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Dop1 enhances conspecific olfactory attraction by inhibiting miR-9a maturation in locusts
Dopamine receptor 1 (Dop1) mediates locust attraction behaviors, however, the mechanism by which Dop1 modulates this process remains unknown to date. Here, we identify differentially expressed small RNAs associated with locust olfactory attraction after activating and inhibiting Dop1. Small RNA tran...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864846/ https://www.ncbi.nlm.nih.gov/pubmed/29567955 http://dx.doi.org/10.1038/s41467-018-03437-z |
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author | Guo, Xiaojiao Ma, Zongyuan Du, Baozhen Li, Ting Li, Wudi Xu, Lingling He, Jing Kang, Le |
author_facet | Guo, Xiaojiao Ma, Zongyuan Du, Baozhen Li, Ting Li, Wudi Xu, Lingling He, Jing Kang, Le |
author_sort | Guo, Xiaojiao |
collection | PubMed |
description | Dopamine receptor 1 (Dop1) mediates locust attraction behaviors, however, the mechanism by which Dop1 modulates this process remains unknown to date. Here, we identify differentially expressed small RNAs associated with locust olfactory attraction after activating and inhibiting Dop1. Small RNA transcriptome analysis and qPCR validation reveal that Dop1 activation and inhibition downregulates and upregulates microRNA-9a (miR-9a) expression, respectively. miR-9a knockdown in solitarious locusts increases their attraction to gregarious volatiles, whereas miR-9a overexpression in gregarious locusts reduces olfactory attraction. Moreover, miR-9a directly targets adenylyl cyclase 2 (ac2), causing its downregulation at the mRNA and protein levels. ac2 responds to Dop1 and mediates locust olfactory attraction. Mechanistically, Dop1 inhibits miR-9a expression through inducing the dissociation of La protein from pre-miR-9a and resulting in miR-9a maturation inhibition. Our results reveal a Dop1–miR-9a–AC2 circuit that modulates locust olfactory attraction underlying aggregation. This study suggests that miRNAs act as key messengers in the GPCR signaling. |
format | Online Article Text |
id | pubmed-5864846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58648462018-03-28 Dop1 enhances conspecific olfactory attraction by inhibiting miR-9a maturation in locusts Guo, Xiaojiao Ma, Zongyuan Du, Baozhen Li, Ting Li, Wudi Xu, Lingling He, Jing Kang, Le Nat Commun Article Dopamine receptor 1 (Dop1) mediates locust attraction behaviors, however, the mechanism by which Dop1 modulates this process remains unknown to date. Here, we identify differentially expressed small RNAs associated with locust olfactory attraction after activating and inhibiting Dop1. Small RNA transcriptome analysis and qPCR validation reveal that Dop1 activation and inhibition downregulates and upregulates microRNA-9a (miR-9a) expression, respectively. miR-9a knockdown in solitarious locusts increases their attraction to gregarious volatiles, whereas miR-9a overexpression in gregarious locusts reduces olfactory attraction. Moreover, miR-9a directly targets adenylyl cyclase 2 (ac2), causing its downregulation at the mRNA and protein levels. ac2 responds to Dop1 and mediates locust olfactory attraction. Mechanistically, Dop1 inhibits miR-9a expression through inducing the dissociation of La protein from pre-miR-9a and resulting in miR-9a maturation inhibition. Our results reveal a Dop1–miR-9a–AC2 circuit that modulates locust olfactory attraction underlying aggregation. This study suggests that miRNAs act as key messengers in the GPCR signaling. Nature Publishing Group UK 2018-03-22 /pmc/articles/PMC5864846/ /pubmed/29567955 http://dx.doi.org/10.1038/s41467-018-03437-z Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Guo, Xiaojiao Ma, Zongyuan Du, Baozhen Li, Ting Li, Wudi Xu, Lingling He, Jing Kang, Le Dop1 enhances conspecific olfactory attraction by inhibiting miR-9a maturation in locusts |
title | Dop1 enhances conspecific olfactory attraction by inhibiting miR-9a maturation in locusts |
title_full | Dop1 enhances conspecific olfactory attraction by inhibiting miR-9a maturation in locusts |
title_fullStr | Dop1 enhances conspecific olfactory attraction by inhibiting miR-9a maturation in locusts |
title_full_unstemmed | Dop1 enhances conspecific olfactory attraction by inhibiting miR-9a maturation in locusts |
title_short | Dop1 enhances conspecific olfactory attraction by inhibiting miR-9a maturation in locusts |
title_sort | dop1 enhances conspecific olfactory attraction by inhibiting mir-9a maturation in locusts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864846/ https://www.ncbi.nlm.nih.gov/pubmed/29567955 http://dx.doi.org/10.1038/s41467-018-03437-z |
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