Cargando…

miR-31-5p regulates cold acclimation of the wood-boring beetle Monochamus alternatus via ascaroside signaling

BACKGROUND: Survival to cold stress in insects living in temperate environments requires the deployment of strategies that lead to physiological changes involved in freeze tolerance or freeze avoidance. These strategies may consist of, for instance, the induction of metabolic depression, accumulatio...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Bin, Zhao, Lilin, Ning, Jing, Wickham, Jacob D., Tian, Haokai, Zhang, Xiaoming, Yang, Meiling, Wang, Xiangming, Sun, Jianghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697373/
https://www.ncbi.nlm.nih.gov/pubmed/33246464
http://dx.doi.org/10.1186/s12915-020-00926-w
_version_ 1783615591951630336
author Zhang, Bin
Zhao, Lilin
Ning, Jing
Wickham, Jacob D.
Tian, Haokai
Zhang, Xiaoming
Yang, Meiling
Wang, Xiangming
Sun, Jianghua
author_facet Zhang, Bin
Zhao, Lilin
Ning, Jing
Wickham, Jacob D.
Tian, Haokai
Zhang, Xiaoming
Yang, Meiling
Wang, Xiangming
Sun, Jianghua
author_sort Zhang, Bin
collection PubMed
description BACKGROUND: Survival to cold stress in insects living in temperate environments requires the deployment of strategies that lead to physiological changes involved in freeze tolerance or freeze avoidance. These strategies may consist of, for instance, the induction of metabolic depression, accumulation of cryoprotectants, or the production of antifreeze proteins, however, little is known about the way such mechanisms are regulated and the signals involved in their activation. Ascarosides are signaling molecules usually known to regulate nematode behavior and development, whose expression was recently found to relate to thermal plasticity in the Japanese pine sawyer beetle Monochamus alternatus. Accumulating evidence also points to miRNAs as another class of regulators differentially expressed in response to cold stress, which are predicted to target genes involved in cold adaptation of insects. Here, we demonstrate a novel pathway involved in insect cold acclimation, through miRNA-mediated regulation of ascaroside function. RESULTS: We initially discovered that experimental cold acclimation can enhance the beetle’s cold hardiness. Through screening and functional verification, we found miR-31-5p, upregulated under cold stress, significantly contributes to this enhancement. Mechanistically, miR-31-5p promotes production of an ascaroside (asc-C9) in the beetle by negatively targeting the rate-limiting enzyme, acyl-CoA oxidase in peroxisomal β-oxidation cycles. Feeding experiments with synthetic asc-C9 suggests it may serve as a signal to promote cold acclimation through metabolic depression and accumulation of cryoprotectants with specific gene expression patterns. CONCLUSIONS: Our results point to important roles of miRNA-mediated regulation of ascaroside function in insect cold adaptation. This enhanced cold tolerance may allow higher survival of M. alternatus in winter and be pivotal in shaping its wide distribution range, greatly expanding the threat of pine wilt disease, and thus can also inspire the development of ascaroside-based pest management strategies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-020-00926-w.
