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1.
Cell Rep ; 29(6): 1728-1738.e9, 2019 11 05.
Article in English | MEDLINE | ID: mdl-31693908

ABSTRACT

Mitochondria harbor specialized ribosomes (mitoribosomes) necessary for the synthesis of key membrane proteins of the oxidative phosphorylation (OXPHOS) machinery located in the mitochondrial inner membrane. To date, no animal model exists to study mitoribosome composition and mitochondrial translation coordination in mammals in vivo. Here, we create MitoRibo-Tag mice as a tool enabling affinity purification and proteomics analyses of mitoribosomes and their interactome in different tissues. We also define the composition of an assembly intermediate formed in the absence of MTERF4, necessary for a late step in mitoribosomal biogenesis. We identify the orphan protein PUSL1, which interacts with a large subunit assembly intermediate, and demonstrate that it is an inner-membrane-associated mitochondrial matrix protein required for efficient mitochondrial translation. This work establishes MitoRibo-Tag mice as a powerful tool to study mitoribosomes in vivo, enabling future studies on the mitoribosome interactome under different physiological states, as well as in disease and aging.


Subject(s)
Mitochondria/metabolism , Mitochondrial Membranes/metabolism , Mitochondrial Proteins/metabolism , Mitochondrial Ribosomes/metabolism , Protein Biosynthesis , Ribosomal Proteins/metabolism , Transcription Factors/metabolism , Animals , GTP-Binding Proteins/genetics , GTP-Binding Proteins/metabolism , Heart/physiology , Kidney/metabolism , Liver/metabolism , Mice , Mice, Transgenic , Mitochondria/genetics , Mitochondrial Proteins/genetics , Myocardium/metabolism , Protein Interaction Maps , Proteome/metabolism , Proteomics , Ribosomal Proteins/genetics , Transcription Factors/genetics
2.
Proc Natl Acad Sci U S A ; 115(41): E9620-E9629, 2018 10 09.
Article in English | MEDLINE | ID: mdl-30249665

ABSTRACT

Mammals develop age-associated clonal expansion of somatic mtDNA mutations resulting in severe respiratory chain deficiency in a subset of cells in a variety of tissues. Both mathematical modeling based on descriptive data from humans and experimental data from mtDNA mutator mice suggest that the somatic mutations are formed early in life and then undergo mitotic segregation during adult life to reach very high levels in certain cells. To address whether mtDNA mutations have a universal effect on aging metazoans, we investigated their role in physiology and aging of fruit flies. To this end, we utilized genetically engineered flies expressing mutant versions of the catalytic subunit of mitochondrial DNA polymerase (DmPOLγA) as a means to introduce mtDNA mutations. We report here that lifespan and health in fruit flies are remarkably tolerant to mtDNA mutations. Our results show that the short lifespan and wide genetic bottleneck of fruit flies are limiting the extent of clonal expansion of mtDNA mutations both in individuals and between generations. However, an increase of mtDNA mutations to very high levels caused sensitivity to mechanical and starvation stress, intestinal stem cell dysfunction, and reduced lifespan under standard conditions. In addition, the effects of dietary restriction, widely considered beneficial for organismal health, were attenuated in flies with very high levels of mtDNA mutations.


Subject(s)
DNA, Mitochondrial , Longevity/genetics , Mutation , Animals , DNA, Mitochondrial/genetics , DNA, Mitochondrial/metabolism , Drosophila melanogaster
3.
Hum Mol Genet ; 26(13): 2515-2525, 2017 07 01.
Article in English | MEDLINE | ID: mdl-28430993

ABSTRACT

Mutations in the mitochondrial DNA polymerase, POLG, are associated with a variety of clinical presentations, ranging from early onset fatal brain disease in Alpers syndrome to chronic progressive external ophthalmoplegia. The majority of mutations are linked with disturbances of mitochondrial DNA (mtDNA) integrity and maintenance. On a molecular level, depending on their location within the enzyme, mutations either lead to mtDNA depletion or the accumulation of multiple mtDNA deletions, and in some cases these molecular changes can be correlated to the clinical presentation. We identified a patient with a dominant p.Y955H mutation in POLG, presenting with a severe, early-onset multi-systemic mitochondrial disease with bilateral sensorineural hearing loss, cataract, myopathy, and liver failure. Using a combination of disease models of Drosophila melanogaster and in vitro biochemistry analysis, we compare the molecular consequences of the p.Y955H mutation to the well-documented p.Y955C mutation. We demonstrate that both mutations affect mtDNA replication and display a dominant negative effect, with the p.Y955H allele resulting in a more severe polymerase dysfunction.


