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      Stress signaling and cellular proliferation reverse the effects of mitochondrial mistranslation

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          Abstract

          <p id="d392797e615">Translation fidelity is crucial for prokaryotes and eukaryotic nuclear‐encoded proteins; however, little is known about the role of mistranslation in mitochondria and its potential effects on metabolism. We generated yeast and mouse models with error‐prone and hyper‐accurate mitochondrial translation, and found that translation rate is more important than translational accuracy for cell function in mammals. Specifically, we found that mitochondrial mistranslation causes reduced overall mitochondrial translation and respiratory complex assembly rates. In mammals, this effect is compensated for by increased mitochondrial protein stability and upregulation of the citric acid cycle. Moreover, this induced mitochondrial stress signaling, which enables the recovery of mitochondrial translation via mitochondrial biogenesis, telomerase expression, and cell proliferation, and thereby normalizes metabolism. Conversely, we show that increased fidelity of mitochondrial translation reduces the rate of protein synthesis without eliciting a mitochondrial stress response. Consequently, the rate of translation cannot be recovered and this leads to dilated cardiomyopathy in mice. In summary, our findings reveal mammalian‐specific signaling pathways that respond to changes in the fidelity of mitochondrial protein synthesis and affect metabolism. </p><p class="first" id="d392797e618">Error‐prone mitochondrial translation induces a rescuing stress response, while hyper‐accuracy causes dilated cardiomyopathy in mice by reducing protein production without activating compensatory responses. <div class="boxed-text panel" id="embj2019102155-blkfxd-0002"> <a class="named-anchor" id="embj2019102155-blkfxd-0002"> <!-- named anchor --> </a> <div class="figure-container so-text-align-c"> <img alt="" class="figure" src="/document_file/6af0f97d-2d1b-4e33-9db8-e7c52d04f093/PubMedCentral/image/EMBJ-38-e102155-g014.jpg"/> </div> <div class="panel-content"/> </div> </p>

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          Most cited references44

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          Mitochondrial transcription factor A regulates mtDNA copy number in mammals.

          Mitochondrial DNA (mtDNA) copy number regulation is altered in several human mtDNA-mutation diseases and it is also important in a variety of normal physiological processes. Mitochondrial transcription factor A (TFAM) is essential for human mtDNA transcription and we demonstrate here that it is also a key regulator of mtDNA copy number. We initially performed in vitro transcription studies and determined that the human TFAM protein is a poor activator of mouse mtDNA transcription, despite its high capacity for unspecific DNA binding. Next, we generated P1 artificial chromosome (PAC) transgenic mice ubiquitously expressing human TFAM. The introduced human TFAM gene was regulated in a similar fashion as the endogenous mouse Tfam gene and expression of the human TFAM protein in the mouse did not result in down-regulation of the endogenous expression. The PAC-TFAM mice thus had a net overexpression of TFAM protein and this resulted in a general increase of mtDNA copy number. We used a combination of mice with TFAM overexpression and TFAM knockout and demonstrated that mtDNA copy number is directly proportional to the total TFAM protein levels also in mouse embryos. Interestingly, the expression of human TFAM in the mouse results in up-regulation of mtDNA copy number without increasing respiratory chain capacity or mitochondrial mass. It is thus possible to experimentally dissociate mtDNA copy number regulation from mtDNA expression and mitochondrial biogenesis in mammals in vivo. In conclusion, our results provide genetic evidence for a novel role for TFAM in direct regulation of mtDNA copy number in mammals.
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            Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases.

            Mitochondria are eukaryotic organelles that generate most of the energy in the cell by oxidative phosphorylation (OXPHOS). Each mitochondrion contains multiple copies of a closed circular double-stranded DNA genome (mtDNA). Human (mammalian) mtDNA encodes 13 essential subunits of the inner membrane complex responsible for OXPHOS. These mRNAs are translated by the mitochondrial protein synthesis machinery, which uses the 22 species of mitochondrial tRNAs (mt tRNAs) encoded by mtDNA. The unique structural features of mt tRNAs distinguish them from cytoplasmic tRNAs bearing the canonical cloverleaf structure. The genes encoding mt tRNAs are highly susceptible to point mutations, which are a primary cause of mitochondrial dysfunction and are associated with a wide range of pathologies. A large number of nuclear factors involved in the biogenesis and function of mt tRNAs have been identified and characterized, including processing endonucleases, tRNA-modifying enzymes, and aminoacyl-tRNA synthetases. These nuclear factors are also targets of pathogenic mutations linked to various diseases, indicating the functional importance of mt tRNAs for mitochondrial activity.
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              Ribosome. The structure of the human mitochondrial ribosome.

              The highly divergent ribosomes of human mitochondria (mitoribosomes) synthesize 13 essential proteins of oxidative phosphorylation complexes. We have determined the structure of the intact mitoribosome to 3.5 angstrom resolution by means of single-particle electron cryogenic microscopy. It reveals 80 extensively interconnected proteins, 36 of which are specific to mitochondria, and three ribosomal RNA molecules. The head domain of the small subunit, particularly the messenger (mRNA) channel, is highly remodeled. Many intersubunit bridges are specific to the mitoribosome, which adopts conformations involving ratcheting or rolling of the small subunit that are distinct from those seen in bacteria or eukaryotes. An intrinsic guanosine triphosphatase mediates a contact between the head and central protuberance. The structure provides a reference for analysis of mutations that cause severe pathologies and for future drug design. Copyright © 2015, American Association for the Advancement of Science.
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                Author and article information

                Journal
                The EMBO Journal
                EMBO J
                EMBO
                0261-4189
                1460-2075
                August 05 2019
                December 16 2019
                November 13 2019
                December 16 2019
                : 38
                : 24
                Affiliations
                [1 ]Harry Perkins Institute of Medical Research Nedlands WA Australia
                [2 ]The University of Western Australia Centre for Medical Research Crawley WA Australia
                [3 ]Metabolomics Australia Bio21 Institute of Molecular Science and Biotechnology University of Melbourne Parkville Vic. Australia
                [4 ]Centre for Microscopy, Characterisation and Analysis The University of Western Australia Perth WA Australia
                [5 ]School of Molecular Sciences The University of Western Australia, Crawley WA Australia
                [6 ]The School of Biomedical Sciences The University of Western Australia Nedlands WA Australia
                [7 ]School of Human Sciences (Physiology) The University of Western Australia Crawley WA Australia
                [8 ]Victor Chang Cardiac Research Institute Darlinghurst NSW Australia
                [9 ]School of Pharmacy and Biomedical Sciences Curtin University Bentley WA Australia
                [10 ]Curtin Health Innovation Research Institute Curtin University Bentley WA Australia
                Article
                10.15252/embj.2019102155
                6912024
                31721250
                cc8e0e00-cc92-41c8-b2e9-39b017cfb0c4
                © 2019

                http://onlinelibrary.wiley.com/termsAndConditions#am

                http://onlinelibrary.wiley.com/termsAndConditions#vor

                http://doi.wiley.com/10.1002/tdm_license_1.1

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