Zhou Jiale, Han Yang, Ji Fuxi, Zhang Renquan, Liang Yuru, Zhao Xudong, Hou Ruizhe
Department of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun, China.
Key Laboratory of Zoonosis Research, Ministry of Education, College of Veterinary Medicine, Jilin University, Changchun, China.
Front Genet. 2025 Apr 16;16:1477542. doi: 10.3389/fgene.2025.1477542. eCollection 2025.
NSUN2 and NSUN6, two family members of NOL1/NSUN protein, are mainly responsible for catalyzing the formation of 5-methylcytosine (m5C) in RNA and highly involved in the physiological and pathological processes of many diseases. To investigate the biological functions of NSUN2 and NSUN6, NSUN2 and NSUN6 HEK293T cell lines were separately constructed by CRISPR/Cas9. We found no significant interaction between the protein expression of NSUN2 and NSUN6. Notably, the ablation of NSUN2 or NSUN6 reduced cell proliferation and increased expression of the senescence-associated marker P27, whereas more β-galactosidase-positive cells were observed in response to HO-induced oxidative stress. Moreover, the expression of NSUN2 and NSUN6 was significantly reduced in the HGPS premature aging cell lines by the LMNA mutation. Taken together, we demonstrated that NSUN2 and NSUN6 may be inextricably linked to cellular aging and thus provide potential novel strategies for the clinical therapeutics of aging and age-associated disease in the future.
NOL1/NSUN蛋白家族的两个成员NSUN2和NSUN6主要负责催化RNA中5-甲基胞嘧啶(m5C)的形成,并高度参与多种疾病的生理和病理过程。为了研究NSUN2和NSUN6的生物学功能,通过CRISPR/Cas9分别构建了NSUN2和NSUN6的HEK293T细胞系。我们发现NSUN2和NSUN6的蛋白表达之间没有显著的相互作用。值得注意的是,敲除NSUN2或NSUN6会降低细胞增殖并增加衰老相关标志物P27的表达,而在HO诱导的氧化应激反应中观察到更多β-半乳糖苷酶阳性细胞。此外,在因LMNA突变导致的HGPS早衰细胞系中,NSUN2和NSUN6的表达显著降低。综上所述,我们证明NSUN2和NSUN6可能与细胞衰老有着千丝万缕的联系,从而为未来衰老及衰老相关疾病的临床治疗提供潜在的新策略。