PROXIMODISTAL AXIS AND TISSUE SPECIFIC GENE REGULATION

这项建议中概述的实验的目的是解决发育中的两个基本问题：近端/远端(P/D)轴是如何在发育中的肢体形成的，以及如何区分不同的肢体类型。我们的工作集中在由Dll基因编码的同源结构域转录因子的遗传和生化相互作用上。Dll是已知最早在发育中的昆虫肢体中特异表达的基因，在异位表达时可以启动P/D轴的形成，是触角、腿和肢体衍生的颌骨结构中P/D模式元件的形成所必需的，在区分果蝇触角和腿的过程中起着至关重要的作用。D11的不同发育作用可能是通过不同的靶基因组来调节的。然而，D11本身几乎没有DNA结合特异性，我们假设，组织和区域特异性与不同辅助因子的相互作用是D11实现调节不同靶点所需的特异性所必需的。因此，如果我们想要了解D11促进肢体发育的机制，我们必须同时识别D11辅助因子和D11靶基因。利用遗传学方法，我们已经确定Spalt(Sal)是触角中D11调节的靶标，同胸(HTH)和牙外环(EXD)可能是D11调节Sal的辅助因子。在这里，我们建议扩展我们的遗传学研究，以确定其他假定的靶标和辅助因子，并使用分子和生化方法来识别靶基因增强子中的D11反应元件，如SAL的atenna1增强子，并测试D11、HTH和EXD之间的物理相互作用。由于D11同源基因(DLX基因)在包括脊椎动物在内的至少六个腔脊椎动物的发育附件中表达，我们预计拟议的研究将为脊椎动物以及节肢动物的肢体发育提供见解。此外，由于哺乳动物的DLX基因是正常大脑和颧弓发育所必需的，我们预计从这些实验中获得的机制见解也将增加我们对DLL和D1x在肢体以外的组织和器官中功能的理解。

The aim of the experiments outlined in this proposal is to address two fundamental issues in development: how the proximodistal (P/D) axis is formed in developing limbs and what distinguishes different limb types from one another. Our efforts are focused on the genetic and biochemical interactions of a homeodomain transcription factor encoded by the Drosophila Distal-less (Dll) gene. Dll is the earliest known gene to be specifically expressed in developing insect limbs, can initiate P/D axis formation when expressed ectopically, is required for the elaboration of P/D pattern elements in the antenna, the legs and the limb-derived gnathal structures, and plays an essential role in distinguishing the Drosophila antenna from the leg. The distinct developmental roles of D11 are likely to be mediated via distinct suites of target genes. However, D11 has little DNA binding specificity of its own, and we hypothesize that tissue and domain specific interactions with different co-factors are essential for D11 to achieve the specificity needed to regulate distinct targets. Therefore, if we want to understand the mechanisms by which D11 contributes to limb development, we must identify both D11 co-factors and D11 target genes. Using genetic approaches, we have identified spalt (sal) as a target of D11 regulation in the antenna and Homothorax (Hth) and Extradenticle (Exd) as a putative co-factors of D11 for the regulation of sal. Here, we propose to extend our genetic studies to identify other putative targets and co-factors and to use molecular and biochemical approaches both to identify the D11 responsive elements in target gene enhancers, such as the atenna1 enhancers of sal, and to test for physical interactions among D11, Hth and Exd. Because D11 homologs (the Dlx genes) are expressed in developing appendages in at least six coelomate phyla, including vertebrates we anticipate that the proposed studies will provide insights into vertebrate, as well as arthropod, limb development. In addition, since mammalian Dlx genes are required for aspects of normal brain and branchial arch development, we expect that the mechanistic insights gained from these experiments also will increase our understanding of Dll and D1x function in tissues and organs other than limbs.