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鉴定调控转化生长因子-β诱导的SNAI1表达的远端增强子

Identification of a Distal Enhancer That Regulates TGF-β-Induced SNAI1 Expression.

作者信息

Fu Hao, Itoh Yuka, Sawaguchi Tomoe, Otake Shigeo, Omata Chiho, Saitoh Masao, Miyazawa Keiji

机构信息

Department of Biochemistry, Graduate School of Medicine, University of Yamanashi, Chuo, Japan.

Research Training Program for Undergraduates, Graduate School of Medicine, University of Yamanashi, Chuo, Japan.

出版信息

Cancer Sci. 2025 May 13. doi: 10.1111/cas.70091.

Abstract

Snail is a zinc finger transcription factor encoded by the SNAI1 gene and triggers a cellular process termed epithelial-mesenchymal transition (EMT) upon its increased expression and/or functional activation. Snail expression and activity are regulated by various extracellular stimuli, including cytokines and environmental factors. Transforming growth factor-β (TGF-β) is a Snail inducer that functions via Smad3-mediated transcriptional activation. In the present study, we identified a distal enhancer that modulates TGF-β-induced SNAI1 expression. ChIP-seq and Hi-C analyses showed that the enhancer is located 46 kb downstream of the SNAI1 gene; in TGF-β-stimulated cells, it associates with Smad3 and interacts with the SNAI1 proximal promoter. Inhibiting the activity of the enhancer using CRISPRi attenuated TGF-β-induced SNAI1 expression, stress fiber formation, and cell motility enhancement, suggesting that the enhancer mediates TGF-β-induced EMT. The enhancer contains a Smad-binding CAGA motif and an activator protein-1 (AP-1) binding motif that function in transcriptional activation. Ras-responsive element binding protein 1 (RREB1), a transcription factor required for TGF-β-induced Snail expression, regulated the basal activity of the enhancer but not its inducibility by TGF-β. In contrast to the enhancer, the association of Smad3 with the proximal promoter was not evident. These findings suggest that the proximal promoter and the distal enhancer respond to distinct signaling cues, integrate them, and cooperatively function to drive SNAI1 expression.

摘要

Snail是一种由SNAI1基因编码的锌指转录因子,当其表达增加和/或功能激活时,会引发一种称为上皮-间质转化(EMT)的细胞过程。Snail的表达和活性受多种细胞外刺激调节,包括细胞因子和环境因素。转化生长因子-β(TGF-β)是一种通过Smad3介导的转录激活发挥作用的Snail诱导剂。在本研究中,我们鉴定了一个调节TGF-β诱导的SNAI1表达的远端增强子。染色质免疫沉淀测序(ChIP-seq)和高通量染色体构象捕获(Hi-C)分析表明,该增强子位于SNAI1基因下游46 kb处;在TGF-β刺激的细胞中,它与Smad3结合并与SNAI1近端启动子相互作用。使用CRISPR干扰抑制增强子的活性可减弱TGF-β诱导的SNAI1表达、应力纤维形成和细胞运动增强,这表明该增强子介导TGF-β诱导的EMT。该增强子包含一个在转录激活中起作用的Smad结合CAGA基序和一个激活蛋白-1(AP-1)结合基序。Ras反应元件结合蛋白1(RREB1)是TGF-β诱导的Snail表达所需的转录因子,它调节增强子的基础活性,但不调节其对TGF-β的诱导性。与增强子不同,Smad3与近端启动子的结合不明显。这些发现表明,近端启动子和远端增强子对不同的信号线索做出反应,整合它们,并协同发挥作用以驱动SNAI1表达。

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