Rasmus Ree, Sheng-Jia Lin, Lars Ole Sti Dahl, Kevin Huang, Cassidy Petree, Gaurav K Varshney, Thomas Arnesen
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引用次数: 0
摘要
肌动蛋白是真核细胞骨架的重要组成部分。在动物体内,肌动蛋白通过专用酶进行独特的 N 端加工,形成成熟的酸性和乙酰化形式。最后一步,即 N 端乙酰化,在人类中由 NAA80 催化。在人类细胞系中,肌动蛋白的 N 端乙酰化对于维持正常的细胞骨架动态和细胞运动至关重要。然而,肌动蛋白 N 端乙酰化的生理影响仍有待充分了解。我们建立了斑马鱼 Naa80 基因敲除模型,并证明 Naa80 在体内可对肌肉和非肌肉肌动蛋白进行乙酰化。用纯化的 Naa80 进行的检测显示,Naa80 更倾向于乙酰化肌动蛋白的 N-端。缺乏肌动蛋白 N 端乙酰化的斑马鱼表现出正常的发育、形态和行为。与此相反,具有致病性肌动蛋白变体的人类会出现肌张力低下和听力障碍。虽然缺乏naa80的斑马鱼没有表现出明显的肌肉缺陷或异常,但我们观察到内耳发育异常、耳石变小以及对声音的反应受损。总之,我们已经确定斑马鱼 Naa80 N 端在体外和体内乙酰化肌动蛋白,而肌动蛋白 N 端乙酰化对正常听力至关重要。
Naa80 is required for actin N-terminal acetylation and normal hearing in zebrafish.
Actin is a critical component of the eukaryotic cytoskeleton. In animals, actins undergo unique N-terminal processing by dedicated enzymes resulting in mature acidic and acetylated forms. The final step, N-terminal acetylation, is catalyzed by NAA80 in humans. N-terminal acetylation of actin is crucial for maintaining normal cytoskeletal dynamics and cell motility in human cell lines. However, the physiological impact of actin N-terminal acetylation remains to be fully understood. We developed a zebrafish naa80 knockout model and demonstrated that Naa80 acetylates both muscle and non-muscle actins in vivo. Assays with purified Naa80 revealed a preference for acetylating actin N-termini. Zebrafish lacking actin N-terminal acetylation exhibited normal development, morphology, and behavior. In contrast, humans with pathogenic actin variants can present with hypotonia and hearing impairment. Whereas zebrafish lacking naa80 showed no obvious muscle defects or abnormalities, we observed abnormal inner ear development, small otoliths, and impaired response to sound. In conclusion, we have established that zebrafish Naa80 N-terminally acetylates actins in vitro and in vivo, and that actin N-terminal acetylation is essential for normal hearing.
期刊介绍:
Life Science Alliance is a global, open-access, editorially independent, and peer-reviewed journal launched by an alliance of EMBO Press, Rockefeller University Press, and Cold Spring Harbor Laboratory Press. Life Science Alliance is committed to rapid, fair, and transparent publication of valuable research from across all areas in the life sciences.