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从近期的结构研究中洞察线粒体核糖体的生物发生。

Insights into mitoribosomal biogenesis from recent structural studies.

机构信息

Department of Medical Biochemistry and Biophysics, Division of Molecular Metabolism, Karolinska Institutet, Biomedicum, 171 65 Solna, Sweden; Max Planck Institute Biology of Ageing, Karolinska Institutet Laboratory, Karolinska Institutet, Stockholm, Sweden.

Department of Medical Biochemistry and Biophysics, Division of Molecular Metabolism, Karolinska Institutet, Biomedicum, 171 65 Solna, Sweden; Max Planck Institute Biology of Ageing, Karolinska Institutet Laboratory, Karolinska Institutet, Stockholm, Sweden.

出版信息

Trends Biochem Sci. 2023 Jul;48(7):629-641. doi: 10.1016/j.tibs.2023.04.002. Epub 2023 May 10.

Abstract

The mitochondrial ribosome (mitoribosome) is a multicomponent machine that has unique structural features. Biogenesis of the human mitoribosome includes correct maturation and folding of the mitochondria-encoded RNA components (12S and 16S mt-rRNAs, and mt-tRNAVal) and their assembly together with 82 nucleus-encoded mitoribosomal proteins. This complex process requires the coordinated action of multiple assembly factors. Recent advances in single-particle cryo-electron microscopy (cryo-EM) have provided detailed insights into the specific functions of several mitoribosome assembly factors and have defined their timing. In this review we summarize mitoribosomal small (mtSSU) and large subunit (mtLSU) biogenesis based on structural findings, and we discuss potential crosstalk between mtSSU and mtLSU assembly pathways as well as coordination between mitoribosome biogenesis and other processes involved in mitochondrial gene expression.

摘要

线粒体核糖体(mitoribosome)是一种具有独特结构特征的多组分机器。人类线粒体核糖体的生物发生包括线粒体编码的 RNA 成分(12S 和 16S mt-rRNAs 和 mt-tRNAVal)的正确成熟和折叠,以及它们与 82 种核编码的线粒体核糖体蛋白一起组装。这个复杂的过程需要多个组装因子的协调作用。单颗粒冷冻电子显微镜(cryo-EM)的最新进展为几个线粒体核糖体组装因子的特定功能提供了详细的见解,并确定了它们的时间。在这篇综述中,我们根据结构发现总结了线粒体核糖体小亚基(mtSSU)和大亚基(mtLSU)的生物发生,并讨论了 mtSSU 和 mtLSU 组装途径之间的潜在串扰以及线粒体核糖体生物发生与线粒体基因表达涉及的其他过程之间的协调。

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