Garcia A, LaMontagne K, Reavis D, Stober-Grässer U, Lipsick J S
Department of Microbiology, School of Medicine, State University of New York, Stony Brook 11794-8621.
Oncogene. 1991 Feb;6(2):265-73.
The v-myb oncogene of the avian myeloblastosis virus encodes a nuclear protein, p48v-myb, which binds to DNA in a sequence-specific manner. We have used wild type and mutant forms of this protein expressed in E. coli to study the protein and DNA determinants for sequence-specific DNA-binding. We have shown that only the highly conserved domain at the amino terminus of p48v-myb is required for sequence-specific DNA-binding. However, neither of the tandem 50 amino acid repeats present in this domain is alone sufficient for such binding. We have also demonstrated that p48v-myb can recognize a single consensus myb binding site and appears to interact with DNA as a protein monomer. In addition, we have shown that sequence-specific binding by p48v-myb requires nucleotides which flank the previously reported PyAACT/GG consensus.
禽成髓细胞瘤病毒的v-myb癌基因编码一种核蛋白p48v-myb,该蛋白以序列特异性方式与DNA结合。我们利用在大肠杆菌中表达的这种蛋白的野生型和突变形式来研究序列特异性DNA结合的蛋白质和DNA决定因素。我们已经表明,p48v-myb氨基末端高度保守的结构域是序列特异性DNA结合所必需的。然而,该结构域中存在的两个串联的50个氨基酸重复序列单独都不足以实现这种结合。我们还证明p48v-myb可以识别单个共有myb结合位点,并且似乎作为蛋白质单体与DNA相互作用。此外,我们已经表明,p48v-myb的序列特异性结合需要位于先前报道的PyAACT/GG共有序列侧翼的核苷酸。