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在其自身基因的自调控元件、无眼增强子以及信号基因刺猬蛋白中鉴定功能性眼原基基序。

Identification of functional sine oculis motifs in the autoregulatory element of its own gene, in the eyeless enhancer and in the signalling gene hedgehog.

作者信息

Pauli Tobias, Seimiya Makiko, Blanco Jorge, Gehring Walter J

机构信息

Biozentrum, University of Basel, Klingelbergstrasse 70, CH-4056 Basel, Switzerland.

出版信息

Development. 2005 Jun;132(12):2771-82. doi: 10.1242/dev.01841. Epub 2005 May 18.

DOI:10.1242/dev.01841
PMID:15901665
Abstract

In Drosophila, the sine oculis (so) gene is important for the development of the entire visual system, including Bolwig's organ, compound eyes and ocelli. Together with twin of eyeless, eyeless, eyes absent and dachshund, so belongs to a network of genes that by complex interactions initiate eye development. Although much is known about the genetic interactions of the genes belonging to this retinal determination network, only a few such regulatory interactions have been analysed down to the level of DNA-protein interactions. Previous work in our laboratory identified an eye/ocellus specific enhancer of the sine oculis gene that is directly regulated by eyeless and twin of eyeless. We further characterized this regulatory element and identified a minimal enhancer fragment of so that sets up an autoregulatory feedback loop crucial for proper ocelli development. By systematic analysis of the DNA-binding specificity of so we identified the most important nucleotides for this interaction. Using the emerging consensus sequence for SO-DNA binding we performed a genome-wide search and have thereby been able to identify eyeless as well as the signalling gene hedgehog as putative targets of so. Our results strengthen the general assumption that feedback loops among the genes of the retinal determination network are crucial for proper development of eyes and ocelli.

摘要

在果蝇中,无眼基因(so)对于整个视觉系统的发育至关重要,包括博尔维格氏器官、复眼和单眼。so与无眼的孪生基因、无眼基因、缺眼基因和腊肠犬基因一起,属于一个基因网络,这些基因通过复杂的相互作用启动眼睛发育。尽管对于属于这个视网膜决定网络的基因的遗传相互作用已经了解很多,但只有少数这样的调控相互作用被分析到DNA-蛋白质相互作用的水平。我们实验室之前的工作鉴定出了一个无眼基因的眼/单眼特异性增强子,它直接受无眼的孪生基因和无眼基因调控。我们进一步对这个调控元件进行了表征,并鉴定出了so的一个最小增强子片段,该片段建立了一个对单眼正常发育至关重要的自调控反馈环。通过对so的DNA结合特异性进行系统分析,我们确定了这种相互作用中最重要的核苷酸。利用新出现的SO-DNA结合共有序列,我们进行了全基因组搜索,从而能够鉴定出无眼基因以及信号基因刺猬基因作为so的假定靶标。我们的结果强化了一个普遍的假设,即视网膜决定网络中的基因之间的反馈环对于眼睛和单眼的正常发育至关重要。

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