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<dc:title xml:lang="en">The role of SAGA deubiquitinase module in transcriptional regulation</dc:title>
<dcterms:alternative xml:lang="fr">Le rôle du module de deubiquitination SAGA dans la régulation de la transcription</dcterms:alternative>
<dc:subject xml:lang="fr">Régulation transcriptionnelle</dc:subject>
<dc:subject xml:lang="fr">Développement embryonnaire</dc:subject>
<dc:subject xml:lang="fr">ATXN7L3</dc:subject>
<dc:subject xml:lang="fr">H2Bub1</dc:subject>
<dc:subject xml:lang="fr">Pol II</dc:subject>
<dc:subject xml:lang="en">Transcriptional regulation</dc:subject>
<dc:subject xml:lang="en">Embryonic development</dc:subject>
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<dcterms:abstract xml:lang="fr">L’ensemble des protéines du DUBm de SAGA sont requises pour le clivage de molécules d’histones H2Bub1, nous étudions le rôle du DUBm de SAGA dans la régulation de la transcription. Nous avons démontré que la protéine ATXN7L3 est essentielle pour le développement embryonnaire. Pour avoir un meilleur aperçu de la fonction d’ATXN7L3, nous avons effectué des expériences de différentiation de mESC en l’absence d’ATXN7L3. Nous avons observé qu’ATXN7L3 promeut la différenciation des mESC en cardiomyocytes, mais pas en précurseurs de l’ectoderme neural. De ce fait, ATNX7L3 pourrait fonctionner de manière tissue-spécifique. En outre, nous avons effectué des analyses transcriptionnelles et ChIP-seq de mESC Atxn7l3-/-. De façon inattendue, les niveaux de H2Bub1 sont significativement plus élevés dans le corps de l’ensemble des gènes transcrits en l’absence d’ATXN7L3. Cependant, l’occupation de l’ARN polymérase II sur l’ensemble de ces gènes ne varie que modestement dans ces cellules Atxn7l3-/-. Ainsi, la déubiquitination de H2Bub1 ne régule pas directement la transcription par l’ARN polymérase II de l’ensemble du génome.</dcterms:abstract>
<dcterms:abstract xml:lang="en">The deubiquitylation module of SAGA is required for the removal of mono-ubiquitin from histone H2B. Here we investigated the role of SAGA deubiquitinase module in transcriptional regulation. We found that Atxn7l3 is essential for embryonic development. To get better insight into ATXN7L3, we carried out mESC differentiation assays. Our results showed that ATXN7L3 promoted the differentiation of cardiomyocyte cells, but not ectoderm neural precursor. Thereby, ATXN7L3 might function in a tissue-specific manner. To understand the molecular mechanisms underlying these phenotypes, we performed transcriptomic and ChIP-Seq analyses from Atxn7l3-/- mESC. Unexpectedly, although H2Bub1 levels significantly increased in the gene body of every expressed gene, the genome-wide occupancy of Pol II was only modestly changed in Atxn7l3-/- mESCs. Thus, H2Bub1 deubiquitination did not directly regulate global Pol II transcription.</dcterms:abstract>
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</mets:mets>