Rathore Sorbhi, Conrad Julian, De Silva Dasmanthie, Ferrari Alberto, Bouquio Danielle, Kim Hyung-Jun, Salvatori Roger, Linden Andreas, Dybkov Olexandr, Urlaub Henning, Ott Martin, Barrientos Antoni
Department of Biochemistry and Biophysics, Stockholm University. Stockholm SE-10691, Sweden.
Department of Biochemistry and Biophysics, Stockholm University. Stockholm SE-10691, Sweden; Science for Life Laboratory, Stockholm University, Solna SE-10691, Sweden.
Biochim Biophys Acta Mol Cell Res. 2025 Aug 25;1872(8):120051. doi: 10.1016/j.bbamcr.2025.120051.
The Saccharomyces cerevisiae mitoribosome synthesizes eight mitochondrial DNA-encoded proteins essential for oxidative phosphorylation. Mitoribosome large subunit (mtLSU) biogenesis involves the conserved DEAD-box helicase Mrh4 and the GTPases Mtg1/GTPBP7 and Mtg2/GTPBP5. Here, we have employed genetic, biochemical, in vitro reconstitution, and cryo-EM approaches to elucidate their hierarchical action during the late stages of mtLSU assembly. We show that Mrh4-mediated bL33m incorporation precedes Mtg1 recruitment to the 21S rRNA. Cryo-EM structures of mitoribosome assembly intermediates accumulating in the absence of Mtg1 or uL16m reveal that Mtg1 restructures the 21S rRNA H73-75 and H93 domains to their mature fold. This subsequently allows the structuring of neighboring peptidyl transfer center region helices and the incorporation of uL6m, uL16m, bL35m, and bL36m during late mtLSU maturation. Unexpectedly, monosomes containing immature mtLSU assemble in Mrh4-, bL33m-, uL16m-, Mtg1-, and Mtg2-depleted mitochondria, at levels that increase with the maturation state of the mtLSU particle. Our data have shed light on the rRNA folding events and the structuring of the MRPs that occur during the late stages of assembly. They have provided insight into the roles of assembly factors Mrh4, Mtg1, and Mtg2 during the process and revealed evolutionarily conserved mechanisms underlying mitochondrial ribosome assembly.
酿酒酵母线粒体核糖体合成八种对氧化磷酸化至关重要的线粒体DNA编码蛋白。线粒体核糖体大亚基(mtLSU)的生物发生涉及保守的DEAD盒解旋酶Mrh4以及GTP酶Mtg1/GTPBP7和Mtg2/GTPBP5。在这里,我们采用了遗传学、生物化学、体外重建和冷冻电镜方法,以阐明它们在mtLSU组装后期的层级作用。我们表明,Mrh4介导的bL33m掺入先于Mtg1募集到21S rRNA上。在缺乏Mtg1或uL16m的情况下积累的线粒体核糖体组装中间体的冷冻电镜结构表明,Mtg1将21S rRNA的H73 - 75和H93结构域重构成其成熟折叠。这随后允许在mtLSU成熟后期构建相邻的肽基转移中心区域螺旋,并掺入uL6m、uL16m、bL35m和bL36m。出乎意料的是,含有未成熟mtLSU的单体在Mrh4、bL33m、uL16m、Mtg1和Mtg2缺失的线粒体中组装,其水平随着mtLSU颗粒的成熟状态而增加。我们的数据揭示了组装后期发生 的rRNA折叠事件和线粒体核糖体蛋白(MRP)的构建。它们提供了对组装因子Mrh4、Mtg1和Mtg2在此过程中作用的见解,并揭示了线粒体核糖体组装背后的进化保守机制。