White R A, Aspland S E, Brookman J J, Clayton L, Sproat G
Department of Anatomy, University of Cambridge, Downing Street, Cambridge, UK.
Mech Dev. 2000 Mar 1;91(1-2):217-26. doi: 10.1016/s0925-4773(99)00306-8.
We have shown that the 26 bp bx1 element from the regulatory region of Distal-less is capable of imposing control by the homeotic genes Ultrabithorax and abdominal-A on a general epidermal activator in Drosophila. This provides us with an assay to analyze the sequence requirements for specific repression by these Hox genes. Both the core Hox binding site, 5'-TAAT, and the adjacent EXD 5'-TGAT core site are required for repression by Ultrabithorax and abdominal-A. The Distal-less bx1 site thus fits with the model of Hox protein binding specificity based on the consensus PBX/HOX-family site TGATNNAT[g/t][g/a], where the key elements of binding specificity are proposed to lie in the two base pairs following the TGAT. A single base pair deletion in the bx1 sequence generates a site, bx1:A(-)mut, that on the consensus PBX/HOX model would be expected to be regulated by the Deformed Hox gene. We observed, however, that the bx1:A(-)mut site was regulated predominantly by Sex combs reduced, Ultrabithorax and abdominal-A. The analysis of this site indicates that the specificity of action of Hox proteins may depend not only on selective DNA binding but also on specific post-binding interactions.
我们已经证明,来自无翅基因调控区的26个碱基对的bx1元件能够使同源异型基因超双胸和腹部-A对果蝇中的一种普通表皮激活因子进行调控。这为我们提供了一种分析这些Hox基因特异性抑制的序列要求的方法。超双胸和腹部-A进行抑制需要核心Hox结合位点5'-TAAT以及相邻的EXD 5'-TGAT核心位点。因此,无翅基因的bx1位点符合基于共有PBX/HOX家族位点TGATNNAT[g/t][g/a]的Hox蛋白结合特异性模型,其中结合特异性的关键元件被认为位于TGAT之后的两个碱基对中。bx1序列中的单个碱基对缺失产生了一个位点bx1:A(-)mut,根据共有PBX/HOX模型,预计该位点将由变形Hox基因调控。然而,我们观察到bx1:A(-)mut位点主要受性梳减少、超双胸和腹部-A的调控。对该位点的分析表明,Hox蛋白的作用特异性可能不仅取决于选择性DNA结合,还取决于特定的结合后相互作用。