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Sp和螺旋-环-螺旋转录因子在人类Id4基因启动子活性调控中的作用。

A role for Sp and helix-loop-helix transcription factors in the regulation of the human Id4 gene promoter activity.

作者信息

Pagliuca A, Cannada-Bartoli P, Lania L

机构信息

Department of Genetics, Molecular and General Biology, University of Naples "Federico II," via Mezzocannone 8, 80134 Naples, Italy.

出版信息

J Biol Chem. 1998 Mar 27;273(13):7668-74. doi: 10.1074/jbc.273.13.7668.

Abstract

Id family helix-loop-helix (HLH) proteins are involved in the regulation of proliferation and differentiation of several cell types. To identify cis- and trans-acting factors that regulate Id4 gene expression, we have analyzed the promoter regulatory sequences of the human Id4 gene in transient transfections and gel mobility shift assays. We have identified two functional elements, both located downstream from the TATA motif, that control Id4 promoter activity. One element contains a consensus E-box, and we demonstrated that the protein complex binding to the E-box contains the bHLH-zip upstream stimulatory factor (USF) transcription factor. Enforced expression of USF1 leads to E-box-mediated stimulation of promoter activity. The E-box also mediated stimulatory effects of several bHLH transcription factors, and co-expression of Id4 blocked the stimulatory effect mediated by the bHLH factors. A second element is a GA motif, located downstream from the transcriptional start sites, mutation of which resulted in a 20-fold increase in transcriptional activity. Gel-shift analysis and transfections into Drosophila Schneider SL2 cells showed that the repressor element is recognized by both Sp1 and Sp3 factors. These data suggest that Id4 transcription control is highly complex, involving both negative and positive regulatory elements, including a novel inhibitory function exerted by Sp1 and Sp3 transcription factors.

摘要

Id家族螺旋-环-螺旋(HLH)蛋白参与多种细胞类型的增殖和分化调控。为了鉴定调控Id4基因表达的顺式和反式作用因子,我们在瞬时转染和凝胶迁移率变动分析中分析了人类Id4基因的启动子调控序列。我们鉴定出两个功能元件,均位于TATA基序下游,它们控制Id4启动子活性。一个元件包含一个共有E盒,并且我们证明与E盒结合的蛋白复合物包含bHLH-zip上游刺激因子(USF)转录因子。USF1的强制表达导致E盒介导的启动子活性刺激。E盒也介导了几种bHLH转录因子的刺激作用,并且Id4的共表达阻断了bHLH因子介导的刺激作用。第二个元件是一个GA基序,位于转录起始位点下游,其突变导致转录活性增加20倍。凝胶迁移分析和转染到果蝇Schneider SL2细胞中表明,阻遏元件被Sp1和Sp3因子识别。这些数据表明,Id4转录调控非常复杂,涉及正负调控元件,包括Sp1和Sp3转录因子发挥的一种新的抑制功能。

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