Tanikawa J, Yasukawa T, Enari M, Ogata K, Nishimura Y, Ishii S, Sarai A
Graduate School of Integrated Science, Yokohama City University, Japan.
Proc Natl Acad Sci U S A. 1993 Oct 15;90(20):9320-4. doi: 10.1073/pnas.90.20.9320.
The DNA-binding domain of c-Myb consists of three homologous tandem repeats of 52 amino acids. The structure of the third (C-terminal) repeat obtained by NMR analysis has a conformation related to the helix-turn-helix motif. To identify the role of each repeat in the sequence recognition of DNA, we analyzed specific interactions between c-Myb and DNA by measuring binding affinities for systematic mutants of Myb-binding DNA sites and various truncated c-Myb mutants. We found that specific interactions are localized unevenly in the AACTGAC region in the consensus binding site of c-Myb: The first adenine, third cytosine, and fifth guanine are involved in very specific interactions, in which any base substitutions reduce the binding affinity by > 500-fold. On the other hand, the interaction at the second adenine is less specific, with the affinity reduction in the range of 6- to 15-fold. The seventh cytosine involves a rather peculiar interaction, in which only guanine substitution abolishes the specific binding. The binding analyses, together with the chemical protection analyses, showed that the c-Myb fragment containing the second and third repeats covers the AACTGAC region from the major groove of DNA in such an orientation that the third repeat covers the core AAC sequence. These results suggest that the third repeat recognizes the core AAC sequence very specifically, whereas the second repeat recognizes the GAC sequence in a more redundant manner. The first (N-terminal) repeat, which covers the major groove of DNA only partially, is not significant in the sequence recognition, but it contributes to increase the stability of the Myb-DNA complex. The presence of an N-terminal acidic region upstream of the first repeat, which is important for the activation of c-myb protooncogene, was found to reduce the binding affinity by interfering with the first repeat in binding to DNA.
c-Myb的DNA结合结构域由三个52个氨基酸的同源串联重复序列组成。通过核磁共振分析获得的第三个(C端)重复序列的结构具有与螺旋-转角-螺旋基序相关的构象。为了确定每个重复序列在DNA序列识别中的作用,我们通过测量c-Myb与Myb结合DNA位点的系统突变体以及各种截短的c-Myb突变体的结合亲和力,分析了c-Myb与DNA之间的特异性相互作用。我们发现,特异性相互作用在c-Myb共有结合位点的AACTGAC区域分布不均:第一个腺嘌呤、第三个胞嘧啶和第五个鸟嘌呤参与非常特异性的相互作用,其中任何碱基替换都会使结合亲和力降低500倍以上。另一方面,第二个腺嘌呤处的相互作用特异性较低,亲和力降低6至15倍。第七个胞嘧啶涉及一种相当特殊的相互作用,只有鸟嘌呤替换会消除特异性结合。结合分析以及化学保护分析表明,包含第二个和第三个重复序列的c-Myb片段以这样一种方向覆盖DNA大沟中的AACTGAC区域,即第三个重复序列覆盖核心AAC序列。这些结果表明,第三个重复序列非常特异性地识别核心AAC序列,而第二个重复序列以更冗余的方式识别GAC序列。第一个(N端)重复序列仅部分覆盖DNA大沟,在序列识别中不显著,但它有助于增加Myb-DNA复合物的稳定性。发现在第一个重复序列上游存在一个N端酸性区域,这对c-myb原癌基因的激活很重要,它通过干扰第一个重复序列与DNA的结合来降低结合亲和力。