Department of Biochemistry and Molecular Biology, State University of New York Upstate Medical University, Syracuse, United States.
Institute of Biochemistry and Molecular Biology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Elife. 2023 May 2;12:e84330. doi: 10.7554/eLife.84330.
Mitochondrial biogenesis requires the import of >1,000 mitochondrial preproteins from the cytosol. Most studies on mitochondrial protein import are focused on the core import machinery. Whether and how the biophysical properties of substrate preproteins affect overall import efficiency is underexplored. Here, we show that protein traffic into mitochondria can be disrupted by amino acid substitutions in a single substrate preprotein. Pathogenic missense mutations in ADP/ATP translocase 1 (ANT1), and its yeast homolog ADP/ATP carrier 2 (Aac2), cause the protein to accumulate along the protein import pathway, thereby obstructing general protein translocation into mitochondria. This impairs mitochondrial respiration, cytosolic proteostasis, and cell viability independent of ANT1's nucleotide transport activity. The mutations act synergistically, as double mutant Aac2/ANT1 causes severe clogging primarily at the translocase of the outer membrane (TOM) complex. This confers extreme toxicity in yeast. In mice, expression of a super-clogger ANT1 variant led to neurodegeneration and an age-dependent dominant myopathy that phenocopy ANT1-induced human disease, suggesting clogging as a mechanism of disease. More broadly, this work implies the existence of uncharacterized amino acid requirements for mitochondrial carrier proteins to avoid clogging and subsequent disease.
线粒体生物发生需要将超过 1000 种线粒体前体蛋白从细胞质中输入。大多数关于线粒体蛋白输入的研究都集中在核心输入机制上。底物前体蛋白的物理特性如何影响整体输入效率还未得到充分探索。在这里,我们表明,单个底物前体蛋白中的氨基酸取代可以破坏蛋白质向线粒体的运输。三磷酸腺苷/二磷酸腺苷转运酶 1(ANT1)及其酵母同源物三磷酸腺苷/二磷酸腺苷载体 2(Aac2)中的致病性错义突变会导致该蛋白在线粒体蛋白输入途径中积累,从而阻碍一般蛋白质向线粒体的转运。这会损害线粒体呼吸、细胞质蛋白质稳态和细胞活力,而不依赖于 ANT1 的核苷酸转运活性。这些突变具有协同作用,因为双突变体 Aac2/ANT1 主要在外膜转运体(TOM)复合物处造成严重堵塞。这在酵母中导致了极度的毒性。在小鼠中,表达超级堵塞的 ANT1 变体导致神经退行性变和年龄依赖性显性肌病,与 ANT1 诱导的人类疾病表型相似,表明堵塞是一种疾病机制。更广泛地说,这项工作意味着存在未被表征的氨基酸要求,以避免线粒体载体蛋白堵塞和随后的疾病。