Nardelli J, Gibson T, Charnay P
Laboratoire de Génétique Moléculaire, CNRS D 1302, Ecole Normale Supérieure, Paris, France.
Nucleic Acids Res. 1992 Aug 25;20(16):4137-44. doi: 10.1093/nar/20.16.4137.
Zinc fingers of the Cys2/His2 class are conserved 28-30 amino acid motifs that constitute an important and widespread family of eukaryotic DNA-binding domains. It is therefore of great interest to understand the rules that govern specific recognition of DNA by zinc fingers. The DNA-binding domain of the transcription factor Krox-20 consists of three zinc fingers, each of them making its primary contacts with a three-base pair subsite. We have performed a data base-guided site-directed mutagenesis analysis of Krox-20: nine derivatives were generated, in which one to three amino acid changes had been introduced within finger 2, at positions which were likely to affect the specificity of DNA recognition. The affinities of the different proteins for a panel of potential DNA binding sites were estimated by gel retardation assay. Six of the derivatives bound specific targets with affinities comparable to that of wild type Krox-20 for its consensus binding site. However, the specificity of recognition was dramatically modified at the expected bases, in a manner that could be explained by examining the newly introduced amino acids within the context of the overall finger/triplet interaction. These data provide new insights into the details of zinc finger-DNA interactions and, combined with the modular nature of zinc fingers, illustrate both the potential and the difficulties of utilising these motifs for designing DNA-binding proteins with novel specificities.
Cys2/His2类锌指是保守的28 - 30个氨基酸基序,构成了真核生物DNA结合结构域中一个重要且广泛存在的家族。因此,了解锌指对DNA进行特异性识别的规则具有重要意义。转录因子Krox - 20的DNA结合结构域由三个锌指组成,每个锌指主要与一个三碱基对亚位点相互作用。我们对Krox - 20进行了基于数据库的定点诱变分析:生成了九个衍生物,其中在锌指2内可能影响DNA识别特异性的位置引入了一到三个氨基酸变化。通过凝胶阻滞试验估计了不同蛋白质对一组潜在DNA结合位点的亲和力。六个衍生物与特定靶标的结合亲和力与野生型Krox - 20对其共有结合位点的亲和力相当。然而,识别特异性在预期碱基处发生了显著改变,这种改变可以通过在整个锌指/三联体相互作用的背景下检查新引入的氨基酸来解释。这些数据为锌指与DNA相互作用的细节提供了新的见解,并且结合锌指的模块化性质,阐明了利用这些基序设计具有新特异性的DNA结合蛋白的潜力和困难。