PBX and Dfd cooperatively regulate stage-specific expression of 30 K protein BmLP1 in Bombyx mori.

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Qingqing Linghu, Haoyun Li, Jiahui Wan, Xiaolu Zhang, Jingjing Huang, Zhiqing Li, Yuying Wang, Jianhua Xia, Zhaoming Dong, Ying Lin, Ping Zhao, Yan Zhang
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引用次数: 0

Abstract

Nutrient accumulation is essential for insect metamorphosis. As a group of important nutrient-storage proteins, forty-six 30 K proteins (30KPs), including BmLP1-BmLP46, have been identified in the silkworm, Bombyx mori. Most 30KPs are synthesised in the last instar larvae, and the stage-specific expression of 30KPs is believed to be regulated by juvenile hormone (JH)-dependent pathways; however, the specific regulatory mechanism remains unclear. In this study, we found that a 30KP gene Bmlp1 was expressed after Day 3 of the fifth instar, and its expression was down-regulated by JH analogue. We also identified a cis-response element (CRE) on the promoter of Bmlp1. Dfd was determined to bind to this CRE adjacent to another CRE that serves as a binding site for PBX. Dfd is a HOX transcription factor found to exhibit an expression pattern similar to that of PBX. The interaction between PBX and Dfd was confirmed using bimolecular fluorescence complementation and GST pull-down experiments. The expression of Bmlp1 was down-regulated when PBX and Dfd were overexpressed in BmN cells, whereas it was up-regulated when PBX and Dfd were knocked down in BmN cells. Our data show that the transcription factor Dfd, and the cofactor PBX, synergistically regulate the transcription of Bmlp1 in B. mori. This study provides a reference for an in-depth understanding of the regulation of insect development mediated by JH.

PBX和Dfd共同调控家蚕30k蛋白BmLP1的分期特异性表达。
营养物质的积累是昆虫变态的必要条件。家蚕30k蛋白(30KPs)是一类重要的营养储存蛋白,目前已在家蚕中鉴定出46种30KPs,其中包括BmLP1-BmLP46。大多数30KPs在末龄幼虫中合成,30KPs的阶段特异性表达被认为是由幼虫激素(JH)依赖性途径调节的;然而,具体的监管机制尚不清楚。在本研究中,我们发现30KP基因Bmlp1在第5龄第3天表达,其表达被JH类似物下调。我们还在Bmlp1的启动子上发现了一个顺式反应元件(CRE)。确定Dfd与相邻的CRE结合,该CRE作为PBX的结合位点。Dfd是一种HOX转录因子,其表达模式与PBX相似。通过双分子荧光互补和GST下拉实验证实了PBX和Dfd之间的相互作用。BmN细胞中PBX和Dfd过表达时,Bmlp1表达下调,BmN细胞中PBX和Dfd过表达时,Bmlp1表达上调。我们的数据表明,转录因子Dfd和辅因子PBX协同调节家蚕Bmlp1的转录。本研究为深入了解JH介导的昆虫发育调控提供了参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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