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COUP-TFII acts downstream of Wnt/β-catenin signal to silence PPARγ gene expression and repress adipogenesis

机译:COUP-TFII在Wnt /β-catenin信号的下游起作用,以沉默PPARγ基因表达并抑制脂肪生成

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摘要

Wnt signaling through β-catenin and TCF maintains preadipocytes in an un-differentiated proliferative state; however, the molecular pathway has not been completely defined. By integrating gene expression microarray, chromatin immunoprecipitation-chip, and cell-based experimental approaches, we show that Wnt/β-catenin signaling activates the expression of COUP-TFII which recruits the SMRT corepressor complex to the first introns located downstream from the first exons of both PPARγ1 and γ2 mRNAs. This maintains the local chromatin in a hypoacetylated state and represses PPARγ gene expression to inhibit adipogenesis. Our experiments define the COUP-TFII/SMRT complex as a previously unappreciated component of the linear pathway that directly links Wnt/β-catenin signaling to repression of PPARγ gene expression and the inhibition of adipogenesis.
机译:通过β-catenin和TCF的Wnt信号转导使前脂肪细胞保持未分化的增殖状态;但是,分子途径尚未完全确定。通过整合基因表达微阵列,染色质免疫沉淀芯片和基于细胞的实验方法,我们表明Wnt /β-catenin信号激活了COUP-TFII的表达,该表达将SMRT corepressor复合体募集到位于第一个外显子下游的第一个内含子PPARγ1和γ2mRNA的表达。这将局部染色质维持在低乙酰化状态,并抑制PPARγ基因表达以抑制脂肪生成。我们的实验将COUP-TFII / SMRT复合物定义为线性通路中以前未曾意识到的组分,该组分直接将Wnt /β-catenin信号传导与PPARγ基因表达的抑制和脂肪形成的抑制联系在一起。

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