Ihara Dai, Narumoto Ayano, Kande Yukie, Hayashi Tomoki, Ikuno Yasuaki, Shirai Manabu, Wakabayashi Masaki, Nitta Ryo, Naka-Kaneda Hayato, Katsuyama Yu
Department of Anatomy, Shiga University of Medical Science, Shiga, Japan.
Omics Research Center, National Cerebral and Cardiovascular Center, Osaka, Japan.
Cell Death Discov. 2025 Jul 24;11(1):342. doi: 10.1038/s41420-025-02640-4.
Neurons are subjected to various stresses, including high metabolic demand, physiological activity, and transcriptional regulation, to which their genomic DNA are vulnerable. Genome stability of neurons is essential for proper physiological brain function. Failure in accurate genomic DNA repair can result in abnormal neuronal functions or cell death. Genomic instability has been implicated in increased risks of neurodevelopmental and neurodegenerative disorders. However, the molecular mechanisms underlying neuronal genome stability remain poorly understood. Mutations in the Strawberry Notch Homolog 1 (SBNO1) have been suggested to contribute to these disorders. Here, we investigated the molecular mechanisms underlying histological abnormalities observed in the cortex of Sbno1 knockout (KO) mice. Comprehensive gene expression analysis revealed that Sbno1 KO affects the expression of genes related to cell survival, consistent with the increased apoptosis observed in Sbno1 KO cortices. Among the genes downregulated in Sbno1 KO, we focused on Yeats4. Overexpression of Yeats4 rescued the accumulation of genomic DNA damage and cell death caused by Sbno1 deletion. These findings suggest that Sbno1 is critical in safeguarding the neuronal genome, at least in part, via regulating Yeats4 expression.
神经元会受到各种应激,包括高代谢需求、生理活动和转录调控,而它们的基因组DNA对此很脆弱。神经元的基因组稳定性对于正常的生理性脑功能至关重要。准确的基因组DNA修复失败会导致神经元功能异常或细胞死亡。基因组不稳定与神经发育和神经退行性疾病风险增加有关。然而,神经元基因组稳定性背后的分子机制仍知之甚少。草莓Notch同源物1(SBNO1)的突变被认为与这些疾病有关。在此,我们研究了在Sbno1基因敲除(KO)小鼠皮质中观察到的组织学异常背后的分子机制。综合基因表达分析表明,Sbno1基因敲除会影响与细胞存活相关基因的表达,这与在Sbno1基因敲除皮质中观察到的细胞凋亡增加一致。在Sbno1基因敲除中下调的基因中,我们重点关注了Yeats4。Yeats4的过表达挽救了由Sbno1缺失导致的基因组DNA损伤积累和细胞死亡。这些发现表明,Sbno1至少部分通过调节Yeats4的表达在保护神经元基因组方面至关重要。