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髓样锌指蛋白 1 和 GA 结合蛋白在调节癌细胞中 Yes 相关蛋白 1 的表达中与 Sox2 协同作用。

Myeloid Zinc Finger 1 and GA Binding Protein Co-Operate with Sox2 in Regulating the Expression of Yes-Associated Protein 1 in Cancer Cells.

机构信息

Department of Microbiology, NYU School of Medicine, New York, New York, USA.

出版信息

Stem Cells. 2017 Dec;35(12):2340-2350. doi: 10.1002/stem.2705. Epub 2017 Sep 29.

Abstract

The transcription factor (TF) yes-associated protein 1 (YAP1) is a major effector of the tumor suppressive Hippo signaling pathway and is also necessary to maintain pluripotency in embryonic stem cells. Elevated levels of YAP1 expression antagonize the tumor suppressive effects of the Hippo pathway that normally represses YAP1 function. High YAP1 expression is observed in several types of human cancers and is particularly prominent in cancer stem cells (CSCs). The stem cell TF Sox2, which marks and maintains CSCs in osteosarcomas (OSs), promotes YAP1 expression by binding to an intronic enhancer element and YAP1 expression is also crucial for the maintainance of OS stem cells. To further understand the regulation of YAP1 expression in OSs, we subjected the YAP1 intronic enhancer to scanning mutagenesis to identify all DNA cis-elements critical for enhancer function. Through this approach, we identified two novel TFs, GA binding protein (GABP) and myeloid zinc finger 1 (MZF1), which are essential for basal YAP1 transcription. These factors are highly expressed in OSs and bind to distinct sites in the YAP1 enhancer. Depletion of either factor leads to drastically reduced YAP1 expression and thus a reversal of stem cell properties. We also found that YAP1 can regulate the expression of Sox2 by binding to two distinct DNA binding sites upstream and downstream of the Sox2 gene. Thus, Sox2 and YAP1 reinforce each others expression to maintain stemness and tumorigenicity in OSs, but the activity of MZF1 and GABP is essential for YAP1 transcription. Stem Cells 2017;35:2340-2350.

摘要

转录因子(TF)Yes 相关蛋白 1(YAP1)是肿瘤抑制 Hippo 信号通路的主要效应因子,也是维持胚胎干细胞多能性所必需的。YAP1 表达水平的升高拮抗了 Hippo 通路的肿瘤抑制作用,而 Hippo 通路通常会抑制 YAP1 功能。在几种类型的人类癌症中观察到高 YAP1 表达,并且在癌症干细胞(CSC)中尤为突出。干细胞 TF Sox2 标记并维持骨肉瘤(OS)中的 CSCs,通过结合内含子增强子元件促进 YAP1 表达,YAP1 表达对于维持 OS 干细胞也是至关重要的。为了进一步了解 OS 中 YAP1 表达的调控,我们对 YAP1 内含子增强子进行扫描诱变,以鉴定所有对增强子功能至关重要的 DNA 顺式元件。通过这种方法,我们鉴定了两个新的 TF,GA 结合蛋白(GABP)和髓样锌指 1(MZF1),它们是基础 YAP1 转录所必需的。这些因子在 OS 中高度表达,并结合在 YAP1 增强子的不同位点上。任一因子的耗竭都会导致 YAP1 表达急剧减少,从而逆转干细胞特性。我们还发现 YAP1 可以通过结合 Sox2 基因上下游的两个不同 DNA 结合位点来调节 Sox2 的表达。因此,Sox2 和 YAP1 通过相互增强彼此的表达来维持 OS 中的干细胞特性和致瘤性,但 MZF1 和 GABP 的活性对于 YAP1 转录是必需的。《干细胞》2017 年;35:2340-2350。

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