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果蝇蛹前期对蜕皮激素遗传反应阶段特异性的分子机制。

A molecular mechanism for the stage specificity of the Drosophila prepupal genetic response to ecdysone.

作者信息

Woodard C T, Baehrecke E H, Thummel C S

机构信息

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

出版信息

Cell. 1994 Nov 18;79(4):607-15. doi: 10.1016/0092-8674(94)90546-0.

Abstract

Two successive pulses of ecdysone signal the ends of larval and prepupal development in Drosophila, inducing early and late puffs in the salivary gland polytene chromosomes. Early puff induction in prepupae is dependent on a preceding period of protein synthesis and low ecdysone concentration. We demonstrate here that the competence acquired during this interval can be provided by beta FTZ-F1, a nuclear hormone receptor superfamily member derived from the 75CD mid-prepupal puff. We show that beta FTZ-F1 represses its own transcription and is repressed by ecdysone, explaining its brief expression in mid-prepupae. We further show that ectopic beta FTZ-F1 expression leads to enhanced levels of ecdysone-induced BR-C, E74, and E75 early gene transcription and premature induction of the stage-specific 93F early puff and E93 transcription. These findings indicate that beta FTZ-F1 plays a central role in the prepupal genetic response to ecdysone and provide a molecular mechanism for stage-specific responses to steroid hormones.

摘要

两次连续的蜕皮激素脉冲标志着果蝇幼虫和蛹前期发育的结束,诱导唾液腺多线染色体出现早期和晚期胀泡。蛹前期早期胀泡的诱导依赖于之前的蛋白质合成期和低浓度蜕皮激素。我们在此证明,在此期间获得的感受态可以由βFTZ-F1提供,βFTZ-F1是一种核激素受体超家族成员,源自蛹前期中期的75CD胀泡。我们表明,βFTZ-F1抑制其自身转录,并受到蜕皮激素的抑制,这解释了它在蛹前期中期的短暂表达。我们进一步表明,异位表达βFTZ-F1会导致蜕皮激素诱导的BR-C、E74和E75早期基因转录水平升高,以及阶段特异性的93F早期胀泡和E93转录的过早诱导。这些发现表明,βFTZ-F1在蛹前期对蜕皮激素的遗传反应中起核心作用,并为对类固醇激素的阶段特异性反应提供了一种分子机制。

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