Department of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, KS, United States of America.
Division of Pharmaceutical Sciences, University of Wisconsin-Madison, Madison, WI, United States of America.
PLoS Genet. 2020 Apr 22;16(4):e1008700. doi: 10.1371/journal.pgen.1008700. eCollection 2020 Apr.
The inability to remove protein aggregates in post-mitotic cells such as muscles or neurons is a cellular hallmark of aging cells and is a key factor in the initiation and progression of protein misfolding diseases. While protein aggregate disorders share common features, the molecular level events that culminate in abnormal protein accumulation cannot be explained by a single mechanism. Here we show that loss of the serine/threonine kinase NUAK causes cellular degeneration resulting from the incomplete clearance of protein aggregates in Drosophila larval muscles. In NUAK mutant muscles, regions that lack the myofibrillar proteins F-actin and Myosin heavy chain (MHC) instead contain damaged organelles and the accumulation of select proteins, including Filamin (Fil) and CryAB. NUAK biochemically and genetically interacts with Drosophila Starvin (Stv), the ortholog of mammalian Bcl-2-associated athanogene 3 (BAG3). Consistent with a known role for the co-chaperone BAG3 and the Heat shock cognate 71 kDa (HSC70)/HSPA8 ATPase in the autophagic clearance of proteins, RNA interference (RNAi) of Drosophila Stv, Hsc70-4, or autophagy-related 8a (Atg8a) all exhibit muscle degeneration and muscle contraction defects that phenocopy NUAK mutants. We further demonstrate that Fil is a target of NUAK kinase activity and abnormally accumulates upon loss of the BAG3-Hsc70-4 complex. In addition, Ubiquitin (Ub), ref(2)p/p62, and Atg8a are increased in regions of protein aggregation, consistent with a block in autophagy upon loss of NUAK. Collectively, our results establish a novel role for NUAK with the Stv-Hsc70-4 complex in the autophagic clearance of proteins that may eventually lead to treatment options for protein aggregate diseases.
在有丝分裂后细胞(如肌肉或神经元)中无法去除蛋白质聚集体是衰老细胞的一个细胞特征,也是蛋白质错误折叠疾病发生和进展的关键因素。虽然蛋白质聚集疾病具有共同特征,但导致异常蛋白质积累的分子水平事件不能用单一机制来解释。在这里,我们显示丝氨酸/苏氨酸激酶 NUAK 的缺失会导致果蝇幼虫肌肉中蛋白质聚集体不完全清除而导致的细胞退化。在 NUAK 突变肌肉中,缺乏肌原纤维蛋白 F-肌动蛋白和肌球蛋白重链 (MHC) 的区域反而包含受损的细胞器和选择蛋白的积累,包括 Filamin (Fil) 和 CryAB。NUAK 在生化和遗传上与果蝇 Starvin (Stv) 相互作用,Stv 是哺乳动物 Bcl-2 相关抗凋亡基因 3 (BAG3) 的同源物。与共伴侣 BAG3 和热休克同源物 71 kDa (HSC70)/HSPA8 ATP 酶在蛋白质自噬清除中的已知作用一致,果蝇 Stv、Hsc70-4 或自噬相关 8a (Atg8a) 的 RNA 干扰 (RNAi) 都表现出肌肉退化和肌肉收缩缺陷,与 NUAK 突变体类似。我们进一步证明 Fil 是 NUAK 激酶活性的靶标,并在 BAG3-Hsc70-4 复合物缺失时异常积累。此外,泛素 (Ub)、ref(2)p/p62 和 Atg8a 在蛋白质聚集区域增加,这与 NUAK 缺失时自噬受阻一致。总之,我们的结果确立了 NUAK 与 Stv-Hsc70-4 复合物在蛋白质自噬清除中的新作用,这可能最终为蛋白质聚集疾病的治疗提供选择。