Subject(s)
DNA-Directed DNA Polymerase/genetics , DNA-Directed DNA Polymerase/metabolism , Adult , Amino Acid Sequence , Animals , DNA Polymerase gamma , DNA Replication/genetics , DNA, Mitochondrial/genetics , Disease Models, Animal , Drosophila melanogaster/genetics , Female , Humans , Infant , Mitochondria/genetics , Mutation/genetics , Ophthalmoplegia, Chronic Progressive External/enzymology , Pedigree , Phenotype
4.
Cell Rep ; 16(11): 2980-2990, 2016 09 13.
Article in English | MEDLINE | ID: mdl-27626666

ABSTRACT

Mutations of mtDNA are an important cause of human disease, but few animal models exist. Because mammalian mitochondria cannot be transfected, the development of mice with pathogenic mtDNA mutations has been challenging, and the main strategy has therefore been to introduce mutations found in cell lines into mouse embryos. Here, we describe a phenotype-driven strategy that is based on detecting clonal expansion of pathogenic mtDNA mutations in colonic crypts of founder mice derived from heterozygous mtDNA mutator mice. As proof of concept, we report the generation of a mouse line transmitting a heteroplasmic pathogenic mutation in the alanine tRNA gene of mtDNA displaying typical characteristics of classic mitochondrial disease. In summary, we describe a straightforward and technically simple strategy based on mouse breeding and histology to generate animal models of mtDNA-mutation disease, which will be of great importance for studies of disease pathophysiology and preclinical treatment trials.


Subject(s)
DNA, Mitochondrial/genetics , Mitochondrial Diseases/genetics , Mutation/genetics , Animals , Breeding , Cardiomyopathies/genetics , Cardiomyopathies/physiopathology , Clone Cells , Disease Models, Animal , Female , Mice, Inbred C57BL , Mitochondrial Diseases/physiopathology , Phenotype , Protein Biosynthesis , RNA, Transfer, Ala/genetics
5.
Cell Rep ; 16(9): 2387-98, 2016 08 30.
Article in English | MEDLINE | ID: mdl-27545886

ABSTRACT

Mitochondrial respiratory chain (MRC) complexes I, III, and IV associate into a variety of supramolecular structures known as supercomplexes and respirasomes. While COX7A2L was originally described as a supercomplex-specific factor responsible for the dynamic association of complex IV into these structures to adapt MRC function to metabolic variations, this role has been disputed. Here, we further examine the functional significance of COX7A2L in the structural organization of the mammalian respiratory chain. As in the mouse, human COX7A2L binds primarily to free mitochondrial complex III and, to a minor extent, to complex IV to specifically promote the stabilization of the III2+IV supercomplex without affecting respirasome formation. Furthermore, COX7A2L does not affect the biogenesis, stabilization, and function of the individual oxidative phosphorylation complexes. These data show that independent regulatory mechanisms for the biogenesis and turnover of different MRC supercomplex structures co-exist.


Subject(s)
Electron Transport Complex III/metabolism , Electron Transport Complex IV/metabolism , Electron Transport Complex I/metabolism , Mitochondria, Heart/metabolism , Mitochondrial Membranes/metabolism , Oxidative Phosphorylation , Animals , Electron Transport , Electron Transport Complex I/genetics , Electron Transport Complex III/genetics , Electron Transport Complex IV/genetics , Gene Expression , HEK293 Cells , HeLa Cells , Humans , Mice , Mitochondria, Heart/chemistry , Myocardium/cytology , Myocardium/metabolism , Protein Binding , Protein Stability
6.
PLoS Genet ; 12(5): e1006028, 2016 05.
Article in English | MEDLINE | ID: mdl-27176048

ABSTRACT

Polyadenylation has well characterised roles in RNA turnover and translation in a variety of biological systems. While polyadenylation on mitochondrial transcripts has been suggested to be a two-step process required to complete translational stop codons, its involvement in mitochondrial RNA turnover is less well understood. We studied knockdown and knockout models of the mitochondrial poly(A) polymerase (MTPAP) in Drosophila melanogaster and demonstrate that polyadenylation of mitochondrial mRNAs is exclusively performed by MTPAP. Further, our results show that mitochondrial polyadenylation does not regulate mRNA stability but protects the 3' terminal integrity, and that despite a lack of functioning 3' ends, these trimmed transcripts are translated, suggesting that polyadenylation is not required for mitochondrial translation. Additionally, loss of MTPAP leads to reduced steady-state levels and disturbed maturation of tRNACys, indicating that polyadenylation in mitochondria might be important for the stability and maturation of specific tRNAs.


