幼激素通过Kr-h1/Dnmt2介导的Acp65A启动子的DNA甲基化抑制黑腹果蝇成虫角质层的形成。

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Qianyu He, Xiaochun Fan, Shunxin Wang, Shanshan Chen, Jinxia Chen
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引用次数: 0

摘要

黑腹果蝇的想象表皮细胞分化形成成年角质层发生在大约40-93 h。蛹蜕皮时给予的幼激素(JH)会在腹部形成第二个蛹角质层,而不是成虫角质层。尽管成人角质层基因Acp65A已被报道在JH治疗后下调,但其调节机制尚不清楚。在这里,我们发现JH初级反应基因Krüppel同源物1(Kr-h1)通过JH作用在抑制成人角质层形成中发挥着至关重要的作用。Kr-h1的过表达模拟了敲低Kr-h1,减弱了JH对成人腹部角质层形成的抑制作用。此外,我们发现Kr-h1通过直接结合Acp65A启动子区内的共有Kr-h1结合位点(KBS)来抑制Acp65A的转录。此外,DNA甲基转移酶Dnmt2显示与Kr-h1相互作用,与KBS结合以促进KBS周围序列的DNA甲基化,进而抑制Acp65A的转录。本研究加深了我们对JH对果蝇成虫变态“现状”作用的分子基础的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Juvenile hormone inhibits adult cuticle formation in Drosophila melanogaster through Kr-h1/Dnmt2-mediated DNA methylation of Acp65A promoter

Juvenile hormone inhibits adult cuticle formation in Drosophila melanogaster through Kr-h1/Dnmt2-mediated DNA methylation of Acp65A promoter

Juvenile hormone inhibits adult cuticle formation in Drosophila melanogaster through Kr-h1/Dnmt2-mediated DNA methylation of Acp65A promoter

Differentiation of imaginal epidermal cells of Drosophila melanogaster to form adult cuticles occurs at approximately 40–93 h after puparium formation. Juvenile hormone (JH) given at pupariation results in formation of a second pupal cuticle in the abdomen instead of the adult cuticle. Although the adult cuticle gene Acp65A has been reported to be down-regulated following JH treatment, the regulatory mechanism remains unclear. Here, we found that the JH primary response gene Krüppel homologue 1 (Kr-h1) plays a vital role in the repression of adult cuticle formation through the mediation of JH action. Overexpression of Kr-h1 mimicked—while knocking down of Kr-h1 attenuated—the inhibitory action of JH on the formation of the adult abdominal cuticle. Further, we found that Kr-h1 inhibited the transcription of Acp65A by directly binding to the consensus Kr-h1 binding site (KBS) within the Acp65A promoter region. Moreover, the DNA methyltransferase Dnmt2 was shown to interact with Kr-h1, combined with the KBS to promote the DNA methylation of sequences around the KBS, in turn inhibiting the transcription of Acp65A. This study advances our understanding of the molecular basis of the “status quo” action of JH on the Drosophila adult metamorphosis.

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来源期刊
Insect Molecular Biology
Insect Molecular Biology 生物-昆虫学
CiteScore
4.80
自引率
3.80%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Insect Molecular Biology has been dedicated to providing researchers with the opportunity to publish high quality original research on topics broadly related to insect molecular biology since 1992. IMB is particularly interested in publishing research in insect genomics/genes and proteomics/proteins. This includes research related to: • insect gene structure • control of gene expression • localisation and function/activity of proteins • interactions of proteins and ligands/substrates • effect of mutations on gene/protein function • evolution of insect genes/genomes, especially where principles relevant to insects in general are established • molecular population genetics where data are used to identify genes (or regions of genomes) involved in specific adaptations • gene mapping using molecular tools • molecular interactions of insects with microorganisms including Wolbachia, symbionts and viruses or other pathogens transmitted by insects Papers can include large data sets e.g.from micro-array or proteomic experiments or analyses of genome sequences done in silico (subject to the data being placed in the context of hypothesis testing).
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