Next Article in Journal
Bicellular Tight Junctions and Wound Healing
Next Article in Special Issue
mRNA-Mediated Duplexes Play Dual Roles in the Regulation of Bidirectional Ribosomal Frameshifting
Previous Article in Journal
Both Intrinsically Disordered Regions and Structural Domains Evolve Rapidly in Immune-Related Mammalian Proteins
Previous Article in Special Issue
Translation Stress Regulates Ribosome Synthesis and Cell Proliferation
Open AccessArticle

Biological and Evolutionary Significance of Terminal Extensions of Mitochondrial Translation Initiation Factor 3

1
Faculty of Biology, M.V. Lomonosov Moscow State University, 119991 Moskva, Russia
2
Institute of Molecular Genetics, Russian Academy of Science, 119991 Moskva, Russia
3
Faculty of Biosciences, Heidelberg University, 69117 Heidelberg, Germany
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Int. J. Mol. Sci. 2018, 19(12), 3861; https://doi.org/10.3390/ijms19123861
Received: 29 October 2018 / Revised: 27 November 2018 / Accepted: 30 November 2018 / Published: 4 December 2018
(This article belongs to the Special Issue Translational Control)
Protein biosynthesis in mitochondria is organized in a bacterial manner. However, during evolution, mitochondrial translation mechanisms underwent many organelle-specific changes. In particular, almost all mitochondrial translation factors, being orthologous to bacterial proteins, are characterized by some unique elements of primary or secondary structure. In the case of the organellar initiation factor 3 (IF3), these elements are several dozen amino acids long N- and C-terminal extensions. This study focused on the terminal extensions of baker’s yeast mitochondrial IF3, Aim23p. By in vivo deletion and complementation analysis, we show that at least one extension is necessary for Aim23p function. At the same time, human mitochondrial IF3 is fully functional in yeast mitochondria even without both terminal extensions. While Escherichia coli IF3 itself is poorly active in yeast mitochondria, adding Aim23p terminal extensions makes the resulting chimeric protein as functional as the cognate factor. Our results show that the terminal extensions of IF3 have evolved as the “adaptors” that accommodate the translation factor of bacterial origin to the evolutionary changed protein biosynthesis system in mitochondria. View Full-Text
Keywords: mitochondria; translation; initiation; initiation factor; terminal extension mitochondria; translation; initiation; initiation factor; terminal extension
Show Figures

Figure 1

MDPI and ACS Style

Derbikova, K.; Kuzmenko, A.; Levitskii, S.; Klimontova, M.; Chicherin, I.; Baleva, M.V.; Krasheninnikov, I.A.; Kamenski, P. Biological and Evolutionary Significance of Terminal Extensions of Mitochondrial Translation Initiation Factor 3. Int. J. Mol. Sci. 2018, 19, 3861.

Show more citation formats Show less citations formats
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

1
Back to TopTop