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果蝇无眼基因眼部增强子的功能分析:眼部特异性基因的差异调控

Functional analysis of an eye enhancer of the Drosophila eyes absent gene: differential regulation by eye specification genes.

作者信息

Bui Q T, Zimmerman J E, Liu H, Gray-Board G L, Bonini N M

机构信息

Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania, 19104-6018, USA.

出版信息

Dev Biol. 2000 May 15;221(2):355-64. doi: 10.1006/dbio.2000.9688.

Abstract

Genes involved in eye development are highly conserved between vertebrates and Drosophila. Given the complex genetic network controlling early eye development, identification of regulatory sequences controlling gene expression will provide valuable insights toward understanding central events of early eye specification. We have focused on defining regulatory elements critical for Drosophila eyes absent (eya) expression. Although eya has a complex expression pattern during development, analysis of eye-specific mutations in the gene revealed a region selectively deleted in the eye-specific alleles. Here we have performed detailed analysis of the region deleted in the eye-specific eya(2) allele. This analysis shows that this region can direct early eya gene expression in a pattern consistent with that of normal eya in eye progenitor cells. Functional studies indicate that this element will restore appropriate eya transcript expression to rescue the eye-specific allele. We have examined regulation of this element during eye specification, both in normal eye development and in ectopic eye formation. These studies demonstrate that the element was activated upon ectopic expression of the eye specification genes eyeless and dachshund, but does not respond to ectopic expression of eya or sine oculis. The differential regulation of this element by genes involved during early retinal formation reveals new aspects of the genetic hierarchy of eye development.

摘要

参与眼睛发育的基因在脊椎动物和果蝇之间高度保守。鉴于控制早期眼睛发育的复杂遗传网络,鉴定控制基因表达的调控序列将为理解早期眼睛特化的核心事件提供有价值的见解。我们专注于定义对果蝇无眼(eya)基因表达至关重要的调控元件。尽管eya在发育过程中具有复杂的表达模式,但对该基因中眼睛特异性突变的分析揭示了一个在眼睛特异性等位基因中选择性缺失的区域。在此,我们对眼睛特异性eya(2)等位基因中缺失的区域进行了详细分析。该分析表明,该区域能够以与眼睛祖细胞中正常eya一致的模式指导eya基因的早期表达。功能研究表明,该元件将恢复适当的eya转录本表达以挽救眼睛特异性等位基因。我们研究了在正常眼睛发育和异位眼形成过程中,该元件在眼睛特化过程中的调控情况。这些研究表明,该元件在眼睛特异性基因无眼和腊肠眼的异位表达时被激活,但对eya或无眼的异位表达无反应。早期视网膜形成过程中相关基因对该元件的差异调控揭示了眼睛发育遗传层次的新方面。

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