期刊
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
卷 23, 期 22, 页码 -出版社
MDPI
DOI: 10.3390/ijms232214241
关键词
mitochondria; translation; translation regulation
资金
- Russian Science Foundation [21-14-00008]
- Ministry of Science and Higher Education of the Russian Federation [075-15-2019-1659]
Protein biosynthesis in mitochondria is closely linked to the assembly of inner membrane complexes and must be coordinated with cytosolic translation. The molecular mechanisms underlying mitochondrial translation regulation are not well understood. This study reveals that PTCD2 functions as a translational regulator of another mitochondrially encoded subunit of cytochrome c oxidase, COIII.
Protein biosynthesis in mitochondria is tightly coupled with assembly of inner membrane complexes and therefore must be coordinated with cytosolic translation of the mRNAs corresponding to the subunits which are encoded in the nucleus. Molecular mechanisms underlying the regulation of mitochondrial translation remain unclear despite recent advances in structural biology. Until now, only one translational regulator of protein biosynthesis in mammalian mitochondria is known-protein TACO1, which regulates translation of COI mRNA. Here we describe the function of pentatricopeptide-containing protein PTCD2 as a translational regulator of another mitochondrially encoded subunit of cytochrome c oxidase-COIII in the HeLa cell line. Deletion of the PTCD2 gene leads to significant decrease in COIII translation efficiency and impairment in CIV activity. Additionally, we show that PTCD2 protein is partially co-sedimentates with associated mitochondrial ribosome and associates with mitochondrial ribosome proteins in pull-down assays. These data allow concluding that PTCD2 is a specific translational regulator of COIII which attracts the mRNA to the mitochondrial ribosome.
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