Chen Yuting, Hu Jiaxin, Zhao Pengwei, Fang Jie, Kuang Yingqi, Liu Zhaojie, Dong Shuling, Yao Weijing, Ding Yuanyuan, Wang Xinhui, Pan Yibin, Wu Jianbin, Zhao Jingwei, Yang Jing, Xu Zhenzhong, Liu Xiaodi, Zhang Yi, Wu Choufei, Zhang Liqin, Fan Mingzhu, Feng Shan, Hong Zhi, Yan Zhangming, Xia Hongguang, Tang Kaiyue, Yang Bing, Liu Wei, Sun Qiming, Mei Kunrong, Zou Wei, Huang Yunpeng, Feng Du, Yi Cong
Department of Biochemistry and Department of Hepatobiliary and Pancreatic Surgery of the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
State Key Laboratory of Respiratory Disease, Guangzhou Municipal and Guangdong Provincial Key Laboratory of Protein Modification and Degradation, School of Basic Medical Sciences, Guangzhou Medical University, Guangzhou, China.
Nat Cell Biol. 2025 Mar;27(3):477-492. doi: 10.1038/s41556-024-01598-2. Epub 2025 Feb 11.
Ribophagy is a selective autophagic process that regulates ribosome turnover. Although NUFIP1 has been identified as a mammalian receptor for ribophagy, its homologues do not exist in yeast and nematodes. Here we demonstrate that Rpl12, a ribosomal large subunit protein, functions as a conserved ribophagy receptor in multiple organisms. Disruption of Rpl12-Atg8s binding leads to significant accumulation of ribosomal proteins and rRNA, while Atg1-mediated Rpl12 phosphorylation enhances its association with Atg11, thus triggering ribophagy during starvation. Ribophagy deficiency accelerates cell death induced by starvation and pathogen infection, leading to impaired growth and development and a shortened lifespan in both Caenorhabditis elegans and Drosophila melanogaster. Moreover, ribophagy deficiency results in motor impairments associated with ageing, while the overexpression of RPL12 significantly improves movement defects induced by starvation, ageing and Aβ accumulation in fly models. Our findings suggest that Rpl12 functions as a conserved ribophagy receptor vital for ribosome metabolism and cellular homeostasis.
核糖体自噬是一种调节核糖体周转的选择性自噬过程。尽管NUFIP1已被鉴定为核糖体自噬的哺乳动物受体,但其同源物在酵母和线虫中并不存在。在这里,我们证明核糖体大亚基蛋白Rpl12在多种生物体中作为保守的核糖体自噬受体发挥作用。Rpl12与Atg8s结合的破坏会导致核糖体蛋白和rRNA的显著积累,而Atg1介导的Rpl12磷酸化增强了其与Atg11的关联,从而在饥饿期间触发核糖体自噬。核糖体自噬缺陷会加速饥饿和病原体感染诱导的细胞死亡,导致秀丽隐杆线虫和黑腹果蝇的生长发育受损和寿命缩短。此外,核糖体自噬缺陷会导致与衰老相关的运动障碍,而RPL12的过表达显著改善了果蝇模型中由饥饿、衰老和Aβ积累引起的运动缺陷。我们的研究结果表明,Rpl12作为一种保守的核糖体自噬受体,对核糖体代谢和细胞稳态至关重要。