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果蝇变态过程中,DHR3孤儿受体对幼虫和蛹前期基因表达的协调作用。

Coordination of larval and prepupal gene expression by the DHR3 orphan receptor during Drosophila metamorphosis.

作者信息

Lam G T, Jiang C, Thummel C S

机构信息

Howard Hughes Medical Institute, University of Utah, Salt Lake City 84112, USA.

出版信息

Development. 1997 May;124(9):1757-69. doi: 10.1242/dev.124.9.1757.

Abstract

The DHR3 orphan receptor gene is induced directly by the steroid hormone ecdysone at the onset of Drosophila metamorphosis. DHR3 expression peaks in early prepupae, as the early puff genes are repressed and betaFTZ-F1 is induced. Here we provide evidence that DHR3 directly contributes to both of these regulatory responses. DHR3 protein is bound to many ecdysone-induced puffs in the polytene chromosomes, including the early puffs that encode the BR-C and E74 regulatory genes, as well as the E75, E78 and betaFTZ-F1 orphan receptor loci. Three DHR3 binding sites were identified downstream from the start site of betaFTZ-F1 transcription, further indicating that this gene is a direct target of DHR3 regulation. Ectopic expression of DHR3 revealed that the polytene chromosome binding pattern is of functional significance. DHR3 is sufficient to repress BR-C, E74A, E75A and E78B transcription as well as induce betaFTZ-F1. DHR3 thus appears to function as a switch that defines the larval-prepupal transition by arresting the early regulatory response to ecdysone at puparium formation and facilitating the induction of the betaFTZ-F1 competence factor in mid-prepupae. This study also provides evidence for direct cross-regulation among orphan members of the nuclear receptor superfamily and further implicates these genes as critical transducers of the hormonal signal during the onset of Drosophila metamorphosis.

摘要

在果蝇变态发育开始时,类固醇激素蜕皮激素可直接诱导DHR3孤儿受体基因。随着早期胀泡基因被抑制且βFTZ - F1被诱导,DHR3的表达在早蛹期达到峰值。在此,我们提供证据表明DHR3直接参与了这两种调节反应。DHR3蛋白与多线染色体中许多蜕皮激素诱导的胀泡结合,包括编码BR - C和E74调节基因的早期胀泡,以及E75、E78和βFTZ - F1孤儿受体基因座。在βFTZ - F1转录起始位点下游鉴定出三个DHR3结合位点,进一步表明该基因是DHR3调节的直接靶点。DHR3的异位表达表明多线染色体结合模式具有功能意义。DHR3足以抑制BR - C、E74A、E75A和E78B的转录,并诱导βFTZ - F1。因此,DHR3似乎起到了一个开关的作用,通过在蛹化时阻止对蜕皮激素的早期调节反应,并促进在早蛹中期诱导βFTZ - F1感受态因子,来定义幼虫 - 早蛹转变。这项研究还为核受体超家族孤儿成员之间的直接交叉调节提供了证据,并进一步表明这些基因是果蝇变态发育开始期间激素信号的关键转导因子。

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