Long Jing, Zhao Jian, Chen Jingmin, Ding Jianing, Liu Xiao, Li Zhe, Bian Po, Wang Ting, Jin Wenjie, Lu Xihong, Zhang Yifan, Zhou Libin, Du Yan
Biophysics Group, Biomedical Center, Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
DNA Res. 2025 Jul 4;32(4). doi: 10.1093/dnares/dsaf014.
DNA double-strand breaks (DSBs) repair via POLQ-mediated alternative end-joining (Alt-EJ) is error-prone and mutagenic. However, Alt-EJ is often inhibited by classical nonhomologous end-joining (C-NHEJ) or homologous recombination, the precise impact of Alt-EJ on plant genome instability remains unclear. Here, we employed carbon-ion beam (CIB) which induce complex DSBs to bias cellular repair strategies toward Alt-EJ; additionally, a specific genetic background of C-NHEJ deficiency (lig4-4) Arabidopsis thaliana line and the POLQ-deficient (teb-3 and teb-8) were combined to further amplify the mutagenic effects of CIB mediated by Alt-EJ. The lig4-4 exhibited higher sensitivity to CIB than POLQ-deficient lines. teb-8 exhibited constitutive DNA damage response (DDR), whereas DDR in lig4-4 was strictly induced by CIB. At genome scale, lig4-4 showed substantial changes in the insertion and deletion (InDels) mutation profile, with a higher proportion and larger size of InDels as well as greater microhomology dependence than wild-type. In contrast, teb-8 showed moderate changes, including increased single-base InDels and complex mutations, but lacking > 30 bp InDels. Loss-of-function in LIG4 and POLQ resulted in a higher proportion of high-impact genome mutations than wild-type even at lower doses. These findings offered essential insights for the development of a novel repair pathway-driven heavy-ion beam mutagenesis system.
通过POLQ介导的替代性末端连接(Alt-EJ)进行的DNA双链断裂(DSB)修复容易出错且具有致突变性。然而,Alt-EJ通常会受到经典非同源末端连接(C-NHEJ)或同源重组的抑制,Alt-EJ对植物基因组不稳定性的确切影响仍不清楚。在这里,我们采用碳离子束(CIB)来诱导复杂的DSB,使细胞修复策略偏向于Alt-EJ;此外,将C-NHEJ缺陷(lig4-4)拟南芥品系的特定遗传背景与POLQ缺陷(teb-3和teb-8)相结合,以进一步放大由Alt-EJ介导的CIB的诱变效应。lig4-4对CIB的敏感性高于POLQ缺陷品系。teb-8表现出组成型DNA损伤反应(DDR),而lig4-4中的DDR则严格由CIB诱导。在基因组规模上,lig4-4在插入和缺失(InDels)突变谱上显示出实质性变化,与野生型相比,InDels的比例更高、大小更大,并且对微同源性的依赖性更强。相比之下,teb-8表现出适度的变化,包括单碱基InDels增加和复杂突变,但缺乏>30 bp的InDels。即使在较低剂量下,LIG4和POLQ的功能丧失也导致比野生型更高比例的高影响基因组突变。这些发现为开发一种新型的由修复途径驱动的重离子束诱变系统提供了重要见解。