Margalit Y, Yarus S, Shapira E, Gruenbaum Y, Fainsod A
Department of Cellular Biochemistry, Hebrew University-Hadassah Medical School, Jerusalem, Israel.
Nucleic Acids Res. 1993 Oct 25;21(21):4915-22. doi: 10.1093/nar/21.21.4915.
The DNA binding specificity of the chicken homeodomain protein CDXA was studied. Using a CDXA-glutathione-S-transferase fusion protein, DNA fragments containing the binding site for this protein were isolated. The sources of DNA were oligonucleotides with random sequence and chicken genomic DNA. The DNA fragments isolated were sequenced and tested in DNA binding assays. Sequencing revealed that most DNA fragments are AT rich which is a common feature of homeodomain binding sites. By electrophoretic mobility shift assays it was shown that the different target sequences isolated bind to the CDXA protein with different affinities. The specific sequences bound by the CDXA protein in the genomic fragments isolated, were determined by DNase I footprinting. From the footprinted sequences, the CDXA consensus binding site was determined. The CDXA protein binds the consensus sequence A, A/T, T, A/T, A, T, A/G. The CAUDAL binding site in the ftz promoter is also included in this consensus sequence. When tested, some of the genomic target sequences were capable of enhancing the transcriptional activity of reporter plasmids when introduced into CDXA expressing cells. This study determined the DNA sequence specificity of the CDXA protein and it also shows that this protein can further activate transcription in cells in culture.
对鸡同源结构域蛋白CDXA的DNA结合特异性进行了研究。利用CDXA-谷胱甘肽-S-转移酶融合蛋白,分离出含有该蛋白结合位点的DNA片段。DNA的来源是随机序列的寡核苷酸和鸡基因组DNA。对分离出的DNA片段进行测序,并在DNA结合试验中进行检测。测序显示,大多数DNA片段富含AT,这是同源结构域结合位点的一个共同特征。通过电泳迁移率变动分析表明,分离出的不同靶序列以不同亲和力与CDXA蛋白结合。通过DNase I足迹法确定了分离的基因组片段中CDXA蛋白结合的特定序列。从足迹序列中确定了CDXA共有结合位点。CDXA蛋白结合共有序列A、A/T、T、A/T、A、T、A/G。ftz启动子中的尾型结合位点也包含在该共有序列中。经测试,一些基因组靶序列在导入表达CDXA的细胞时能够增强报告质粒的转录活性。这项研究确定了CDXA蛋白的DNA序列特异性,并且还表明该蛋白可以在培养细胞中进一步激活转录。