Subject(s)
Drosophila melanogaster/genetics , Polyadenylation/genetics , Protein Biosynthesis/genetics , RNA, Messenger/genetics , Animals , Codon, Terminator , Gene Knockdown Techniques , Mitochondria/genetics , Mitochondrial Proteins/biosynthesis , Mitochondrial Proteins/genetics , RNA, Mitochondrial , RNA, Transfer/genetics
7.
Nat Commun ; 6: 8808, 2015 Nov 10.
Article in English | MEDLINE | ID: mdl-26554610

ABSTRACT

Replication errors are the main cause of mitochondrial DNA (mtDNA) mutations and a compelling approach to decrease mutation levels would therefore be to increase the fidelity of the catalytic subunit (POLγA) of the mtDNA polymerase. Here we genomically engineer the tamas locus, encoding fly POLγA, and introduce alleles expressing exonuclease- (exo(-)) and polymerase-deficient (pol(-)) POLγA versions. The exo(-) mutant leads to accumulation of point mutations and linear deletions of mtDNA, whereas pol(-) mutants cause mtDNA depletion. The mutant tamas alleles are developmentally lethal but can complement each other in trans resulting in viable flies with clonally expanded mtDNA mutations. Reconstitution of human mtDNA replication in vitro confirms that replication is a highly dynamic process where POLγA goes on and off the template to allow complementation during proofreading and elongation. The created fly models are valuable tools to study germ line transmission of mtDNA and the pathophysiology of POLγA mutation disease.


Subject(s)
DNA, Mitochondrial/genetics , DNA-Directed DNA Polymerase/metabolism , Drosophila/genetics , Exodeoxyribonucleases/metabolism , Genetic Engineering , Animals , DNA Polymerase gamma , DNA-Directed DNA Polymerase/genetics , Exodeoxyribonucleases/genetics , Mutagenesis, Site-Directed , Mutation , Protein Subunits
8.
Nucleic Acids Res ; 42(22): 13920-38, 2014 Dec 16.
Article in English | MEDLINE | ID: mdl-25428350

ABSTRACT

Members of the pentatricopeptide repeat domain (PPR) protein family bind RNA and are important for post-transcriptional control of organelle gene expression in unicellular eukaryotes, metazoans and plants. They also have a role in human pathology, as mutations in the leucine-rich PPR-containing (LRPPRC) gene cause severe neurodegeneration. We have previously shown that the mammalian LRPPRC protein and its Drosophila melanogaster homolog DmLRPPRC1 (also known as bicoid stability factor) are necessary for mitochondrial translation by controlling stability and polyadenylation of mRNAs. We here report characterization of DmLRPPRC2, a second fruit fly homolog of LRPPRC, and show that it has a predominant mitochondrial localization and interacts with a stem-loop interacting RNA binding protein (DmSLIRP2). Ubiquitous downregulation of DmLrpprc2 expression causes respiratory chain dysfunction, developmental delay and shortened lifespan. Unexpectedly, decreased DmLRPPRC2 expression does not globally affect steady-state levels or polyadenylation of mitochondrial transcripts. However, some mitochondrial transcripts abnormally associate with the mitochondrial ribosomes and some products are dramatically overproduced and other ones decreased, which, in turn, results in severe deficiency of respiratory chain complexes. The function of DmLRPPRC2 thus seems to be to ensure that mitochondrial transcripts are presented to the mitochondrial ribosomes in an orderly fashion to avoid poorly coordinated translation.


Subject(s)
Drosophila Proteins/physiology , Mitochondria/genetics , Mitochondrial Proteins/physiology , Protein Biosynthesis , Animals , Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Drosophila melanogaster/genetics , Drosophila melanogaster/growth & development , Drosophila melanogaster/metabolism , Electron Transport , Longevity , Mitochondrial Proteins/genetics , Mitochondrial Proteins/metabolism , Polyadenylation , RNA/metabolism , RNA Interference , RNA, Mitochondrial , Transcription, Genetic
9.
J Clin Invest ; 123(3): 951-7, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23454757

ABSTRACT

Over the last decade, accumulating evidence has suggested a causative link between mitochondrial dysfunction and major phenotypes associated with aging. Somatic mitochondrial DNA (mtDNA) mutations and respiratory chain dysfunction accompany normal aging, but the first direct experimental evidence that increased mtDNA mutation levels contribute to progeroid phenotypes came from the mtDNA mutator mouse. Recent evidence suggests that increases in aging-associated mtDNA mutations are not caused by damage accumulation, but rather are due to clonal expansion of mtDNA replication errors that occur during development. Here we discuss the caveats of the traditional mitochondrial free radical theory of aging and highlight other possible mechanisms, including insulin/IGF-1 signaling (IIS) and the target of rapamycin pathways, that underlie the central role of mitochondria in the aging process.


