Liu Yanyan, Li Mengmeng, Lin Miao, Liu Xinjie, Guo Haolin, Tan Junyang, Hu Liubing, Li Jianshuang, Zhou Qinghua
Key Laboratory of Regenerative Medicine of Ministry of Education, The First Affiliated Hospital, Jinan University, Guangzhou, 510632, Guangdong, China.
The College of Life Science and Technology, Jinan University, Guangzhou, 510632, Guangdong, China.
Cell Mol Life Sci. 2024 Mar 12;81(1):130. doi: 10.1007/s00018-024-05152-z.
ALKBH1 is a typical demethylase of nucleic acids, which is correlated with multiple types of biological processes and human diseases. Recent studies are focused on the demethylation of ALKBH1, but little is known about its non-demethylase function. Here, we demonstrate that ALKBH1 regulates the glycolysis process through HIF-1α signaling in a demethylase-independent manner. We observed that depletion of ALKBH1 inhibits glycolysis flux and extracellular acidification, which is attributable to reduced HIF-1α protein levels, and it can be rescued by reintroducing HIF-1α. Mechanistically, ALKBH1 knockdown enhances chaperone-mediated autophagy (CMA)-mediated HIF-1α degradation by facilitating the interaction between HIF-1α and LAMP2A. Furthermore, we identify that ALKBH1 competitively binds to the OST48, resulting in compromised structural integrity of oligosaccharyltransferase (OST) complex and subsequent defective N-glycosylation of LAMPs, particularly LAMP2A. Abnormal glycosylation of LAMP2A disrupts lysosomal homeostasis and hinders the efficient degradation of HIF-1α through CMA. Moreover, NGI-1, a small-molecule inhibitor that selectively targets the OST complex, could inhibit the glycosylation of LAMPs caused by ALKBH1 silencing, leading to impaired CMA activity and disruption of lysosomal homeostasis. In conclusion, we have revealed a non-demethylation role of ALKBH1 in regulating N-glycosylation of LAMPs by interacting with OST subunits and CMA-mediated degradation of HIF-1α.
ALKBH1是一种典型的核酸去甲基化酶,与多种生物过程和人类疾病相关。最近的研究集中在ALKBH1的去甲基化作用上,但其非去甲基化功能却知之甚少。在此,我们证明ALKBH1通过HIF-1α信号通路以一种不依赖去甲基化酶的方式调节糖酵解过程。我们观察到,敲低ALKBH1会抑制糖酵解通量和细胞外酸化,这归因于HIF-1α蛋白水平的降低,而重新引入HIF-1α可以使其恢复。机制上,敲低ALKBH1通过促进HIF-1α与LAMP2A之间的相互作用,增强伴侣介导的自噬(CMA)介导的HIF-1α降解。此外,我们发现ALKBH1与OST48竞争性结合,导致寡糖基转移酶(OST)复合物的结构完整性受损,随后LAMPs(尤其是LAMP2A)的N-糖基化出现缺陷。LAMP2A的异常糖基化破坏了溶酶体稳态,并阻碍了通过CMA对HIF-1α的有效降解。此外,NGI-1是一种选择性靶向OST复合物的小分子抑制剂,它可以抑制由ALKBH1沉默引起的LAMPs糖基化,导致CMA活性受损和溶酶体稳态破坏。总之,我们揭示了ALKBH1在通过与OST亚基相互作用调节LAMPs的N-糖基化以及CMA介导的HIF-1α降解中的非去甲基化作用。