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<dc:title xml:lang="en">Functional study of the coactivator complexes SAGA and ATAC in mouse embryonic stem cells</dc:title>
<dcterms:alternative xml:lang="fr">Etude fonctionnelle des complexes coactivateurs SAGA et ATAC dans les cellules souches de souris</dcterms:alternative>
<dc:subject xml:lang="fr">Histone acétyltransférase</dc:subject>
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<dc:subject xml:lang="fr">Cellules souches embryonnaires de souris</dc:subject>
<dc:subject xml:lang="fr">ARN Polymérase II</dc:subject>
<dc:subject xml:lang="en">Histone acetyltransferase</dc:subject>
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<dc:subject xml:lang="en">SAGA</dc:subject>
<dc:subject xml:lang="en">Mouse embryonic stem cells</dc:subject>
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<dcterms:abstract xml:lang="fr">Des études récentes de mon laboratoire d’accueil indiquent que le complexe de modification des histones SAGA agit comme un cofacteur général pour la transcription par l’ARN polymérase II dans la levure, contrairement à sa fonction spécifique supposée précédemment. SAGA est évolutivement bien conservée, de la levure aux mammifères, et possède une fonction d’histone acétyltransférase (HAT). Chez les métazoaires, l’activité HAT de SAGA est partagée avec un autre complexe, le complexe ATAC. Des nouvelles approches m’ont permis de montrer qu’ATAC et SAGA ont des rôles cruciaux pour la maintenance de la pluripotence des cellules souches embryonnaires de souris. Des analyses d’ARN nouvellement-synthétises ont démontré que l’inactivation des complexes ATAC et SAGA modifient l’expression de groupes de gènes différents et aboutent à des phénotypes relativement différents dans ces cellules. Enfin, j’ai pu montrer que les anomalies transcriptionnelles et les phénotypes observé ne semble pas liées à l’activité HAT partagée entre ces deux complexes. Par conséquent, nos données indiquent que les complexes ATAC et SAGA ont des rôles importants et indépendants du HAT dans les cellules mammifères.</dcterms:abstract>
<dcterms:abstract xml:lang="en">Recent studies from my host laboratory indicate that the histone modifying complex SAGA acts as a general cofactor for RNA polymerase II transcription in budding yeast in contrast to its previously assumed specific functions. SAGA is evolutionarily well conserved, from yeast to mammals, and has a histone acetyltransferase (HAT) function. In metazoans, the HAT activity of SAGA is shared with another complex, the ATAC complex. New approaches have allowed me to demonstrate that SAGA and ATAC have crucial roles in maintaining stemness of mouse embryonic stem cells. Newly synthesized RNA analyses revealed that inactivation of the SAGA and ATAC complexes influences the expression of different groups of genes and results in relatively distinct phenotypes in these cells. Finally, I was able to show that the transcriptional anomalies and the observed phenotypes do not seem to be linked to the HAT activity shared by these two complexes. Therefore, our data indicate that SAGA and ATAC have important, HAT-independent roles in mammalian cells.</dcterms:abstract>
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