Lopez Sanchez Maria Isabel G, Krüger Annika, Shiriaev Dmitrii I, Liu Yong, Rorbach Joanna
Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, 32 Gisborne Street, East Melbourne, VIC 3002, Australia.
Department of Medical Biochemistry and Biophysics, Division of Molecular Metabolism, Karolinska Institutet, Solnavägen 9, 171 65 Stockholm, Sweden.
Int J Mol Sci. 2021 Apr 7;22(8):3827. doi: 10.3390/ijms22083827.
Mammalian mitochondrial ribosomes (mitoribosomes) synthesize a small subset of proteins, which are essential components of the oxidative phosphorylation machinery. Therefore, their function is of fundamental importance to cellular metabolism. The assembly of mitoribosomes is a complex process that progresses through numerous maturation and protein-binding events coordinated by the actions of several assembly factors. Dysregulation of mitoribosome production is increasingly recognized as a contributor to metabolic and neurodegenerative diseases. In recent years, mutations in multiple components of the mitoribosome assembly machinery have been associated with a range of human pathologies, highlighting their importance to cell function and health. Here, we provide a review of our current understanding of mitoribosome biogenesis, highlighting the key factors involved in this process and the growing number of mutations in genes encoding mitoribosomal RNAs, proteins, and assembly factors that lead to human disease.
哺乳动物线粒体核糖体(线粒体核糖体)合成一小部分蛋白质,这些蛋白质是氧化磷酸化机制的重要组成部分。因此,它们的功能对细胞代谢至关重要。线粒体核糖体的组装是一个复杂的过程,通过多个成熟和蛋白质结合事件进行,这些事件由几种组装因子的作用协调。线粒体核糖体产生的失调越来越被认为是代谢和神经退行性疾病的一个促成因素。近年来,线粒体核糖体组装机制的多个组成部分的突变与一系列人类疾病相关,突出了它们对细胞功能和健康的重要性。在这里,我们综述了我们目前对线粒体核糖体生物发生的理解,强调了这一过程中涉及的关键因素,以及编码线粒体核糖体RNA、蛋白质和组装因子的基因中导致人类疾病的突变数量不断增加。