https://ror.org/03zga2b32 Department of Biomedicine, University of Bergen, Bergen, Norway
Genes and Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Life Sci Alliance. 2024 Oct 9;7(12). doi: 10.26508/lsa.202402795. Print 2024 Dec.
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 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 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.
肌动蛋白是真核细胞骨架的关键组成部分。在动物中,肌动蛋白通过专门的酶进行独特的 N 端加工,形成成熟的酸性和乙酰化形式。最后一步,N 端乙酰化,由人类的 NAA80 催化。肌动蛋白的 N 端乙酰化对于维持人类细胞系中正常的细胞骨架动态和细胞迁移至关重要。然而,肌动蛋白 N 端乙酰化的生理影响仍有待充分理解。我们开发了一种斑马鱼敲除模型,并证明 Naa80 在体内对肌动蛋白和非肌动蛋白进行乙酰化。用纯化的 Naa80 进行的测定显示出对肌动蛋白 N 端的优先乙酰化。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。相比之下,患有致病性肌动蛋白变体的人类可能表现出张力减退和听力障碍。虽然缺乏 的斑马鱼没有明显的肌肉缺陷或异常,但我们观察到内耳发育异常、小耳石和对声音的反应受损。总之,我们已经确定,斑马鱼 Naa80 在体外和体内将肌动蛋白 N 端乙酰化,并且肌动蛋白 N 端乙酰化对于正常听力是必需的。