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转录因子 E93 通过直接促进果蝇中的 Dpp 信号通路来调节翅膀发育。

Transcription factor E93 regulates wing development by directly promoting Dpp signaling in Drosophila.

机构信息

State Key Laboratory of Silkworm Genome Biology, Biological Science Research Center, Southwest University, Chongqing, 400715, China.

State Key Laboratory of Silkworm Genome Biology, Biological Science Research Center, Southwest University, Chongqing, 400715, China; Chongqing Key Laboratory of Sericultural Science, Chongqing Engineering and Technology Research Center for Novel Silk Materials, Southwest University, Chongqing, 400715, China.

出版信息

Biochem Biophys Res Commun. 2019 May 21;513(1):280-286. doi: 10.1016/j.bbrc.2019.03.100. Epub 2019 Apr 4.

DOI:10.1016/j.bbrc.2019.03.100
PMID:30954218
Abstract

Transcription factor E93 is a steroid hormone ecdysone early response gene and plays crucial roles in both the degradation of larval tissues and the formation of adult organs during insect metamorphosis with the prepupal-pupal-adult transition. However, the molecular mechanism underlying E93 regulation is poorly understood. In this study, we found that specific knockdown of the E93 gene in the Drosophila wing disrupted wing development. Analyzing ChIP-seq signals for E93 in Drosophila wing identified that the decapentaplegic (Dpp) gene was a potential downstream target of E93. ChIP-PCR analysis and dual-luciferase reporter assay confirmed that E93 could bind to the Dpp promoter and enhanced its activity. Furthermore, the expressions of Dpp and other components in the Dpp signaling pathway were upregulated following E93 overexpression in Drosophila S2 cells but were decreased after E93 knockdown in the wing. Moreover, the impairment of the Dpp signaling pathway phenocopied the defects of E93 knockdown on wing development. Taken together, our results suggest that E93 modulates the Dpp signaling pathway to regulate wing development during Drosophila metamorphosis.

摘要

转录因子 E93 是一种类固醇激素蜕皮激素早期反应基因,在昆虫变态过程中幼虫组织的降解和成虫器官的形成中起着至关重要的作用,伴随着预蛹-蛹-成虫的转变。然而,E93 调节的分子机制还知之甚少。在这项研究中,我们发现果蝇翅膀中 E93 基因的特异性敲低会破坏翅膀的发育。分析果蝇翅膀中 E93 的 ChIP-seq 信号表明,同源异形盒基因 decapentaplegic(Dpp)是 E93 的一个潜在下游靶标。ChIP-PCR 分析和双荧光素酶报告基因 assay 证实 E93 可以结合 Dpp 启动子并增强其活性。此外,在果蝇 S2 细胞中过表达 E93 会上调 Dpp 及其信号通路中其他成分的表达,但在翅膀中敲低 E93 后表达量下降。此外,Dpp 信号通路的损伤模拟了 E93 敲低对翅膀发育的缺陷。总之,我们的研究结果表明,E93 通过调节 Dpp 信号通路来调节果蝇变态过程中的翅膀发育。

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Transcription factor E93 regulates wing development by directly promoting Dpp signaling in Drosophila.转录因子 E93 通过直接促进果蝇中的 Dpp 信号通路来调节翅膀发育。
Biochem Biophys Res Commun. 2019 May 21;513(1):280-286. doi: 10.1016/j.bbrc.2019.03.100. Epub 2019 Apr 4.
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Drosophila E93 promotes adult development and suppresses larval responses to ecdysone during metamorphosis.果蝇E93促进成虫发育,并在变态过程中抑制幼虫对蜕皮激素的反应。
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Expression of E93 provides an instructive cue to control dynamic enhancer activity and chromatin accessibility during development.E93 的表达为控制发育过程中动态增强子活性和染色质可及性提供了一个有指导意义的线索。
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schnurri is required for dpp-dependent patterning of the Drosophila wing.Schnurri蛋白是果蝇翅膀中依赖于Dpp的模式形成所必需的。
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The Drosophila COMPASS-like Cmi-Trr coactivator complex regulates dpp/BMP signaling in pattern formation.果蝇 COMPASS 样 Cmi-Trr 共激活复合物在形态发生中调节 dpp/BMP 信号通路。
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The ecdysone receptor controls the post-critical weight switch to nutrition-independent differentiation in Drosophila wing imaginal discs.蜕皮激素受体控制果蝇翅成虫盘向营养非依赖型分化的关键体重转换。
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Dpp signaling inhibits proliferation in the Drosophila wing by Omb-dependent regional control of bantam.Dpp 信号通过 Omb 依赖的 bantam 的区域控制抑制果蝇翅膀的增殖。
Development. 2013 Jul;140(14):2917-22. doi: 10.1242/dev.094300.

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Drosophila E93 promotes adult development and suppresses larval responses to ecdysone during metamorphosis.果蝇E93促进成虫发育,并在变态过程中抑制幼虫对蜕皮激素的反应。
Dev Biol. 2022 Jan;481:104-115. doi: 10.1016/j.ydbio.2021.10.001. Epub 2021 Oct 11.
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Mechanisms underlying the control of dynamic regulatory element activity and chromatin accessibility during metamorphosis.
在变态过程中控制动态调控元件活性和染色质可及性的机制。
Curr Opin Insect Sci. 2021 Feb;43:21-28. doi: 10.1016/j.cois.2020.08.007. Epub 2020 Sep 23.