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果蝇视网膜决定基因腊肠眼的两个眼特异性增强子的双重调控和冗余功能

Dual regulation and redundant function of two eye-specific enhancers of the Drosophila retinal determination gene dachshund.

作者信息

Pappu Kartik S, Ostrin Edwin J, Middlebrooks Brooke W, Sili Beril Tavsanli, Chen Rui, Atkins Mardelle R, Gibbs Richard, Mardon Graeme

机构信息

Program in Developmental Biology, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.

出版信息

Development. 2005 Jun;132(12):2895-905. doi: 10.1242/dev.01869.

Abstract

Drosophila eye development is controlled by a conserved network of retinal determination (RD) genes. The RD genes encode nuclear proteins that form complexes and function in concert with extracellular signal-regulated transcription factors. Identification of the genomic regulatory elements that govern the eye-specific expression of the RD genes will allow us to better understand how spatial and temporal control of gene expression occurs during early eye development. We compared conserved non-coding sequences (CNCSs) between five Drosophilids along the approximately 40 kb genomic locus of the RD gene dachshund (dac). Our analysis uncovers two separate eye enhancers in intron eight and the 3' non-coding regions of the dac locus defined by clusters of highly conserved sequences. Loss- and gain-of-function analyses suggest that the 3' eye enhancer is synergistically activated by a combination of eya, so and dpp signaling, and only indirectly activated by ey, whereas the 5' eye enhancer is primarily regulated by ey, acting in concert with eya and so. Disrupting conserved So-binding sites in the 3' eye enhancer prevents reporter expression in vivo. Our results suggest that the two eye enhancers act redundantly and in concert with each other to integrate distinct upstream inputs and direct the eye-specific expression of dac.

摘要

果蝇眼睛发育受视网膜决定(RD)基因的保守网络控制。RD基因编码核蛋白,这些核蛋白形成复合物并与细胞外信号调节转录因子协同发挥作用。鉴定调控RD基因眼睛特异性表达的基因组调控元件,将使我们能够更好地理解在眼睛早期发育过程中基因表达的时空控制是如何发生的。我们比较了五种果蝇在RD基因腊肠犬(dac)约40 kb基因组位点上的保守非编码序列(CNCSs)。我们的分析在dac基因座的第八内含子和3'非编码区发现了两个独立的眼睛增强子,它们由高度保守序列簇定义。功能丧失和功能获得分析表明,3'眼睛增强子由eya、so和dpp信号的组合协同激活,仅由ey间接激活,而5'眼睛增强子主要由ey调控,与eya和so协同作用。破坏3'眼睛增强子中保守的So结合位点可阻止报告基因在体内表达。我们的结果表明,这两个眼睛增强子相互冗余并协同作用,以整合不同的上游输入并指导dac的眼睛特异性表达。

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