Chatton B, Bahr A, Acker J, Kedinger C
LGME/CNRS, Strasbourg, France.
Biotechniques. 1995 Jan;18(1):142-5.
We describe a multipurpose eukaryotic expression vector that incorporates the following features: restriction sites for in-frame insertion of cDNAs of interest between sequences encoding the glutathione-S-transferase (GST) and an oligohistidine element, allowing expression of the corresponding fusion proteins; a phosphorylation site for protein kinase A for in vitro labeling of the fusion protein; a T7 promoter for in vitro transcription and subsequent translation; and signals for single-stranded DNA production in bacteria. We have used this vector to demonstrate the formation in vivo of complexes between the transcription factor ATFa, a member of the family of ATF/CRE binding proteins, and the c-Jun or c-Fos proteins. Such interactions could be detected in crude extracts from cells transfected with vectors expressing the GST-ATFa fusion protein, as well as the c-Jun or c-Fos proteins. Complexes containing both ATFa and either c-Jun or c-Fos were specifically retained on glutathione (GSH)-agarose beads as revealed by immunoblot analyses. We also show that the leucine zipper domain of ATFa is essential for this interaction.
我们描述了一种多功能真核表达载体,其具有以下特征:在编码谷胱甘肽-S-转移酶(GST)和寡聚组氨酸元件的序列之间存在用于框内插入感兴趣的cDNA的限制性酶切位点,从而允许表达相应的融合蛋白;具有蛋白激酶A的磷酸化位点,用于融合蛋白的体外标记;具有T7启动子,用于体外转录和随后的翻译;以及在细菌中产生单链DNA的信号。我们使用该载体证明了转录因子ATFa(ATF/CRE结合蛋白家族的成员)与c-Jun或c-Fos蛋白在体内形成复合物。在用表达GST-ATFa融合蛋白以及c-Jun或c-Fos蛋白的载体转染的细胞的粗提物中可以检测到这种相互作用。免疫印迹分析表明,含有ATFa和c-Jun或c-Fos的复合物特异性保留在谷胱甘肽(GSH)琼脂糖珠上。我们还表明,ATFa的亮氨酸拉链结构域对于这种相互作用至关重要。