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Cooperation of axial and sex specific information controls Drosophila female genitalia growth by regulating the Decapentaplegic pathway

机译:轴向和性别特异性信息的合作通过调节黛比恩肺途径来控制果蝇女性生殖器生长

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摘要

The specification and morphogenesis of an organ requires the coordinate deployment and integration of regulatory information, including sex specific information when the organ is sex specific. Only a few gene networks controlling size and pattern development have been deciphered, which limits the emergence of principles, general or not, underlying the organ-specifying gene networks. Here we elucidate the genetic and molecular network determining the control of size in the Drosophila abdominal A9 primordium, contributing to the female genitalia. This network requires axial regulatory information provided by the Hox protein Abdominal-BR (Abd-BR), the Hox cofactors Extradenticle (Exd) and Homothorax (Hth), and the sex specific transcription factor Doublesex Female (DsxF). These factors synergize to control size in the female A9 by the coordinate regulation of the Decapentaplegic (Dpp) growth pathway. Molecular dissection of the dpp regulatory region and in vivo protein interaction experiments suggest that Abd-BR, Exd, Hth and DsxF coordinately regulate a short dpp enhancer to repress dpp expression and restrict female A9 size. The same regulators can also suppress dpp expression in the A8, but this requires the absence of the Abd-BM isoform, which specifies A8. These results delineate the network controlling female A9 growth in Drosophila.
机译:器官的规范和形态发生需要协调部署和整合法规信息,包括当器官特定的性别特定信息。仅破坏了少数基因网络控制尺寸和模式开发,这限制了器官指定基因网络的原则,一般与否的出现。在这里,我们阐明遗传和分子网络确定果蝇腹部A9原基中的大小的控制,有助于雌性生殖器。该网络需要由Hox蛋白腹部 - BR(ABD-BR)提供的轴向调节信息,Hox Cofactors外肠(EXD)和Homothorax(Hth),以及性特异性转录因子Doublesex女性(DSXF)。这些因素通过甲板向内(DPP)生长途径的坐标调节来协同对雌性A9中的控制尺寸。 DPP调节区和体内蛋白质相互作用实验的分子解剖表明ABD-BR,EXD,HTH和DSXF协调,调节短DPP增强剂以压制DPP表达并限制雌性A9尺寸。相同的调节剂也可以抑制A8中的DPP表达,但这需要没有ABD-BM同种型,其指定A8。这些结果描绘了网络控制果蝇的雌性A9生长。

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