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无气管(Trh)在果蝇胚胎发生过程中调节所有气管基因。

Trachealess (Trh) regulates all tracheal genes during Drosophila embryogenesis.

机构信息

Department of Cell Biology, The Johns Hopkins University School of Medicine, 725 N. Wolfe Street, Baltimore, MD 21205–2196, USA

出版信息

Dev Biol. 2011 Dec 1;360(1):160-72. doi: 10.1016/j.ydbio.2011.09.014. Epub 2011 Sep 22.

Abstract

The Drosophila trachea is a branched tubular epithelia that transports oxygen and other gases. trachealess (trh), which encodes a bHLH-PAS transcription factor, is among the first genes to be expressed in the cells that will form the trachea. In the absence of trh, tracheal cells fail to invaginate to form tubes and remain on the embryo surface. Expression of many tracheal-specific genes depends on trh, but all of the known targets have relatively minor phenotypes compared to loss of trh, suggesting that there are additional targets. To identify uncharacterized transcriptional targets of Trh and to further understand the role of Trh in embryonic tracheal formation, we performed an in situ hybridization screen using a library of ~100 tracheal-expressed genes identified by the Berkeley Drosophila Genome Project (BDGP). Surprisingly, expression of every tracheal gene we tested was dependent on Trh, suggesting a major role for Trh in activation and maintenance of tracheal gene expression. A re-examination of the interdependence of the known early-expressed transcription factors, including trh, ventral veinless (vvl) and knirps/knirps-related (kni/knrl), suggests a new model for how gene expression is controlled in the trachea, with trh regulating expression of vvl and kni, but not vice versa. A pilot screen for the targets of Vvl and Kni/Knrl revealed that Vvl and Kni have only minor roles compared to Trh. Finally, genome-wide microarray experiments identified additional Trh targets and revealed that a variety of biological processes are affected by the loss of trh.

摘要

果蝇的气管是一种分支管状上皮组织,用于运输氧气和其他气体。编码 bHLH-PAS 转录因子的 trachealess (trh) 基因是最早在将形成气管的细胞中表达的基因之一。在没有 trh 的情况下,气管细胞无法内陷形成管腔,而仍停留在胚胎表面。许多气管特异性基因的表达依赖于 trh,但与 trh 缺失相比,所有已知的靶基因的表型都相对较小,这表明存在其他靶基因。为了鉴定 Trh 的未被描述的转录靶标,并进一步了解 Trh 在胚胎气管形成中的作用,我们使用伯克利果蝇基因组计划 (BDGP) 鉴定的约 100 个气管表达基因文库进行了原位杂交筛选。令人惊讶的是,我们测试的每个气管基因的表达都依赖于 Trh,这表明 Trh 在激活和维持气管基因表达方面发挥了主要作用。对已知早期表达的转录因子(包括 trh、ventral veinless (vvl) 和 knirps/knirps-related (kni/knrl))的相互依赖性的重新检查表明,气管中基因表达的控制存在一种新模型,trh 调节 vvl 和 kni 的表达,但反之则不然。对 Vvl 和 Kni/Knrl 的靶基因的初步筛选表明,与 Trh 相比,Vvl 和 Kni 的作用较小。最后,全基因组微阵列实验鉴定了其他 Trh 靶标,并表明各种生物过程都受到 trh 缺失的影响。

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