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果蝇探戈bHLH-PAS转录因子转录激活结构域的分析

Analysis of the transcriptional activation domain of the Drosophila tango bHLH-PAS transcription factor.

作者信息

Sonnenfeld Margaret J, Delvecchio Christopher, Sun Xuetao

机构信息

Department of Cellular and Molecular Medicine, University of Ottawa, Ontario, Canada K1H 8M5.

出版信息

Dev Genes Evol. 2005 May;215(5):221-9. doi: 10.1007/s00427-004-0462-9. Epub 2005 Apr 8.

Abstract

Basic-helix-loop-helix-PAS transcription factors play important roles in diverse biological processes including cellular differentiation and specification, oxygen tension regulation and dioxin metabolism. Drosophila tango is orthologous to mammalian Arnt and acts as a common dimerization partner for bHLH-PAS proteins during embryogenesis. A transient transfection assay using Drosophila S2 tissue culture cells and wild-type and mutant Drosophila tango cDNAs was used to localize the activation domain of the Tango protein. An activation domain was identified in the C-terminus of TGO consisting of poly-glutamine and histidine-proline repeats. Transcriptional activation of the fibroblast growth factor receptor (breathless) gene required an intact TGO C-terminus, in vitro. Co-expression assays of trachealess and tgo in the developing eye imaginal disc showed a requirement for the C-terminal transactivation domain of TGO for a cellular response. Genetic analysis of tgo(3) shows that the paired repeat is necessary for tracheal tubule formation in all branches. Lastly, expression of a C-terminal truncated tgo transgene specifically in the CNS midline and trachea resulted in reductions in the number of breathless-expressing cells. These results together identify TGO's transactivation domain and establish its importance for proper target gene regulation and cellular specification.

摘要

碱性螺旋-环-螺旋-PAS转录因子在多种生物学过程中发挥重要作用,包括细胞分化与特化、氧张力调节和二噁英代谢。果蝇的tango与哺乳动物的Arnt直系同源,在胚胎发育过程中作为bHLH-PAS蛋白的共同二聚化伴侣。利用果蝇S2组织培养细胞以及野生型和突变型果蝇tango cDNA进行的瞬时转染试验,用于定位Tango蛋白的激活结构域。在TGO的C末端鉴定出一个激活结构域,其由聚谷氨酰胺和组氨酸-脯氨酸重复序列组成。体外实验表明,成纤维细胞生长因子受体(呼吸缺陷)基因的转录激活需要完整的TGO C末端。在发育中的眼成虫盘进行气管缺失和tgo的共表达试验表明,细胞反应需要TGO的C末端反式激活结构域。对tgo(3)的遗传分析表明,配对重复序列对于所有分支中气管小管的形成是必需的。最后,在中枢神经系统中线和气管中特异性表达C末端截短的tgo转基因,导致表达呼吸缺陷的细胞数量减少。这些结果共同确定了TGO的反式激活结构域,并确立了其对正确的靶基因调控和细胞特化的重要性。

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