Cargando…
CREB-B acts as a key mediator of NPF/NO pathway involved in phase-related locomotor plasticity in locusts
Gene expression changes in neural systems are essential for environment-induced behavioral plasticity in animals; however, neuronal signaling pathways mediating the effect of external stimuli on transcriptional changes are largely unknown. Recently, we have demonstrated that the neuropeptide F (NPF)...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6561586/ https://www.ncbi.nlm.nih.gov/pubmed/31150381 http://dx.doi.org/10.1371/journal.pgen.1008176 |
_version_ | 1783426156755681280 |
---|---|
author | Hou, Li Li, Beibei Ding, Ding Kang, Le Wang, Xianhui |
author_facet | Hou, Li Li, Beibei Ding, Ding Kang, Le Wang, Xianhui |
author_sort | Hou, Li |
collection | PubMed |
description | Gene expression changes in neural systems are essential for environment-induced behavioral plasticity in animals; however, neuronal signaling pathways mediating the effect of external stimuli on transcriptional changes are largely unknown. Recently, we have demonstrated that the neuropeptide F (NPF)/nitric oxide (NO) signaling pathway plays a regulatory role in phase-related locomotor plasticity in the migratory locust, Locusta migratoria. Here, we report that a conserved transcription factor, cAMP response element-binding protein B (CREB-B), is a key mediator involved in the signaling pathway from NPF2 to NOS in the migratory locust, triggering locomotor activity shift between solitarious and gregarious phases. We find that CREB-B directly activates brain NOS expression by interacting with NOS promoter region. The phosphorylation at serine 110 site of CREB-B dynamically changes in response to population density variation and is negatively controlled by NPF2. The involvement of CREB-B in NPF2-regulated locomotor plasticity is further validated by RNAi experiment and behavioral assay. Furthermore, we reveal that protein kinase A mediates the regulatory effects of NPF2 on CREB-B phosphorylation and NOS transcription. These findings highlight a precise signal cascade underlying environment-induced behavioral plasticity. |
format | Online Article Text |
id | pubmed-6561586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-65615862019-06-20 CREB-B acts as a key mediator of NPF/NO pathway involved in phase-related locomotor plasticity in locusts Hou, Li Li, Beibei Ding, Ding Kang, Le Wang, Xianhui PLoS Genet Research Article Gene expression changes in neural systems are essential for environment-induced behavioral plasticity in animals; however, neuronal signaling pathways mediating the effect of external stimuli on transcriptional changes are largely unknown. Recently, we have demonstrated that the neuropeptide F (NPF)/nitric oxide (NO) signaling pathway plays a regulatory role in phase-related locomotor plasticity in the migratory locust, Locusta migratoria. Here, we report that a conserved transcription factor, cAMP response element-binding protein B (CREB-B), is a key mediator involved in the signaling pathway from NPF2 to NOS in the migratory locust, triggering locomotor activity shift between solitarious and gregarious phases. We find that CREB-B directly activates brain NOS expression by interacting with NOS promoter region. The phosphorylation at serine 110 site of CREB-B dynamically changes in response to population density variation and is negatively controlled by NPF2. The involvement of CREB-B in NPF2-regulated locomotor plasticity is further validated by RNAi experiment and behavioral assay. Furthermore, we reveal that protein kinase A mediates the regulatory effects of NPF2 on CREB-B phosphorylation and NOS transcription. These findings highlight a precise signal cascade underlying environment-induced behavioral plasticity. Public Library of Science 2019-05-31 /pmc/articles/PMC6561586/ /pubmed/31150381 http://dx.doi.org/10.1371/journal.pgen.1008176 Text en © 2019 Hou et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Hou, Li Li, Beibei Ding, Ding Kang, Le Wang, Xianhui CREB-B acts as a key mediator of NPF/NO pathway involved in phase-related locomotor plasticity in locusts |
title | CREB-B acts as a key mediator of NPF/NO pathway involved in phase-related locomotor plasticity in locusts |
title_full | CREB-B acts as a key mediator of NPF/NO pathway involved in phase-related locomotor plasticity in locusts |
title_fullStr | CREB-B acts as a key mediator of NPF/NO pathway involved in phase-related locomotor plasticity in locusts |
title_full_unstemmed | CREB-B acts as a key mediator of NPF/NO pathway involved in phase-related locomotor plasticity in locusts |
title_short | CREB-B acts as a key mediator of NPF/NO pathway involved in phase-related locomotor plasticity in locusts |
title_sort | creb-b acts as a key mediator of npf/no pathway involved in phase-related locomotor plasticity in locusts |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6561586/ https://www.ncbi.nlm.nih.gov/pubmed/31150381 http://dx.doi.org/10.1371/journal.pgen.1008176 |
work_keys_str_mv | AT houli crebbactsasakeymediatorofnpfnopathwayinvolvedinphaserelatedlocomotorplasticityinlocusts AT libeibei crebbactsasakeymediatorofnpfnopathwayinvolvedinphaserelatedlocomotorplasticityinlocusts AT dingding crebbactsasakeymediatorofnpfnopathwayinvolvedinphaserelatedlocomotorplasticityinlocusts AT kangle crebbactsasakeymediatorofnpfnopathwayinvolvedinphaserelatedlocomotorplasticityinlocusts AT wangxianhui crebbactsasakeymediatorofnpfnopathwayinvolvedinphaserelatedlocomotorplasticityinlocusts |