Subject(s)
Aging/metabolism , Mitochondria/physiology , Aging/genetics , Animals , Cellular Senescence , DNA, Mitochondrial/genetics , Free Radicals/metabolism , Humans , Mitochondria/metabolism , Mutagenesis , Mutation , Signal Transduction
10.
PLoS Genet ; 9(1): e1003178, 2013.
Article in English | MEDLINE | ID: mdl-23300484

ABSTRACT

Regulation of mitochondrial DNA (mtDNA) expression is critical for the control of oxidative phosphorylation in response to physiological demand, and this regulation is often impaired in disease and aging. We have previously shown that mitochondrial transcription termination factor 3 (MTERF3) is a key regulator that represses mtDNA transcription in the mouse, but its molecular mode of action has remained elusive. Based on the hypothesis that key regulatory mechanisms for mtDNA expression are conserved in metazoans, we analyzed Mterf3 knockout and knockdown flies. We demonstrate here that decreased expression of MTERF3 not only leads to activation of mtDNA transcription, but also impairs assembly of the large mitochondrial ribosomal subunit. This novel function of MTERF3 in mitochondrial ribosomal biogenesis is conserved in the mouse, thus we identify a novel and unexpected role for MTERF3 in coordinating the crosstalk between transcription and translation for the regulation of mammalian mtDNA gene expression.


Subject(s)
Drosophila Proteins , Drosophila melanogaster/genetics , Mitochondria , Mitochondrial Proteins , Ribosomes , Animals , DNA, Mitochondrial/genetics , Drosophila Proteins/genetics , Gene Expression Regulation , Invertebrates/genetics , Invertebrates/metabolism , Mice , Mitochondria/genetics , Mitochondria/metabolism , Mitochondrial Proteins/genetics , Oxidative Phosphorylation , Ribosomes/genetics , Ribosomes/metabolism , Transcription, Genetic
11.
EMBO J ; 31(2): 443-56, 2012 Jan 18.
Article in English | MEDLINE | ID: mdl-22045337

ABSTRACT

Regulation of mtDNA expression is critical for maintaining cellular energy homeostasis and may, in principle, occur at many different levels. The leucine-rich pentatricopeptide repeat containing (LRPPRC) protein regulates mitochondrial mRNA stability and an amino-acid substitution of this protein causes the French-Canadian type of Leigh syndrome (LSFC), a neurodegenerative disorder characterized by complex IV deficiency. We have generated conditional Lrpprc knockout mice and show here that the gene is essential for embryonic development. Tissue-specific disruption of Lrpprc in heart causes mitochondrial cardiomyopathy with drastic reduction in steady-state levels of most mitochondrial mRNAs. LRPPRC forms an RNA-dependent protein complex that is necessary for maintaining a pool of non-translated mRNAs in mammalian mitochondria. Loss of LRPPRC does not only decrease mRNA stability, but also leads to loss of mRNA polyadenylation and the appearance of aberrant mitochondrial translation. The translation pattern without the presence of LRPPRC is misregulated with excessive translation of some transcripts and no translation of others. Our findings point to the existence of an elaborate machinery that regulates mammalian mtDNA expression at the post-transcriptional level.


Subject(s)
Cytochrome-c Oxidase Deficiency/genetics , Leigh Disease/genetics , Mitochondria, Heart/physiology , Neoplasm Proteins/physiology , Polyadenylation/physiology , Protein Biosynthesis/physiology , Animals , DNA, Mitochondrial/genetics , Electron Transport Complex IV/analysis , HeLa Cells , Humans , Macromolecular Substances , Mice , Mice, Knockout , Neoplasm Proteins/deficiency , Neoplasm Proteins/genetics , Organ Specificity , Polynucleotide Adenylyltransferase , RNA Stability , RNA, Messenger , RNA-Binding Proteins/metabolism
12.
PLoS Genet ; 7(10): e1002324, 2011 Oct.
Article in English | MEDLINE | ID: mdl-22022283

