。

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