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转录因子 Grainyhead-like 2 调节上皮顶端连接复合体的分子组成。

The transcription factor grainyhead-like 2 regulates the molecular composition of the epithelial apical junctional complex.

机构信息

Max-Delbrück Center for Molecular Medicine, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.

出版信息

Development. 2010 Nov;137(22):3835-45. doi: 10.1242/dev.055483.

Abstract

Differentiation of epithelial cells and morphogenesis of epithelial tubes or layers is closely linked with the establishment and remodeling of the apical junctional complex, which includes adherens junctions and tight junctions. Little is known about the transcriptional control of apical junctional complex components. Here, we show that the transcription factor grainyhead-like 2 (Grhl2), an epithelium-specific mammalian homolog of Drosophila Grainyhead, is essential for adequate expression of the adherens junction gene E-cadherin and the tight junction gene claudin 4 (Cldn4) in several types of epithelia, including gut endoderm, surface ectoderm and otic epithelium. We have generated Grhl2 mutant mice to demonstrate defective molecular composition of the apical junctional complex in these compartments that coincides with the occurrence of anterior and posterior neural tube defects. Mechanistically, we show that Grhl2 specifically associates with cis-regulatory elements localized at the Cldn4 core promoter and within intron 2 of the E-cadherin gene. Cldn4 promoter activity in epithelial cells is crucially dependent on the availability of Grhl2 and on the integrity of the Grhl2-associated cis-regulatory element. At the E-cadherin locus, the intronic Grhl2-associated cis-regulatory region contacts the promoter via chromatin looping, while loss of Grhl2 leads to a specific decrease of activating histone marks at the E-cadherin promoter. Together, our data provide evidence that Grhl2 acts as a target gene-associated transcriptional activator of apical junctional complex components and, thereby, crucially participates in epithelial differentiation.

摘要

上皮细胞的分化和上皮管或层的形态发生与顶端连接复合体的建立和重塑密切相关,顶端连接复合体包括黏附连接和紧密连接。关于顶端连接复合体成分的转录控制知之甚少。在这里,我们表明,转录因子颗粒头样 2(Grhl2)是果蝇颗粒头样的哺乳动物同源物,是几种上皮细胞(包括肠道内胚层、表面外胚层和耳上皮)中黏附连接基因 E-钙黏蛋白和紧密连接基因 claudin 4(Cldn4)充分表达所必需的。我们已经生成了 Grhl2 突变小鼠,以证明这些隔室中顶端连接复合体的分子组成存在缺陷,这与前神经管和后神经管缺陷的发生相一致。从机制上讲,我们表明 Grhl2 特异性地与位于 Cldn4 核心启动子内和 E-钙黏蛋白基因内含子 2 内的顺式调节元件结合。上皮细胞中 Cldn4 启动子活性的关键取决于 Grhl2 的可用性和 Grhl2 相关顺式调节元件的完整性。在 E-钙黏蛋白基因座上,内含子中的 Grhl2 相关顺式调节区通过染色质环化与启动子接触,而 Grhl2 的缺失导致 E-钙黏蛋白启动子上激活组蛋白标记的特异性减少。总之,我们的数据提供了证据表明,Grhl2 作为靶基因相关转录激活剂发挥作用,是顶端连接复合体成分的关键参与者,并因此参与上皮细胞分化。

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