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Identification and characterization of a cis-acting element that interferes with glucocorticoid-inducible activation of the mouse mammary tumor virus promoter.

机译:干扰小鼠糖皮质激素诱导的小鼠乳腺肿瘤病毒启动子激活的顺式作用元件的鉴定和表征。

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摘要

The rat hepatoma cell line M1.19 is stably infected by the mouse mammary tumor virus (MMTV), and the expression of the virus is induced by glucocorticoid treatment. However, in the 6.10.2 variant of M1.19, an increase in MMTV transcription is hardly detectable upon exposure to hormone. The mechanism of hormone-unresponsiveness in these cells has been unclear. In this study, we show that nuclear extract from 6.10.2 cells contains a specific DNA-binding activity that recognizes a sequence motif extending from positions -163 to -147 on the MMTV promoter. An oligonucleotide probe spanning this region binds a nuclear factor distinct from the glucocorticoid receptor. In vivo competition experiments, where increased amounts of a plasmid containing this element were transfected into 6.10.2 cells, showed a dose-dependent increase in hormonal inducibility of MMTV expression. Together, these results indicate that this sequence motif negatively modulates glucocorticoid-inducible activation of the MMTV promoter. Moreover, we have characterized a nuclear factor that preferentially binds to the coding strand of this element.
机译:大鼠肝癌细胞系M1.19被小鼠乳腺肿瘤病毒(MMTV)稳定感染,并且该病毒的表达通过糖皮质激素治疗诱导。但是,在M1.19的6.10.2变体中,暴露于激素后几乎无法检测到MMTV转录的增加。这些细胞中激素无反应性的机制尚不清楚。在这项研究中,我们表明,来自6.10.2细胞的核提取物包含特定的DNA结合活性,该活性识别MMTV启动子上从位置-163到-147的序列基序。跨越该区域的寡核苷酸探针结合不同于糖皮质激素受体的核因子。在体内竞争实验中,将增加量的含有该元素的质粒转染到6.10.2细胞中,结果表明MMTV表达的激素诱导能力呈剂量依赖性增加。总之,这些结果表明该序列基序负调节了MMTV启动子的糖皮质激素诱导的激活。此外,我们已经表征了优先结合该元件编码链的核因子。

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