ABSTRACT

The bicoid stability factor (BSF) of Drosophila melanogaster has been reported to be present in the cytoplasm, where it stabilizes the maternally contributed bicoid mRNA and binds mRNAs expressed from early zygotic genes. BSF may also have other roles, as it is ubiquitously expressed and essential for survival of adult flies. We have performed immunofluorescence and cell fractionation analyses and show here that BSF is mainly a mitochondrial protein. We studied two independent RNAi knockdown fly lines and report that reduced BSF protein levels lead to a severe respiratory deficiency and delayed development at the late larvae stage. Ubiquitous knockdown of BSF results in a severe reduction of the polyadenylation tail lengths of specific mitochondrial mRNAs, accompanied by an enrichment of unprocessed polycistronic RNA intermediates. Furthermore, we observed a significant reduction in mRNA steady state levels, despite increased de novo transcription. Surprisingly, mitochondrial de novo translation is increased and abnormal mitochondrial translation products are present in knockdown flies, suggesting that BSF also has a role in coordinating the mitochondrial translation in addition to its role in mRNA maturation and stability. We thus report a novel function of BSF in flies and demonstrate that it has an important intra-mitochondrial role, which is essential for maintaining mtDNA gene expression and oxidative phosphorylation.


Subject(s)
Drosophila Proteins/genetics , Drosophila melanogaster/growth & development , Drosophila melanogaster/genetics , Mitochondria/genetics , Polyadenylation/genetics , RNA, Messenger/genetics , RNA-Binding Proteins/genetics , Animals , Body Weight/genetics , Drosophila Proteins/metabolism , Drosophila melanogaster/physiology , Fertility/genetics , Gene Expression Regulation, Developmental , Gene Knockdown Techniques , Mitochondria/physiology , Mitochondrial Proteins/genetics , Mitochondrial Proteins/metabolism , Oxidative Phosphorylation , Phylogeny , Protein Biosynthesis , RNA Interference , RNA-Binding Proteins/metabolism
13.
J Agric Food Chem ; 58(6): 3488-94, 2010 Mar 24.
Article in English | MEDLINE | ID: mdl-20187605

ABSTRACT

The protective role in vivo of buckwheat metallothionein type 3 (FeMT3) during metal stress and the responsiveness of its promoter to metal ions were examined. Increased tolerance to heavy metals of FeMT3 producing Escherichia coli and cup1(Delta) yeast cells was detected. The defensive ability of buckwheat MT3 during Cd and Cu stresses was also demonstrated in Nicotiana debneyii leaves transiently expressing FeMT3. In contrast to phytochelatins, the cytoplasmatic localization of FeMT3 was not altered under heavy metal stress. Functional analysis of the corresponding promoter region revealed extremely high inducibility upon Cu(2+) and Cd(2+) treatments. The confirmed defense ability of FeMT3 protein in vivo and the great responsiveness of its promoter during heavy metal exposure make this gene a suitable candidate for biotechnological applications.


Subject(s)
Fagopyrum/genetics , Gene Expression Regulation, Plant , Metals, Heavy/metabolism , Nerve Tissue Proteins/metabolism , Plant Proteins/metabolism , Promoter Regions, Genetic , Amino Acid Sequence , Cadmium/metabolism , Copper/metabolism , Fagopyrum/chemistry , Metallothionein 3 , Molecular Sequence Data , Nerve Tissue Proteins/chemistry , Nerve Tissue Proteins/genetics , Plant Proteins/chemistry , Plant Proteins/genetics , Sequence Alignment , Nicotiana/genetics , Nicotiana/metabolism
14.
J Plant Physiol ; 166(9): 996-1000, 2009 Jun 01.
Article in English | MEDLINE | ID: mdl-19185389

ABSTRACT

To shed light on expression regulation of the metallothionein gene from buckwheat (FeMT3), functional promoter analysis was performed with a complete 5' regulatory region and two deletion variants, employing stably transformed tobacco plants. Histochemical GUS assay of transgenic tobacco lines showed the strongest signals in vascular elements of leaves and in pollen grains, while somewhat weaker staining was observed in the roots of mature plants. This tissue specificity pattern implies a possible function of buckwheat MT3 in those tissues. Quantitative GUS assay showed strong up-regulation of all three promoter constructs (proportional to the length of the regulatory region) in leaves submerged in liquid MS medium containing sucrose, after a prolonged time period. This represented a complex stress situation composed of several synergistically related stress stimuli. These findings suggest complex transcriptional regulation of FeMT3, requiring interactions among a number of different factors.


Subject(s)
Fagopyrum/genetics , Metallothionein/genetics , Promoter Regions, Genetic/genetics , Gene Expression Regulation, Plant/drug effects , Plants, Genetically Modified/genetics , Sucrose/pharmacology , Nicotiana/genetics
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