Tbx20 dose-dependently regulates transcription factor networks required for mouse heart and motoneuron development

Tbx20 dose-dependently regulates transcription factor networks required for mouse heart and motoneuron development

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dc.contributor.author Bruneau, Benoit G.
dc.contributor.author Nagy, Andras
dc.contributor.author Mo, Rong
dc.contributor.author Nemer, Mona
dc.contributor.author Black, Brian L.
dc.contributor.author Hui, Chi-chung
dc.contributor.author Henkelman, Mark
dc.contributor.author Davidson, Lorinda
dc.contributor.author Georges, Romain
dc.contributor.author Gertsenstein, Marina
dc.contributor.author Heidt, Analeah B.
dc.contributor.author Mori, Alessandro D.
dc.contributor.author Mileikovskaia, Maria
dc.contributor.author Koshiba-Takeuchi, Kazuko
dc.contributor.author Arruda, Eric P.
dc.contributor.author Takeuchi, Jun K
dc.date.accessioned 2010-01-28T14:16:02Z
dc.date.available 2010-01-28T14:16:02Z
dc.date.created 2005
dc.date.issued 2010-01-28T14:16:02Z
dc.identifier doi:10.1242/dev.01827
dc.identifier.citation Development, 132(10), 2463-2474 en
dc.identifier.uri http://hdl.handle.net/10393/12782
dc.description.abstract To elucidate the function of the T-box transcription factor Tbx20 in mammalian development, we generated a graded loss-of-function series by transgenic RNA interference in entirely embryonic stem cell-derived mouse embryos. Complete Tbx20 knockdown resulted in defects in heart formation, including hypoplasia of the outflow tract and right ventricle, which derive from the anterior heart field (AHF), and decreased expression of Nkx2-5 and Mef2c, transcription factors required for AHF formation. A mild knockdown led to persistent truncus arteriosus (unseptated outflow tract) and hypoplastic right ventricle, entities similar to human congenital heart defects, and demonstrated a critical requirement for Tbx20 in valve formation. Finally, an intermediate knockdown revealed a role for Tbx20 in motoneuron development, specifically in the regulation of the transcription factors Isl2 and Hb9, which are important for terminal differentiation of motoneurons. Tbx20 could activate promoters/enhancers of several genes in cultured cells, including the Mef2c AHF enhancer and the Nkx2-5 cardiac enhancer. The Mef2c AHF enhancer relies on Isl1- and Gata-binding sites. We identified a similar Isl1 binding site in the Nkx2-5 AHF enhancer, which in transgenic mouse embryos was essential for activity in a large part of the heart, including the outflow tract. Tbx20 synergized with Isl1 and Gata4 to activate both the Mef2c and Nkx2-5 enhancers, thus providing a unifying mechanism for gene activation by Tbx20 in the AHF. We conclude that Tbx20 is positioned at a critical node in transcription factor networks required for heart and motoneuron development where it dose-dependently regulates gene expression. en
dc.language.iso en en
dc.subject Mouse en
dc.subject Transcription factors en
dc.subject T-box en
dc.subject Tbx20 en
dc.subject Heart en
dc.subject RNAi en
dc.subject Optical projection tomography en
dc.subject Embryo en
dc.subject Motoneurons en
dc.title Tbx20 dose-dependently regulates transcription factor networks required for mouse heart and motoneuron development en
dc.type Article en

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