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单 minded、Dmef2、Pointed 和 Su(H)作用于黑腹果蝇中最粗糙基因的特定调控序列。

Single-minded, Dmef2, Pointed, and Su(H) act on identified regulatory sequences of the roughest gene in Drosophila melanogaster.

作者信息

Apitz Holger, Strünkelnberg Martin, de Couet Heinz Gert, Fischbach Karl-Friedrich

机构信息

Institut für Biologie III, Albert-Ludwigs-Universität Freiburg, Schänzlestr.1, 79104, Freiburg, Germany.

出版信息

Dev Genes Evol. 2005 Sep;215(9):460-69. doi: 10.1007/s00427-005-0005-z. Epub 2005 Aug 11.

Abstract

Roughest (Rst) is a cell adhesion molecule of the immunoglobulin superfamily that has multiple and diverse functions during the development of Drosophila melanogaster. The pleiotropic action of Rst is reflected by its complex and dynamic expression during the development of Drosophila. By an enhancer detection screen, we previously identified several cis-regulatory modules that mediate specific expression of the roughest gene in Drosophila developmental processes. To identify trans-regulators of rst expression, we used the Gal4/UAS system to screen for factors that were sufficient to activate Rst expression when ectopically expressed. By this method we identified the transcription factors Single-minded, Pointed.P1, and Su(H)-VP16. Furthermore, we showed that these factors and, in addition, Dmef2 are able to ectopically activate rst expression via the previously described rst cis-regulatory modules. This fact and the use of mutant analysis allocates the action of the transcription factors to specific developmental contexts. In the case of Sim, we could show that it regulates rst expression in the embryonic midline, but not in the optic lobes. Mutagenesis of Sim consensus binding sites in the regulatory module required for rst expression in the embryonic midline, abolished rst expression; indicating that the regulation of rst by Sim is direct.

摘要

糙面(Rst)是免疫球蛋白超家族的一种细胞粘附分子,在黑腹果蝇发育过程中具有多种不同功能。Rst的多效性作用体现在其在果蝇发育过程中复杂且动态的表达上。通过增强子检测筛选,我们之前鉴定出了几个顺式调控模块,它们在果蝇发育过程中介导糙面基因的特异性表达。为了鉴定rst表达的反式调节因子,我们使用Gal4/UAS系统筛选异位表达时足以激活Rst表达的因子。通过这种方法,我们鉴定出了转录因子单 minded、Pointed.P1和Su(H)-VP16。此外,我们表明这些因子以及Dmef2能够通过先前描述的rst顺式调控模块异位激活rst表达。这一事实以及突变分析的使用将转录因子的作用分配到了特定的发育背景中。就Sim而言,我们能够证明它在胚胎中线调节rst表达,但在视叶中不调节。胚胎中线rst表达所需调控模块中Sim共有结合位点的诱变消除了rst表达;这表明Sim对rst的调节是直接的。

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