核因子与c-myc基因上游区域的结合。

Oncogene research Pub Date : 1991-01-01
K Saksela, P J Koskinen, K Alitalo
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引用次数: 0

摘要

我们研究了蛋白质与人类c-myc基因上游区域21个碱基对序列对应的合成DNA片段的结合。该序列先前已被报道与c-myc蛋白结合,因此代表了c-myc基因自动调节的假定位点(Ariga等人,1989)。我们的电泳迁移转移试验表明,该DNA片段结合到HeLa细胞核提取物中存在的一个因子。然而,对其他细胞提取物的分析表明,这种结合与c-myc蛋白的存在无关。体外翻译的c-myc蛋白未观察到结合。此外,抗c-myc抗体不能抑制该因子的结合。这些实验表明,来自c-myc基因P1启动子的核苷酸-2193到-2173能够结合一个核因子,而这个核因子很可能不包括c-myc蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Binding of a nuclear factor to the upstream region of the c-myc gene.

We have studied the binding of proteins to a synthetic DNA fragment corresponding to a 21 base pair sequence in the upstream region of the human c-myc gene. This sequence has previously been reported to bind the c-myc protein, thus representing a putative site for autoregulation of the c-myc gene (Ariga et al., 1989). Our electrophoretic mobility shift assays indicated that this DNA fragment binds to a factor present in nuclear extracts from HeLa cells. However, analysis of extracts from other cells indicated that this binding does not correlate with the presence of the c-myc protein. No binding was observed using c-myc protein translated in vitro. Also, anti-c-myc antibodies could not inhibit binding of this factor. These experiments indicate, that nucleotides -2193 to -2173 from the P1 promoter of the c-myc gene are able to bind a nuclear factor, and that this factor most likely does not include the c-myc protein.

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