Rambaldi I, Kovàcs E N, Featherstone M S
McGill Cancer Centre, Montréal, Québec, Canada.
Nucleic Acids Res. 1994 Feb 11;22(3):376-82. doi: 10.1093/nar/22.3.376.
The product of the murine Hoxd-4 (Hox-4.2) gene is a transcription factor that acts upon an autoregulatory element in Hoxd-4 upstream sequences (1). Using this activity as an assay in transient transfections of P19 embryonal carcinoma (EC) cells, we performed a mutational analysis to map functional domains in the HOXD-4 protein. The importance of the homeodomain was shown by a single amino acid change in this region that abolished activity. Deletion analysis revealed that many evolutionarily conserved regions outside of the homeodomain were dispensable for activation in our assay. Fusions to the GAL4 DNA-binding domain mapped a transcriptional activation function to the HOXD-4 proline-rich N-terminus. The proline-rich transcription factor AP2 squelched activation by HOXD-4 and by GAL4/HOXD-4 N-terminus fusion proteins. Together, these results suggest that HOXD-4 harbors a transcriptional activation domain of the proline-rich type.
小鼠Hoxd-4(Hox-4.2)基因的产物是一种转录因子,它作用于Hoxd-4上游序列中的一个自调控元件(1)。利用这种活性作为P19胚胎癌细胞瞬时转染的一种检测方法,我们进行了突变分析,以定位HOXD-4蛋白中的功能结构域。同源结构域中一个氨基酸的改变消除了活性,这表明了同源结构域的重要性。缺失分析显示,在我们的检测中,同源结构域外许多进化上保守的区域对于激活是可有可无的。与GAL4 DNA结合结构域的融合将转录激活功能定位到HOXD-4富含脯氨酸的N末端。富含脯氨酸的转录因子AP2抑制了HOXD-4以及GAL4/HOXD-4 N末端融合蛋白的激活作用。这些结果共同表明,HOXD-4含有一个富含脯氨酸类型的转录激活结构域。