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<dc:title xml:lang="fr">Entre cycle cellulaire et réponse aux dommages à l'ADN : fonctions de la protéine F-box FBL17 chez Arabidopsis thaliana</dc:title>
<dcterms:alternative xml:lang="en">Between cell cycle regulation and DNA damage response : functions of the F-box protein FBL17 in Arabidopsis thaliana</dcterms:alternative>
<dc:subject xml:lang="fr">F-box</dc:subject>
<dc:subject xml:lang="fr">Cycle cellulaire</dc:subject>
<dc:subject xml:lang="fr">Réponse aux dommages à l’ADN</dc:subject>
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<dcterms:abstract xml:lang="fr">La protéine F-box FBL17 est un régulateur clef de la progression du cycle cellulaire chez Arabidopsis thaliana. Elle est notamment impliquée dans la dégradation des protéines inhibitrices de CDK, ce qui conduit chez le mutant fbl17 à des phénotypes développementaux sévères et une réduction drastique de l'activité de division cellulaire dans les méristèmes. Si l’implication de FBL17 dans le cycle cellulaire a été bien caractérisée, son répertoire de substrats et ses autres fonctions biologiques restent encore méconnus. Durant cette thèse, l’interactome de FBL17 a été mis en évidence et son implication dans la réponse aux dommages à l’ADN (DDR) a été étudiée. Le mutant fbl17 présente une DDR constitutive associée à une augmentation du nombre de lésions de l’ADN, et l’induction de gènes de la DDR de façon SOG1-indépendante. Au niveau protéique, en condition de stress génotoxique, FBL17 est recrutée au niveau des sites de lésions de l’ADN où elle co-localise avec la protéine RBR1. Ces données supportent un rôle de FBL17 dans le maintien de l’intégrité génétique des cellules.</dcterms:abstract>
<dcterms:abstract xml:lang="en">In Arabidopsis thaliana, the F-box protein FBL17 is a key regulator of the cell cycle. FBL17 is especially implicated in the degradation of CDK inhibitor protein, which result in strong developmental phenotypes in fbl17 loss-of-function mutants, as well as a drastic reduction of cell division activity in meristems. While FBL17 involvement in cell cycle has been well described, its whole substrate’s repertoire and its other biological implications remain poorly understood. During this PhD, the FBL17 interactome has been established and its implication in DNA damage response (DDR) has been demonstrated. The fbl17 mutant presents a constitutive DDR associated with a higher frequency of DNA lesions and the induction of DDR genes in a SOG1-independant manner. At the protein level, upon genotoxic stress, FBL17 protein is recruited at DNA lesion sites where it colocalizes with RBR1. All these data support the implication of FBL17 in the maintenance of cell genome integrity.</dcterms:abstract>
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