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触角足蛋白P2启动子的体外分析:一种新型果蝇转录因子的鉴定

In vitro analysis of the Antennapedia P2 promoter: identification of a new Drosophila transcription factor.

作者信息

Perkins K K, Dailey G M, Tjian R

机构信息

Howard Hughes Medical Institute, Department of Biochemistry, University of California, Berkeley 94720.

出版信息

Genes Dev. 1988 Dec;2(12A):1615-26. doi: 10.1101/gad.2.12a.1615.

Abstract

We have investigated the transcriptional regulation of the Antennapedia P2 (Antp P2) promoter using nuclear extracts prepared from Drosophila embryos. Transcriptional analysis of deletion mutants reveals the presence of multiple cis-regulatory elements located both upstream and downstream of the start site. One of the elements appears to mediate negative regulation, since deletion of this element results in higher levels of transcription. Several factors that interact with these control elements have been detected and isolated. One DNA-binding protein, Drosophila Transcription Factor-1 (DTF-1), specifically recognizes the consensus sequence GCAACAT/CG/C that is reiterated four times within an upstream activating element. DTF-1 was purified by sequence-specific DNA affinity chromatography and identified as a doublet of approximately 50 kD. Purified DTF-1 enhances transcription from the Antp P2 promoter 7- to 15-fold in a binding site-dependent manner.

摘要

我们使用从果蝇胚胎制备的核提取物研究了触角足P2(Antp P2)启动子的转录调控。缺失突变体的转录分析揭示了位于起始位点上游和下游的多个顺式调控元件的存在。其中一个元件似乎介导负调控,因为缺失该元件会导致更高水平的转录。已经检测并分离出了几种与这些控制元件相互作用的因子。一种DNA结合蛋白,果蝇转录因子-1(DTF-1),特异性识别共有序列GCAACAT/CG/C,该序列在上游激活元件中重复出现四次。DTF-1通过序列特异性DNA亲和色谱法纯化,并被鉴定为约50 kD的双峰。纯化的DTF-1以结合位点依赖的方式将Antp P2启动子的转录增强7至15倍。

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