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Spi-1/PU.1和Spi-B转录因子的DNA结合特异性以及c-fes/c-fps启动子中Spi-1/Spi-B结合位点的鉴定。

DNA binding specificities of Spi-1/PU.1 and Spi-B transcription factors and identification of a Spi-1/Spi-B binding site in the c-fes/c-fps promoter.

作者信息

Ray-Gallet D, Mao C, Tavitian A, Moreau-Gachelin F

机构信息

Unité 248 INSERM, Faculté de Médecine Lariboisière Saint-Louis, Paris, France.

出版信息

Oncogene. 1995 Jul 20;11(2):303-13.

PMID:7624145
Abstract

Spi-1/PU.1 and Spi-B encode hematopoietic-specific transcription factors that are the most distantly related members of the Ets family. The Ets proteins share a conserved 85 amino acids DNA binding domain, the Ets domain and recognize various DNA target sites around a common core 5'-GGAA/T-3'. The DNA binding specificities of Spi-1 and Spi-B were investigated by using the method of polymerase chain reaction (PCR)-mediated random site selection. The deduced Spi-1 and Spi-B consensus binding sites are very similar suggesting that the functional activities of Spi-1 and Spi-B cannot be distinguished on the basis of their DNA binding specificities. We identified a putative Spi-1/Spi-B binding site in the promoter region of the c-fes/c-fps protooncogene which encodes a tyrosine kinase expressed predominantly in myeloid cells. In vitro translated Spi-1 and Spi-B proteins were capable to bind this site similarly and to activate the c-fes promoter in HeLa transfected cells. We showed that Spi-1 binds the Spi-1/Spi-B binding site of c-fes in HL-60 cells suggesting that Spi-1 may be involved in the regulation of c-fes transcription in myeloid cells. Intriguingly, we detected only Spi-1 binding to this site in the Raji cell line which express both Spi-1 and Spi-B proteins. This suggests that Spi-1 and Spi-B exhibit different DNA binding activities in vivo although they share similar DNA binding specificities in vitro.

摘要

Spi-1/PU.1和Spi-B编码造血特异性转录因子,它们是Ets家族中亲缘关系最远的成员。Ets蛋白共享一个由85个氨基酸组成的保守DNA结合结构域,即Ets结构域,并识别围绕共同核心序列5'-GGAA/T-3'的各种DNA靶位点。通过聚合酶链反应(PCR)介导的随机位点选择方法研究了Spi-1和Spi-B的DNA结合特异性。推导的Spi-1和Spi-B共有结合位点非常相似,这表明不能根据它们的DNA结合特异性来区分Spi-1和Spi-B的功能活性。我们在c-fes/c-fps原癌基因的启动子区域鉴定了一个假定的Spi-1/Spi-B结合位点,该基因编码一种主要在髓样细胞中表达的酪氨酸激酶。体外翻译的Spi-1和Spi-B蛋白能够类似地结合该位点,并在转染HeLa细胞中激活c-fes启动子。我们发现Spi-1在HL-60细胞中结合c-fes的Spi-1/Spi-B结合位点,这表明Spi-1可能参与髓样细胞中c-fes转录的调控。有趣的是,我们在同时表达Spi-1和Spi-B蛋白的Raji细胞系中仅检测到Spi-1与该位点结合。这表明Spi-1和Spi-B在体内表现出不同的DNA结合活性,尽管它们在体外具有相似的DNA结合特异性。

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