Cargando…

Ecdysone receptor isoforms play distinct roles in larval–pupal–adult transition in Leptinotarsa decemlineata

A heterodimer of two nuclear receptors, ecdysone receptor (EcR) and ultraspiracle, mediates 20‐hydroxyecdysone (20E) signaling to modulate many aspects in insect life, such as molting and metamorphosis, reproduction, diapause and innate immunity. In the present paper, we intended to determine the is...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Qing‐Yu, Deng, Pan, Zhang, Qiong, Li, Ang, Fu, Kai‐Yun, Guo, Wen‐Chao, Li, Guo‐Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277042/
https://www.ncbi.nlm.nih.gov/pubmed/30688001
http://dx.doi.org/10.1111/1744-7917.12662
_version_ 1783543035460583424
author Xu, Qing‐Yu
Deng, Pan
Zhang, Qiong
Li, Ang
Fu, Kai‐Yun
Guo, Wen‐Chao
Li, Guo‐Qing
author_facet Xu, Qing‐Yu
Deng, Pan
Zhang, Qiong
Li, Ang
Fu, Kai‐Yun
Guo, Wen‐Chao
Li, Guo‐Qing
author_sort Xu, Qing‐Yu
collection PubMed
description A heterodimer of two nuclear receptors, ecdysone receptor (EcR) and ultraspiracle, mediates 20‐hydroxyecdysone (20E) signaling to modulate many aspects in insect life, such as molting and metamorphosis, reproduction, diapause and innate immunity. In the present paper, we intended to determine the isoform‐specific roles of EcR during larval–pupal–adult transition in the Colorado potato beetle. Double‐stranded RNAs (dsRNAs) were prepared using the common (dsEcR) or isoform‐specific (dsEcRA, dsEcRB1) regions of EcR as templates. Ingestion of either dsEcR or dsEcRA, rather than dsEcRB1, by the penultimate (3rd) and final (4th) instar larvae caused failure of larval–pupal and pupal–adult ecdysis. The RNA interference (RNAi) larvae remained as prepupae, or became deformed pupae and adults. Determination of messenger RNA (mRNA) levels of EcR isoforms found that LdEcRA regulates the expression of LdEcRB1. Moreover, silencing the two EcR transcripts, LdEcRA or LdEcRB1 reduced the mRNA levels of Ldspo and Ldsad, and lowered 20E titer. In contrast, the expression levels of HR3, HR4, E74 and E75 were significantly decreased in the LdEcR or LdEcRA RNAi larvae, but not in LdEcRB1 depleted specimens. Dietary supplement with 20E did not restore the expression of five 20E signaling genes (USP, HR3, HR4, E74 and E75), and only partially alleviated the pupation defects in dsEcR‐ or dsEcRA‐fed beetles. These data suggest that EcR plays isoform‐specific roles in the regulation of ecdysteroidogenesis and the transduction of 20E signal in L. decemlineata.
format Online
Article
Text
id pubmed-7277042
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-72770422020-06-09 Ecdysone receptor isoforms play distinct roles in larval–pupal–adult transition in Leptinotarsa decemlineata Xu, Qing‐Yu Deng, Pan Zhang, Qiong Li, Ang Fu, Kai‐Yun Guo, Wen‐Chao Li, Guo‐Qing Insect Sci Original Articles A heterodimer of two nuclear receptors, ecdysone receptor (EcR) and ultraspiracle, mediates 20‐hydroxyecdysone (20E) signaling to modulate many aspects in insect life, such as molting and metamorphosis, reproduction, diapause and innate immunity. In the present paper, we intended to determine the isoform‐specific roles of EcR during larval–pupal–adult transition in the Colorado potato beetle. Double‐stranded RNAs (dsRNAs) were prepared using the common (dsEcR) or isoform‐specific (dsEcRA, dsEcRB1) regions of EcR as templates. Ingestion of either dsEcR or dsEcRA, rather than dsEcRB1, by the penultimate (3rd) and final (4th) instar larvae caused failure of larval–pupal and pupal–adult ecdysis. The RNA interference (RNAi) larvae remained as prepupae, or became deformed pupae and adults. Determination of messenger RNA (mRNA) levels of EcR isoforms found that LdEcRA regulates the expression of LdEcRB1. Moreover, silencing the two EcR transcripts, LdEcRA or LdEcRB1 reduced the mRNA levels of Ldspo and Ldsad, and lowered 20E titer. In contrast, the expression levels of HR3, HR4, E74 and E75 were significantly decreased in the LdEcR or LdEcRA RNAi larvae, but not in LdEcRB1 depleted specimens. Dietary supplement with 20E did not restore the expression of five 20E signaling genes (USP, HR3, HR4, E74 and E75), and only partially alleviated the pupation defects in dsEcR‐ or dsEcRA‐fed beetles. These data suggest that EcR plays isoform‐specific roles in the regulation of ecdysteroidogenesis and the transduction of 20E signal in L. decemlineata. John Wiley and Sons Inc. 2019-03-12 2020-06 /pmc/articles/PMC7277042/ /pubmed/30688001 http://dx.doi.org/10.1111/1744-7917.12662 Text en © 2019 The Authors. Insect Science published by John Wiley & Sons Australia, Ltd on behalf of Institute of Zoology, Chinese Academy of Sciences This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Xu, Qing‐Yu
Deng, Pan
Zhang, Qiong
Li, Ang
Fu, Kai‐Yun
Guo, Wen‐Chao
Li, Guo‐Qing
Ecdysone receptor isoforms play distinct roles in larval–pupal–adult transition in Leptinotarsa decemlineata
title Ecdysone receptor isoforms play distinct roles in larval–pupal–adult transition in Leptinotarsa decemlineata
title_full Ecdysone receptor isoforms play distinct roles in larval–pupal–adult transition in Leptinotarsa decemlineata
title_fullStr Ecdysone receptor isoforms play distinct roles in larval–pupal–adult transition in Leptinotarsa decemlineata
title_full_unstemmed Ecdysone receptor isoforms play distinct roles in larval–pupal–adult transition in Leptinotarsa decemlineata
title_short Ecdysone receptor isoforms play distinct roles in larval–pupal–adult transition in Leptinotarsa decemlineata
title_sort ecdysone receptor isoforms play distinct roles in larval–pupal–adult transition in leptinotarsa decemlineata
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277042/
https://www.ncbi.nlm.nih.gov/pubmed/30688001
http://dx.doi.org/10.1111/1744-7917.12662
work_keys_str_mv AT xuqingyu ecdysonereceptorisoformsplaydistinctrolesinlarvalpupaladulttransitioninleptinotarsadecemlineata
AT dengpan ecdysonereceptorisoformsplaydistinctrolesinlarvalpupaladulttransitioninleptinotarsadecemlineata
AT zhangqiong ecdysonereceptorisoformsplaydistinctrolesinlarvalpupaladulttransitioninleptinotarsadecemlineata
AT liang ecdysonereceptorisoformsplaydistinctrolesinlarvalpupaladulttransitioninleptinotarsadecemlineata
AT fukaiyun ecdysonereceptorisoformsplaydistinctrolesinlarvalpupaladulttransitioninleptinotarsadecemlineata
AT guowenchao ecdysonereceptorisoformsplaydistinctrolesinlarvalpupaladulttransitioninleptinotarsadecemlineata
AT liguoqing ecdysonereceptorisoformsplaydistinctrolesinlarvalpupaladulttransitioninleptinotarsadecemlineata