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Myc与β-连环蛋白协同作用,驱动肾单位祖细胞中的基因表达。

Myc cooperates with β-catenin to drive gene expression in nephron progenitor cells.

作者信息

Pan Xinchao, Karner Courtney M, Carroll Thomas J

机构信息

Department of Internal Medicine (Nephrology), UT Southwestern Medical Center, Dallas, TX 75390-9148, USA.

Molecular Biology, UT Southwestern Medical Center, Dallas, TX 75390-9148, USA.

出版信息

Development. 2017 Nov 15;144(22):4173-4182. doi: 10.1242/dev.153700. Epub 2017 Oct 9.

Abstract

For organs to achieve their proper size, the processes of stem cell renewal and differentiation must be tightly regulated. We previously showed that in the developing kidney, Wnt9b regulates distinct β-catenin-dependent transcriptional programs in the renewing and differentiating populations of the nephron progenitor cells. How β-catenin stimulated these two distinct programs was unclear. Here, we show that β-catenin cooperates with the transcription factor Myc to activate the progenitor renewal program. Although in multiple contexts Myc is a target of β-catenin, our characterization of a cell type-specific enhancer for the Wnt9b/β-catenin target gene shows that Myc and β-catenin cooperate to activate gene expression controlled by this element. This appears to be a more general phenomenon as we find that Myc is required for the expression of every Wnt9b/β-catenin progenitor renewal target assessed as well as for proper nephron endowment This study suggests that, within the developing kidney, tissue-specific β-catenin activity is regulated by cooperation with cell type-specific transcription factors. This finding not only provides insight into the regulation of β-catenin target genes in the developing kidney, but will also advance our understanding of progenitor cell renewal in other cell types/organ systems in which Myc and β-catenin are co-expressed.

摘要

为使器官发育至正常大小,干细胞的自我更新和分化过程必须受到严格调控。我们先前发现,在发育中的肾脏里,Wnt9b在肾祖细胞的自我更新和分化群体中调控不同的β-连环蛋白依赖性转录程序。β-连环蛋白如何刺激这两个不同的程序尚不清楚。在此,我们表明β-连环蛋白与转录因子Myc协同激活祖细胞自我更新程序。虽然在多种情况下Myc是β-连环蛋白的一个靶点,但我们对Wnt9b/β-连环蛋白靶基因的细胞类型特异性增强子的表征显示,Myc和β-连环蛋白协同激活受该元件控制的基因表达。这似乎是一种更普遍的现象,因为我们发现,对于所评估的每个Wnt9b/β-连环蛋白祖细胞自我更新靶点的表达以及正常的肾单位形成,Myc都是必需的。这项研究表明,在发育中的肾脏内,组织特异性β-连环蛋白活性是通过与细胞类型特异性转录因子协同作用来调控的。这一发现不仅为深入了解发育中肾脏里β-连环蛋白靶基因的调控提供了线索,也将增进我们对其他共表达Myc和β-连环蛋白的细胞类型/器官系统中祖细胞自我更新的理解。

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本文引用的文献

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A synthetic niche for nephron progenitor cells.一种用于肾单位祖细胞的合成微环境。
Dev Cell. 2015 Jul 27;34(2):229-41. doi: 10.1016/j.devcel.2015.06.021. Epub 2015 Jul 16.
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