Ma X P, Calabretta B
Jefferson Cancer Institute, Thomas Jefferson University, Philadelphia, Pennsylvania 19107.
Cancer Res. 1994 Dec 15;54(24):6512-6.
A partial-length A-myb complementary DNA recently cloned by low-stringency hybridization with a c-myb probe to complementary DNA libraries derived from human cell lines showed a high degree of homology with the DNA-binding domain of c-myb and B-myb, suggesting that A-myb also encoded a DNA-binding protein. We report here the sequence of the entire coding region of A-myb complementary DNA and show that the full-length GST-A-myb fusion protein or a truncated derivative corresponding only to the putative DNA-binding domain interacts specifically with Myb-binding sites of the c-myb responsive promoters, MIM-1 and CD34. In transient transfection assays, A-myb transactivated the bound promoters. These results suggest that, analogous to the other members of the Myb family, the A-myb gene encodes a bona fide transactivator. The distinct function of A-myb might derive from its pattern of expression and/or its relative potency as a transactivator of myb target genes.
最近通过用c-myb探针与来源于人细胞系的互补DNA文库进行低严格度杂交克隆出的部分长度A-myb互补DNA,显示出与c-myb和B-myb的DNA结合结构域高度同源,这表明A-myb也编码一种DNA结合蛋白。我们在此报告A-myb互补DNA整个编码区的序列,并表明全长GST-A-myb融合蛋白或仅对应于推定DNA结合结构域的截短衍生物与c-myb反应性启动子MIM-1和CD34的Myb结合位点特异性相互作用。在瞬时转染实验中,A-myb激活了结合的启动子。这些结果表明,与Myb家族的其他成员类似,A-myb基因编码一种真正的反式激活因子。A-myb的独特功能可能源于其表达模式和/或其作为myb靶基因反式激活因子的相对效力。