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首页> 外文期刊>Molecular and Cellular Biology >SOCS1, SOCS3, and PIAS1 Promote Myogenic Differentiation by Inhibiting the Leukemia Inhibitory Factor-Induced JAK1/STAT1/STAT3 Pathway
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SOCS1, SOCS3, and PIAS1 Promote Myogenic Differentiation by Inhibiting the Leukemia Inhibitory Factor-Induced JAK1/STAT1/STAT3 Pathway

机译:SOCS1,SOCS3和PIAS1通过抑制白血病抑制因子诱导的JAK1 / STAT1 / STAT3途径促进成肌分化。

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摘要

We recently showed that a leukemia inhibitory factor (LIF)-engaged signaling pathway consisting of JAK1, STAT1, and STAT3 plays dual roles in myogenic differentiation: while it participates in myoblast proliferation, it also actively represses differentiation. Downregulation of this pathway is required at the onset of differentiation. However, it remained unclear how this is achieved mechanistically. We now show that SOCS1, SOCS3, and PIAS1 promote myogenic differentiation by specifically inhibiting the LIF-induced JAK1/STAT1/STAT3 pathway via distinct targets; whereas SOCS1 and SOCS3 selectively bind and inhibit JAK1 and gp130, respectively, PIAS1 targets mainly the activated STAT1 and prevents its binding to DNA. We further demonstrated that the SUMO E3-ligase activity of PIAS1 is dispensable for its role in myogenic differentiation. Collectively, our current study revealed a molecular mechanism that explains how the LIF-induced JAK1/STAT1/STAT3 pathway is downregulated upon myogenic differentiation.
机译:我们最近发现,由JAK1,STAT1和STAT3组成的白血病抑制因子(LIF)参与的信号转导通路在成肌分化中起着双重作用:虽然它参与成肌细胞增殖,但也积极抑制分化。在分化开始时需要下调该途径。但是,尚不清楚如何以机械方式实现这一目标。现在,我们显示SOCS1,SOCS3和PIAS1通过特异性抑制LIF诱导的JAK1 / STAT1 / STAT3通路通过不同的靶标来促进成肌分化。而SOCS1和SOCS3分别选择性地结合和抑制JAK1和gp130,PIAS1主要靶向活化的STAT1并阻止其与DNA结合。我们进一步证明了PIAS1的SUMO E3-连接酶活性是必需的,因为它在成肌分化中起着重要的作用。总的来说,我们当前的研究揭示了一种分子机制,该机制解释了LIF诱导的JAK1 / STAT1 / STAT3通路在成肌分化后如何下调。

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