Ebner Andreas, Cabernard Clemens, Affolter Markus, Merabet Samir
Biozentrum der Universität Basel, Klingelbergstrasse 70, CH-4056 Basel, Switzerland.
Development. 2005 Apr;132(7):1591-600. doi: 10.1242/dev.01721.
Hox genes encode evolutionarily conserved transcriptional regulators, which define regional identities along the anteroposterior axis of multicellular animals. In Drosophila, Hox proteins bind to target DNA sequences in association with the Extradenticle (Exd) and Homothorax (Hth) co-factors. The current model of Hox-binding selectivity proposes that the nucleotide sequence identity defines the Hox protein engaged in the trimeric complex, implying that distinct Hox/Exd/Hth complexes select different binding sites and that a given Hox/Exd/Hth complex recognizes a consensus DNA sequence. Here, we report that the regulation of a newly identified Lab target gene does not rely on the previously established consensus Lab/Exd/Hth-binding site, but on a strongly divergent sequence. Thus Lab, and most probably other Hox proteins, selects different DNA sequences in regulating downstream target genes. These observations have implications with regard to the current model of Hox-binding selectivity.
Hox基因编码进化上保守的转录调节因子,这些因子决定多细胞动物前后轴上的区域特性。在果蝇中,Hox蛋白与额外齿状蛋白(Exd)和同胸蛋白(Hth)辅助因子结合,以靶向DNA序列。当前关于Hox结合选择性的模型提出,核苷酸序列一致性决定了参与三聚体复合物的Hox蛋白,这意味着不同的Hox/Exd/Hth复合物选择不同的结合位点,且给定的Hox/Exd/Hth复合物识别一个共有DNA序列。在此,我们报告一个新鉴定的Lab靶基因的调控并不依赖于先前确立的共有Lab/Exd/Hth结合位点,而是依赖于一个差异很大的序列。因此,Lab以及极有可能的其他Hox蛋白在调节下游靶基因时选择不同的DNA序列。这些观察结果对当前的Hox结合选择性模型具有启示意义。