format Online
Article
Text
id pubmed-7697373
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-76973732020-11-30 miR-31-5p regulates cold acclimation of the wood-boring beetle Monochamus alternatus via ascaroside signaling Zhang, Bin Zhao, Lilin Ning, Jing Wickham, Jacob D. Tian, Haokai Zhang, Xiaoming Yang, Meiling Wang, Xiangming Sun, Jianghua BMC Biol Research Article BACKGROUND: Survival to cold stress in insects living in temperate environments requires the deployment of strategies that lead to physiological changes involved in freeze tolerance or freeze avoidance. These strategies may consist of, for instance, the induction of metabolic depression, accumulation of cryoprotectants, or the production of antifreeze proteins, however, little is known about the way such mechanisms are regulated and the signals involved in their activation. Ascarosides are signaling molecules usually known to regulate nematode behavior and development, whose expression was recently found to relate to thermal plasticity in the Japanese pine sawyer beetle Monochamus alternatus. Accumulating evidence also points to miRNAs as another class of regulators differentially expressed in response to cold stress, which are predicted to target genes involved in cold adaptation of insects. Here, we demonstrate a novel pathway involved in insect cold acclimation, through miRNA-mediated regulation of ascaroside function. RESULTS: We initially discovered that experimental cold acclimation can enhance the beetle’s cold hardiness. Through screening and functional verification, we found miR-31-5p, upregulated under cold stress, significantly contributes to this enhancement. Mechanistically, miR-31-5p promotes production of an ascaroside (asc-C9) in the beetle by negatively targeting the rate-limiting enzyme, acyl-CoA oxidase in peroxisomal β-oxidation cycles. Feeding experiments with synthetic asc-C9 suggests it may serve as a signal to promote cold acclimation through metabolic depression and accumulation of cryoprotectants with specific gene expression patterns. CONCLUSIONS: Our results point to important roles of miRNA-mediated regulation of ascaroside function in insect cold adaptation. This enhanced cold tolerance may allow higher survival of M. alternatus in winter and be pivotal in shaping its wide distribution range, greatly expanding the threat of pine wilt disease, and thus can also inspire the development of ascaroside-based pest management strategies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-020-00926-w. BioMed Central 2020-11-27 /pmc/articles/PMC7697373/ /pubmed/33246464 http://dx.doi.org/10.1186/s12915-020-00926-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Zhang, Bin
Zhao, Lilin
Ning, Jing
Wickham, Jacob D.
Tian, Haokai
Zhang, Xiaoming
Yang, Meiling
Wang, Xiangming
Sun, Jianghua
miR-31-5p regulates cold acclimation of the wood-boring beetle Monochamus alternatus via ascaroside signaling
title miR-31-5p regulates cold acclimation of the wood-boring beetle Monochamus alternatus via ascaroside signaling
title_full miR-31-5p regulates cold acclimation of the wood-boring beetle Monochamus alternatus via ascaroside signaling
title_fullStr miR-31-5p regulates cold acclimation of the wood-boring beetle Monochamus alternatus via ascaroside signaling
title_full_unstemmed miR-31-5p regulates cold acclimation of the wood-boring beetle Monochamus alternatus via ascaroside signaling
title_short miR-31-5p regulates cold acclimation of the wood-boring beetle Monochamus alternatus via ascaroside signaling
title_sort mir-31-5p regulates cold acclimation of the wood-boring beetle monochamus alternatus via ascaroside signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697373/
https://www.ncbi.nlm.nih.gov/pubmed/33246464
http://dx.doi.org/10.1186/s12915-020-00926-w
work_keys_str_mv AT zhangbin mir315pregulatescoldacclimationofthewoodboringbeetlemonochamusalternatusviaascarosidesignaling
AT zhaolilin mir315pregulatescoldacclimationofthewoodboringbeetlemonochamusalternatusviaascarosidesignaling
AT ningjing mir315pregulatescoldacclimationofthewoodboringbeetlemonochamusalternatusviaascarosidesignaling
AT wickhamjacobd mir315pregulatescoldacclimationofthewoodboringbeetlemonochamusalternatusviaascarosidesignaling
AT tianhaokai mir315pregulatescoldacclimationofthewoodboringbeetlemonochamusalternatusviaascarosidesignaling
AT zhangxiaoming mir315pregulatescoldacclimationofthewoodboringbeetlemonochamusalternatusviaascarosidesignaling
AT yangmeiling mir315pregulatescoldacclimationofthewoodboringbeetlemonochamusalternatusviaascarosidesignaling
AT wangxiangming mir315pregulatescoldacclimationofthewoodboringbeetlemonochamusalternatusviaascarosidesignaling
AT sunjianghua mir315pregulatescoldacclimationofthewoodboringbeetlemonochamusalternatusviaascarosidesignaling