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在果蝇变态发育开始期间,蜕皮甾体信号传导需要DHR78核受体。

The DHR78 nuclear receptor is required for ecdysteroid signaling during the onset of Drosophila metamorphosis.

作者信息

Fisk G J, Thummel C S

机构信息

Howard Hughes Medical Institute, Department of Human Genetics, University of Utah, Salt Lake City 84112-5331, USA.

出版信息

Cell. 1998 May 15;93(4):543-55. doi: 10.1016/s0092-8674(00)81184-8.

Abstract

Pulses of ecdysteroids direct Drosophila through its life cycle by activating stage- and tissue-specific genetic regulatory hierarchies. Here we show that an orphan nuclear receptor, DHR78, functions at the top of the ecdysteroid regulatory hierarchies. Null mutations in DHR78 lead to lethality during the third larval instar with defects in ecdysteroid-triggered developmental responses. Consistent with these phenotypes, DHR78 mutants fail to activate the mid-third instar regulatory hierarchy that prepares the animal for metamorphosis. DHR78 protein is bound to many ecdysteroid-regulated puff loci, suggesting that DHR78 directly regulates puff gene expression. In addition, ectopic expression of DHR78 has no effects on development, indicating that its activity is regulated post-translationally. We propose that DHR78 is a ligand-activated receptor that plays a central role in directing the onset of Drosophila metamorphosis.

摘要

蜕皮甾体脉冲通过激活特定阶段和组织的遗传调控层级,引导果蝇度过其生命周期。在此我们表明,一种孤儿核受体DHR78在蜕皮甾体调控层级的顶端发挥作用。DHR78的无效突变导致第三龄幼虫期致死,并伴有蜕皮甾体触发的发育反应缺陷。与这些表型一致,DHR78突变体无法激活为变态做准备的第三龄中期调控层级。DHR78蛋白与许多受蜕皮甾体调控的胀泡位点结合,表明DHR78直接调控胀泡基因的表达。此外,DHR78的异位表达对发育没有影响,表明其活性在翻译后受到调控。我们提出,DHR78是一种配体激活受体,在引导果蝇变态的起始过程中发挥核心作用。

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