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<dc:title xml:lang="fr">Etudes des mécanismes d'adressage d'ARN de transfert dans les mitochondries de levure et humaines</dc:title>
<dcterms:alternative xml:lang="en">Study of the mechanisms of tRNA targeting into yeast and human mitochondria</dcterms:alternative>
<dc:subject xml:lang="fr">Mitochondries</dc:subject>
<dc:subject xml:lang="fr">Adressage d’ARN de transfert</dc:subject>
<dc:subject xml:lang="fr">Enolase</dc:subject>
<dc:subject xml:lang="en">Mitochondria</dc:subject>
<dc:subject xml:lang="en">TRNA import</dc:subject>
<dc:subject xml:lang="en">Enolase</dc:subject>
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<tef:elementdEntree autoriteExterne="031445551" autoriteSource="Sudoc">ARN de transfert</tef:elementdEntree>
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<dcterms:abstract xml:lang="fr">Des mutations dans le génome mitochondrial donnent lieu à l’apparition de maladies neuro-dégénératives ou de myopathies. Pour développer des approches de thérapie génique pour prévenir de ces syndromes, nous devons mieux comprendre les mécanismes moléculaires d’import mitochondrial des ARN. Pour cela nous tentons de récapituler in vitro l’import des ARN à partir d’extraits cellulaires fractionnés par différentes méthodes telles que la chromatographie d’exclusion ou d’affinité à l’aide d’étiquettes d’ARN ou de protéines. Nos résultats affinent nos connaissances de ces mécanismes et permettent d’avancer l’idée que l’énolase, une enzyme de la glycolyse, n’agit pas seule lors de la première étape de l’import de l’ARNtLys avec anticodon CUU (tRK1). En effet nous avons montré que l’énolase ultra-purifiée ne se fixait plus à tRK1 in vitro, alors que des préparations de mitochondries de levure récapitulaient l’import lorsque diverses fractions ajoutées à l’énolase étaient testées. Les fractionnements d’extraits opérés permettent de cerner certaines protéines qui pourraient fonctionner de concert avec l’énolase pour véhiculer tRK1 vers la mitochondrie.</dcterms:abstract>
<dcterms:abstract xml:lang="en">Mutations in the mitochondrial genome give rise to neurodegenerative diseases or myopathies. To develop gene therapy for preventing the appearance of these syndromes, we need to better understand the molecular mechanisms of mitochondrial RNA. For this purpose we try to recapitulate in vitro the import of RNA from cell extracts fractionated by different methods such as exclusion or affinity chromatography using tagged RNAs or proteins. Our results refine our knowledge of these mechanisms and allow to advance the idea that enolase, an enzyme of glycolysis, does not act alone during the first stage of import of tRNALys with anticodon CUU (tRK1). Indeed, we have shown that ultra-purified enolase no longer binds to tRK1 in vitro, while preparations of yeast mitochondria recapitulate the import when various fractions mixed with enolase were tested. The performed extracts fractionation make it possible to point to certain proteins which could work in concert with the enolase to convey tRK1 to mitochondria.</dcterms:abstract>
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