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微小 RNA-277 调控多巴脱羧酶控制棉铃虫的幼虫-蛹和蛹-成虫变态。

MicroRNA-277 regulates dopa decarboxylase to control larval-pupal and pupal-adult metamorphosis of Helicoverpa armigera.

机构信息

Department of Entomology, MOA Key Laboratory of Pest Monitoring and Green Management, College of Plant Protection, China Agricultural University, Beijing, 100193, China.

Department of Entomology, Pennsylvania State University, University Park, PA, 16802, USA.

出版信息

Insect Biochem Mol Biol. 2020 Jul;122:103391. doi: 10.1016/j.ibmb.2020.103391. Epub 2020 Apr 30.

DOI:10.1016/j.ibmb.2020.103391
PMID:32360955
Abstract

Insect metamorphosis is a complex process involving many metabolic pathways, such as juvenile hormones and molting hormones, bioamines, microRNAs (miRNAs), etc. However, relatively little is known about the biogenic amines and their miRNAs to regulate cotton bollworm metamorphosis. Here we show that one miRNA, miR-277 regulates larval-pupal and pupal-adult metamorphosis of cotton bollworm by targeting the 3'UTR of Dopa decarboxylase (DDC), a synthetic catalytic enzyme of dopamine. Injection of miR-277 agomir inhibited the expression of DDC at the mRNA and protein levels, leading to defects in the pupation and emergence of H. armigera that was consistent with the phenotype obtained by injection of DDC double-stranded RNA (dsRNA). Injection of miR-277 antagomir induced the mRNA and protein expression of DDC and rescued the phenotype of pupation failure caused by DDC gene silencing. Unexpectedly, miR-277 antagomir can also cause failure of emergence of H. armigera and both agomir and antagomir of miR-277 injection could cause abnormal phenotypes in wing veins. This study reveals that elaborate regulation of miRNA and its target gene expression is prerequisite for insect development, which provides a new insight to study the developmental mechanisms of insect wing veins.

摘要

昆虫变态是一个涉及许多代谢途径的复杂过程,如保幼激素和蜕皮激素、生物胺、微小 RNA(miRNA)等。然而,关于生物胺及其 miRNA 如何调节棉铃虫变态的研究相对较少。在这里,我们发现一个 miRNA,miR-277 通过靶向多巴胺脱羧酶(DDC)的 3'UTR 来调节棉铃虫的幼虫-蛹和蛹-成虫变态,DDC 是多巴胺的合成催化酶。miR-277 agomir 的注射抑制了 DDC 在 mRNA 和蛋白质水平的表达,导致 H. armigera 的化蛹和羽化缺陷,与注射 DDC 双链 RNA(dsRNA)获得的表型一致。miR-277 antagomir 的注射诱导了 DDC 的 mRNA 和蛋白质表达,并挽救了 DDC 基因沉默引起的化蛹失败表型。出乎意料的是,miR-277 antagomir 也会导致 H. armigera 的羽化失败,miR-277 的 agomir 和 antagomir 注射都能导致翅脉异常表型。这项研究揭示了 miRNA 及其靶基因表达的精细调控是昆虫发育的前提,为研究昆虫翅脉的发育机制提供了新的见解。

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