Klempnauer K H
Hans-Spemann-Laboratory, Max-Planck-Institute for Immunobiology, Freiburg, Germany.
Oncogene. 1993 Jan;8(1):111-5.
The retroviral oncogene v-myb and its cellular homolog c-myb encode nuclear DNA-binding phosphoproteins (v-MYB and c-MYB) that function as transcriptional regulators. v-MYB and c-MYB recognize a nucleotide sequence motif, PyAACG/TG, that is present in the promoter region of the myb-inducible mim-1 gene and is required for regulation of mim-1 expression by v-MYB and c-MYB. Since the myb-binding motif contains a CpG dinucleotide that constitutes a potential target for methylation, we have investigated whether recognition of the binding site by myb proteins is sensitive to CpG methylation of the binding motif. The results presented here demonstrate that bacterially expressed v-MYB as well as authentic v-MYB and c-MYB bind to the myb binding site in a methylation-sensitive manner. Our observations raise the interesting possibility that myb function can be regulated by methylation of myb binding sites.
逆转录病毒癌基因v-myb及其细胞同源物c-myb编码核DNA结合磷蛋白(v-MYB和c-MYB),它们作为转录调节因子发挥作用。v-MYB和c-MYB识别一个核苷酸序列基序PyAACG/TG,该基序存在于myb诱导的mim-1基因的启动子区域,是v-MYB和c-MYB调节mim-1表达所必需的。由于myb结合基序包含一个构成潜在甲基化靶点的CpG二核苷酸,我们研究了myb蛋白对结合位点的识别是否对结合基序的CpG甲基化敏感。此处给出的结果表明,细菌表达的v-MYB以及天然的v-MYB和c-MYB以甲基化敏感的方式结合到myb结合位点。我们的观察结果提出了一个有趣的可能性,即myb功能可以通过myb结合位点的甲基化来调节。