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C-terminal-binding protein corepresses epithelial and proapoptotic gene expression programs.

机译:C末端结合蛋白可上皮和促凋亡基因表达程序。

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The genesis of carcinoma cells often involves epithelial-to-mesenchymal transitions and the acquisition of apoptosis resistance, but it is unclear whether these alterations are controlled coordinately or independently. Our previously reported effects of adenovirus E1a in human tumor cells raised the possibility that the E1a-interacting corepressor protein C-terminal-binding protein (CtBP) might selectively repress epithelial cell adhesion and proapoptotic genes. Here, we report that CtBP-knockout cells were hypersensitive to apoptosis. Correspondingly, microarray analysis of CtBP-knockout vs. CtBP-rescued mouse embryo fibroblasts revealed that many epithelial-specific and proapoptotic genes were indeed regulated by CtBP. Neither the apoptosis nor the repression activities of CtBP required histidine-315, suggesting that the proposed dehydrogenase activity is not essential for CtBP function. The results presented herein establish two functional roles of CtBP: to corepress epithelial genes, thus permitting epithelial-to-mesenchymal transitions, and to modulate the cellular threshold for apoptotic responses.
机译:癌细胞的发生通常涉及上皮到间充质的转变和凋亡抗性的获得,但是尚不清楚这些改变是协同控制还是独立控制。我们先前报道的腺病毒E1a在人肿瘤细胞中的作用增加了这种可能性,即与E1a相互作用的核心加压蛋白C末端结合蛋白(CtBP)可能选择性抑制上皮细胞粘附和促凋亡基因。在这里,我们报道CtBP基因敲除细胞对凋亡高度敏感。相应地,CtBP基因敲除与CtBP拯救的小鼠胚胎成纤维细胞的微阵列分析显示,许多上皮特异性基因和促凋亡基因确实受CtBP调控。 CtBP的凋亡或抑制活性均不需要组氨酸315,这表明拟议的脱氢酶活性对于CtBP的功能不是必需的。本文介绍的结果建立了CtBP的两个功能作用:共压上皮基因,从而允许上皮到间充质的转换,以及调节细胞凋亡阈值。

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