Department of Genome Dynamics, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague 4, 142 20, Czech Republic.
Genome Damage and Stability Centre, University of Sussex, Falmer, Brighton BN1 9RQ, UK.
Nucleic Acids Res. 2020 Jul 9;48(12):6672-6684. doi: 10.1093/nar/gkaa489.
Hereditary mutations in polynucleotide kinase-phosphatase (PNKP) result in a spectrum of neurological pathologies ranging from neurodevelopmental dysfunction in microcephaly with early onset seizures (MCSZ) to neurodegeneration in ataxia oculomotor apraxia-4 (AOA4) and Charcot-Marie-Tooth disease (CMT2B2). Consistent with this, PNKP is implicated in the repair of both DNA single-strand breaks (SSBs) and DNA double-strand breaks (DSBs); lesions that can trigger neurodegeneration and neurodevelopmental dysfunction, respectively. Surprisingly, however, we did not detect a significant defect in DSB repair (DSBR) in primary fibroblasts from PNKP patients spanning the spectrum of PNKP-mutated pathologies. In contrast, the rate of SSB repair (SSBR) is markedly reduced. Moreover, we show that the restoration of SSBR in patient fibroblasts collectively requires both the DNA kinase and DNA phosphatase activities of PNKP, and the fork-head associated (FHA) domain that interacts with the SSBR protein, XRCC1. Notably, however, the two enzymatic activities of PNKP appear to affect different aspects of disease pathology, with reduced DNA phosphatase activity correlating with neurodevelopmental dysfunction and reduced DNA kinase activity correlating with neurodegeneration. In summary, these data implicate reduced rates of SSBR, not DSBR, as the source of both neurodevelopmental and neurodegenerative pathology in PNKP-mutated disease, and the extent and nature of this reduction as the primary determinant of disease severity.
多核苷酸激酶-磷酸酶(PNKP)中的遗传突变导致一系列神经病理学改变,范围从伴有早发性癫痫的小头畸形(MCSZ)的神经发育功能障碍到共济失调眼动失用症-4(AOA4)和遗传性运动感觉神经病 2B 型(CMT2B2)的神经退行性变。与此一致,PNKP 参与 DNA 单链断裂(SSB)和 DNA 双链断裂(DSB)的修复;这些损伤分别可以引发神经退行性变和神经发育功能障碍。然而,令人惊讶的是,我们没有在跨越 PNKP 突变病理学谱的 PNKP 患者的原代成纤维细胞中检测到 DSB 修复(DSBR)的显著缺陷。相比之下,SSB 修复(SSBR)的速率明显降低。此外,我们表明,在患者成纤维细胞中,SSBR 的恢复共同需要 PNKP 的 DNA 激酶和 DNA 磷酸酶活性,以及与 SSBR 蛋白 XRCC1 相互作用的叉头相关(FHA)结构域。值得注意的是,然而,PNKP 的两种酶活性似乎影响疾病病理学的不同方面,降低的 DNA 磷酸酶活性与神经发育功能障碍相关,而降低的 DNA 激酶活性与神经退行性变相关。总之,这些数据表明,SSBR 而非 DSBR 的降低率是 PNKP 突变疾病中神经发育和神经退行性病变的根源,而这种降低的程度和性质是疾病严重程度的主要决定因素。