The miRNA-mRNA modules enhance juvenile hormone biosynthesis for insect vitellogenesis and egg production.

IF 2.9 1区 农林科学 Q1 ENTOMOLOGY
Wanwan Li, Mingzhi Liu, Zitong Zhuang, Lulu Gao, Jiasheng Song, Shutang Zhou
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引用次数: 0

Abstract

In addition to preventing precocious larval metamorphosis, juvenile hormone (JH), synthesized in corpora allata (CA), is known to stimulate female reproduction of insects. JH titer is extremely low or absent during metamorphosis, but thereafter rapidly increases in the previtellogenic stage and rises to a peak in the vitellogenic phase. However, the mechanisms underlying the biosynthesis of high levels of JH in adults remain unclear. We found in this study that 12 genes involved in JH synthesis pathway were highly expressed in the CA of adult locusts. By transcriptome analysis and quantitative real-time - polymerase chain reaction validation, a total of 106 evolutionary conserved micro RNAs (miRNAs) and 163 species-specific miRNAs were identified in locust CA. Dual-luciferase assay revealed that 17 miRNAs bound to 10 JH synthesis genes (JHSGs) and downregulated their expression. These miRNAs were expressed in low levels during vitellogenic stage, which was oppositive from that of targeting JHSGs. Six miRNAs including miR-971-3p, miR-31a, miR-9-5p, miR-1-3p, miR-315, and miR-282 were selected for function study. Co-application of agomiRs resulted in significantly decreased levels of targeting JHSGs, accompanied by significantly reduced vitellogenin expression as well as arrested ovarian development. The data suggest that multiple miRNAs expressed synchronously at low levels in the vitellogenic phase, thereby ensuring the high levels of JHSG expression to facilitate JH biosynthesis required for JH-dependent female reproduction. The findings provide important information for deciphering miRNA-messenger RNA modules for JH biosynthesis as well as JH regulation of insect metamorphosis and reproduction.

miRNA-mRNA 模块增强了昆虫卵黄发生和产卵过程中幼年激素的生物合成。
除了防止幼虫早熟变态外,在异形体(CA)中合成的幼虫激素(JH)还能刺激昆虫的雌性繁殖。JH 滴度在变态过程中极低或没有,但在卵黄形成前期迅速增加,并在卵黄形成期达到峰值。然而,成虫体内高水平 JH 的生物合成机制仍不清楚。本研究发现,参与JH合成途径的12个基因在成年蝗虫的CA中高表达。通过转录组分析和实时定量聚合酶链反应验证,在蝗虫CA中发现了106个进化保守的微RNA(miRNA)和163个物种特异性miRNA。双荧光素酶测定显示,17 个 miRNA 与 10 个 JH 合成基因(JHSGs)结合并下调其表达。这些 miRNA 在卵黄形成期的表达水平较低,与靶向 JHSGs 的表达水平相反。包括 miR-971-3p、miR-31a、miR-9-5p、miR-1-3p、miR-315 和 miR-282 在内的六种 miRNA 被选中进行功能研究。联合应用agomiRs会导致靶向JHSGs的水平显著下降,同时卵黄素的表达也会显著降低,卵巢发育也会停止。这些数据表明,在卵黄发生期,多个 miRNAs 以低水平同步表达,从而确保了 JHSG 的高水平表达,以促进 JH 依赖性雌性繁殖所需的 JH 生物合成。这些发现为破译 JH 生物合成的 miRNA-信使 RNA 模块以及 JH 对昆虫变态和繁殖的调控提供了重要信息。
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 Science
Insect Science 生物-昆虫学
CiteScore
7.80
自引率
5.00%
发文量
1379
审稿时长
6.0 months
期刊介绍: Insect Science is an English-language journal, which publishes original research articles dealing with all fields of research in into insects and other terrestrial arthropods. Papers in any of the following fields will be considered: ecology, behavior, biogeography, physiology, biochemistry, sociobiology, phylogeny, pest management, and exotic incursions. The emphasis of the journal is on the adaptation and evolutionary biology of insects from the molecular to the ecosystem level. Reviews, mini reviews and letters to the editor, book reviews, and information about academic activities of the society are also published.
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