Yamazaki Haruka, Tomono Ayami, Ohnishi Yasuo, Horinouchi Sueharu
Department of Biotechnology, Graduate School of Agriculture and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan.
Mol Microbiol. 2004 Jul;53(2):555-72. doi: 10.1111/j.1365-2958.2004.04153.x.
AdpA, belonging to the AraC/XylS family, is the key transcriptional activator for a number of genes of various functions in the A-factor regulatory cascade in Streptomyces griseus. It consists of a ThiJ/PfpI/DJ-1-like dimerization domain at its N-terminal portion and a DNA-binding domain with two helix-turn-helix motifs at its C-terminal portion, representing a large subgroup of the AraC/XylS family. Uracil interference assay and missing T and GA interference assays on several AdpA binding sites, followed by gel mobility shift assays on systematically mutated binding sites, revealed a consensus AdpA-binding sequence, 5'-TGGCSNGWWY-3' (S: G or C; W: A or T; Y: T or C; N: any nucleotide). A dimer of AdpA bound a site including the two consensus sequences, with a space of 13-14 bp, as an inverted repeat (type I) at various positions, for example more than 200 bp upstream (-200) and 25 bp downstream (+25) from the transcriptional start point of the target gene. In addition, AdpA also bound a site including the consensus sequence in a single copy (type II) at positions, in most cases, from -40 to -50 and from -50 to -60. For transcriptional activation, some genes required simultaneous binding of a dimer of AdpA to type I and II sites, but others required only a single type I or type II site. AdpA bound mutated type I sites with various distances between the two consensus sequences with significant affinities, although the optimal distances for AdpA to bind were 13-14 bp and 2 bp. The DNA-binding domain is therefore connected to the ThiJ/PfpI/DJ-1-like dimerization domain with a flexible linker. The DNA-binding specificity of AdpA in conjunction with that of other AraC/XylS family members is discussed.
AdpA属于AraC/XylS家族,是灰色链霉菌A因子调控级联中多种功能基因的关键转录激活因子。它在N端部分包含一个ThiJ/PfpI/DJ-1样二聚化结构域,在C端部分有一个带有两个螺旋-转角-螺旋基序的DNA结合结构域,代表了AraC/XylS家族的一个大亚组。对几个AdpA结合位点进行尿嘧啶干扰试验和缺失T及GA干扰试验,随后对系统突变的结合位点进行凝胶迁移率变动分析,揭示了一个共有AdpA结合序列5'-TGGCSNGWWY-3'(S:G或C;W:A或T;Y:T或C;N:任意核苷酸)。AdpA二聚体结合一个包含两个共有序列的位点,两个共有序列之间间隔13 - 14 bp,呈反向重复(I型),位于不同位置,例如在靶基因转录起始点上游超过200 bp(-200)和下游25 bp(+25)处。此外,AdpA还在大多数情况下在-40至-50以及-50至-60的位置结合一个单拷贝的包含共有序列的位点(II型)。对于转录激活,一些基因需要AdpA二聚体同时结合I型和II型位点,但其他基因只需要单个I型或II型位点。AdpA以显著亲和力结合两个共有序列之间具有不同距离的突变I型位点,尽管AdpA结合的最佳距离是13 - 14 bp和2 bp。因此,DNA结合结构域通过一个柔性接头与ThiJ/PfpI/DJ-1样二聚化结构域相连。本文还讨论了AdpA与其他AraC/XylS家族成员结合的DNA特异性。