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首页> 外文期刊>Biochimica et Biophysica Acta. Gene Regulatory Mechanisms >Auto-regulation of Slug mediates its activity during epithelial to mesenchymal transition
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Auto-regulation of Slug mediates its activity during epithelial to mesenchymal transition

机译:Slug的自动调节介导上皮到间质转化过程中的活性

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摘要

Slug, a five C2H2 zinc finger (ZF) motif transcription factor mediates cell migration in development, adult tissue repair and regeneration, as well as during tumor metastases through epithelial to mesenchymal transition. At the molecular level, this involves interactions with E-box (CACC/GGTG) consensus elements within target gene promoters to achieve transcriptional repression. However, precise elucidation of events involved in this DNA recognition and binding of specific promoters to regulate target genes have not been achieved. In the present study, we show that besides transcriptional repression, Slug can also directly activate its own expression by preferential binding to specific E-box elements in the distal binding region of its promoter. Our findings suggest that while the first ZF does not contribute to the transcription-associated functions of Slug, all the remaining four ZFs are involved in regulating the expression of target genes with ZF3 and ZF4 being more crucial than ZF2 or ZF5. We also report that recognition and binding preferences of ZFs are defined through intrinsic differences in the E-box core base pairs and/or flanking sequences, with the S2 E-box element being most critical during autoregulation. However, specific target E-box recognition and binding are also defined by the cellular context, which implies that in silico and/or biochemical DNA binding preferences may not necessarily be able to accurately predict in situ events. Our studies thus constitute a novel understanding of transcriptional regulation. (C) 2015 The Authors. Published by Elsevier B.V.
机译:Slug是一种五种C2H2锌指(ZF)基序转录因子,介导细胞在发育,成年组织修复和再生以及从上皮到间充质的肿瘤转移过程中迁移。在分子水平上,这涉及与靶基因启动子内的E-box(CACC / GGTG)共有元件相互作用,以实现转录抑制。然而,尚未实现对这种DNA识别和特定启动子与调节靶基因结合的事件的精确阐明。在本研究中,我们表明,除了转录抑制作用外,Slug还可以通过优先结合启动子远端结合区域中的特定E-box元件来直接激活其自身表达。我们的发现表明,尽管第一个ZF不能促进Slug的转录相关功能,但其余所有四个ZF都参与调节靶基因的表达,其中ZF3和ZF4比ZF2或ZF5更重要。我们还报告说,ZF的识别和结合偏好是通过E-box核心碱基对和/或侧翼序列中的固有差异定义的,其中S2 E-box元素在自动调节过程中最为关键。但是,特定的靶标E-box识别和结合也由细胞环境来定义,这意味着计算机和/或生化DNA结合偏好可能不一定能够准确地预测原位事件。因此,我们的研究构成了对转录调控的新理解。 (C)2015作者。由Elsevier B.V.发布

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