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无眼基因是果蝇视觉系统发育所需的一种同源异型盒基因。

sine oculis is a homeobox gene required for Drosophila visual system development.

作者信息

Serikaku M A, O'Tousa J E

机构信息

Department of Biological Sciences, University of Notre Dame, Indiana 46556.

出版信息

Genetics. 1994 Dec;138(4):1137-50. doi: 10.1093/genetics/138.4.1137.

DOI:10.1093/genetics/138.4.1137
PMID:7896096
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1206253/
Abstract

The somda (sine oculis-medusa) mutant is the result of a P element insertion at position 43C on the second chromosome. somda causes aberrant development of the larval photoreceptor (Bolwig's) organ and the optic lobe primordium in the embryo. Later in development, adult photoreceptors fail to project axons into the optic ganglion. Consequently optic lobe development is aborted and photoreceptor cells show age-dependent retinal degeneration. The so gene was isolated and characterized. The gene encodes a homeodomain protein expressed in the optic lobe primordium and Bolwig's organ of embryos, in the developing adult visual system of larvae, and in photoreceptor cells and optic lobes of adults. In addition, the SO product is found at invagination sites during embryonic development: at the stomadeal invagination, the cephalic furrow, and at segmental boundaries. The mutant somda allele causes severe reduction of SO embryonic expression but maintains adult visual system expression. Ubiquitous expression of the SO gene product in 4-8-hr embryos rescues all somda mutant abnormalities, including the adult phenotypes. Thus, all deficits in adult visual system development and function results from failure to properly express the so gene during embryonic development. This analysis shows that the homeodomain containing SO gene product is involved in the specification of the larval and adult visual system development during embryogenesis.

摘要

somda(无眼-美杜莎)突变体是由于P因子插入到第二条染色体上的43C位置所致。somda导致幼虫光感受器(博尔维格氏)器官和胚胎中视叶原基的异常发育。在发育后期,成年光感受器无法将轴突投射到视神经节。因此,视叶发育中止,光感受器细胞呈现出与年龄相关的视网膜退化。so基因被分离并进行了表征。该基因编码一种同源结构域蛋白,在胚胎的视叶原基和博尔维格氏器官、幼虫发育中的成年视觉系统以及成年个体的光感受器细胞和视叶中表达。此外,在胚胎发育过程中的内陷部位也能发现SO产物:在口凹内陷、头部沟以及体节边界处。突变的somda等位基因导致SO胚胎表达严重减少,但维持成年视觉系统表达。在4-8小时胚胎中普遍表达SO基因产物可挽救所有somda突变异常,包括成年表型。因此,成年视觉系统发育和功能的所有缺陷都是由于胚胎发育期间未能正确表达so基因所致。该分析表明,含有同源结构域的SO基因产物在胚胎发生过程中参与了幼虫和成年视觉系统发育的特化。