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果蝇眼畸形、无眼双生子和 orthodenticle 基因的遗传相互作用调控小眼发育过程中的 sine oculis 表达。

Genetic interactions of eyes absent, twin of eyeless and orthodenticle regulate sine oculis expression during ocellar development in Drosophila.

机构信息

Biozentrum, University of Basel, Basel, Switzerland.

出版信息

Dev Biol. 2010 Aug 15;344(2):1088-99. doi: 10.1016/j.ydbio.2010.05.494. Epub 2010 May 24.

Abstract

The homeobox gene sine oculis (so) is required for the development of the entire visual system in Drosophila, which includes the compound eyes, the ocelli, the optic lobe of the brain and the Bolwig's organ. During ocelli development, so expression labels, together with eyes absent (eya), the emergence of the ocellar precursor cells in the third instar eye-antennal disc. Footprinting and misexpression studies have led to the proposal that the Pax6 homologue twin of eyeless (toy) directly regulates the initiation of so expression in ocellar precursor cells. However, so expression in a toy loss-of-function mutant background has not been yet analyzed due to the lack of eye-antennal disc development in strong toy mutant alleles. Using an embryonic eye primordium-specific enhancer of toy, we have rescued the developmental defect of a strong toy mutant allele and analyzed so expression in the ocelli primordium of toy loss-of-function eye-antennal discs during third instar larva. The results show that so expression is only marginally affected in the absence of Toy transcriptional activity and that the toy positive effect on so expression is largely eya-mediated. These results suggest that eya is the main factor controlling both initiation and maintenance of so expression in ocellar precursor cells. In addition, we present the characterization of a new minimal eye/ocellus-specific enhancer of the so gene.

摘要

同源盒基因 sine oculis (so) 是果蝇整个视觉系统发育所必需的,包括复眼、小眼、脑的视叶和 Bolwig 氏器。在小眼发育过程中,so 表达标签与 eyes absent (eya) 一起,标记出第三龄眼-触角盘小眼前体细胞的出现。足迹分析和异位表达研究表明,eyeless (toy) 的 Pax6 同源物直接调控小眼前体细胞中 so 表达的起始。然而,由于强 toy 突变等位基因中缺乏眼-触角盘发育,因此尚未分析 toy 功能丧失突变背景中的 so 表达。利用 toy 的一个胚胎眼原基特异性增强子,我们挽救了一个强 toy 突变等位基因的发育缺陷,并在第三龄幼虫的 toy 功能丧失的眼-触角盘中分析了 so 在小眼原基中的表达。结果表明,在没有 Toy 转录活性的情况下,so 表达仅受到轻微影响,而 toy 对 so 表达的正效应在很大程度上是通过 eya 介导的。这些结果表明,eya 是控制小眼前体细胞中 so 表达起始和维持的主要因素。此外,我们还介绍了 so 基因的一个新的最小眼/小眼特异性增强子的特征。

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