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Article: Functional evolution of Thyrotropin-releasing hormone neuropeptides: insights from an echinoderm

TitleFunctional evolution of Thyrotropin-releasing hormone neuropeptides: insights from an echinoderm
Authors
Issue Date9-Nov-2024
PublisherKunming Institute of Zoology, Chinese Academy of Sciences
Citation
Zoological Research, 2024 How to Cite?
Abstract

Feeding behavior is regulated by a rich network of endogenous neuropeptides. In chordates, this role is suggested to be under the control of diverse factors including the Thyrotropin-releasing hormone (TRH). It is unclear, however, whether this regulatory activity of TRH is functionally conserved in non-chordate metazoans, and to what extent this process is underpinned by interactions of TRH with other neuropeptides such as Cholecystokinin (CCK, known as a satiety signal). Here, we investigated the function and pathway of the TRH signaling system in the echinoderm Apostichopus japonicus. Combining bioinformatic analyses and ligand binding assay, we identified a functional receptor (AjTRHR) of TRH peptides, activating the signaling via MAPK/ERK1/2 pathways. Next, experimental TRH administration showed a significant feeding activity decrease and the up-regulation of CCK. Further RNA inference (RNAi) experiment confirmed that CCK and TRH are both involved in satiety signals mediating feeding inhibition. Evolutionary analysis of TRH-type peptides revealed that the short-isoform TRH is more conserved compared to the long-isoform, probably driven by strong selection acting on the functional redundancy. These novel findings provide evidence of a TRH system in a non-chordate deuterostome, expanding our understanding of the peptidergic signaling-mediate feeding regulation mechanism in marine invertebrates.


Persistent Identifierhttp://hdl.handle.net/10722/351232
ISSN
2023 Impact Factor: 4.0
2023 SCImago Journal Rankings: 1.286
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZheng, Yingqiu-
dc.contributor.authorLiu, Huachen-
dc.contributor.authorDang, Xin-
dc.contributor.authorGaitán-Espitia, Juan-
dc.contributor.authorChen, Muyan-
dc.date.accessioned2024-11-14T00:35:52Z-
dc.date.available2024-11-14T00:35:52Z-
dc.date.issued2024-11-09-
dc.identifier.citationZoological Research, 2024-
dc.identifier.issn2095-8137-
dc.identifier.urihttp://hdl.handle.net/10722/351232-
dc.description.abstract<p>Feeding behavior is regulated by a rich network of endogenous neuropeptides. In chordates, this role is suggested to be under the control of diverse factors including the Thyrotropin-releasing hormone (TRH). It is unclear, however, whether this regulatory activity of TRH is functionally conserved in non-chordate metazoans, and to what extent this process is underpinned by interactions of TRH with other neuropeptides such as Cholecystokinin (CCK, known as a satiety signal). Here, we investigated the function and pathway of the TRH signaling system in the echinoderm Apostichopus japonicus. Combining bioinformatic analyses and ligand binding assay, we identified a functional receptor (AjTRHR) of TRH peptides, activating the signaling via MAPK/ERK1/2 pathways. Next, experimental TRH administration showed a significant feeding activity decrease and the up-regulation of CCK. Further RNA inference (RNAi) experiment confirmed that CCK and TRH are both involved in satiety signals mediating feeding inhibition. Evolutionary analysis of TRH-type peptides revealed that the short-isoform TRH is more conserved compared to the long-isoform, probably driven by strong selection acting on the functional redundancy. These novel findings provide evidence of a TRH system in a non-chordate deuterostome, expanding our understanding of the peptidergic signaling-mediate feeding regulation mechanism in marine invertebrates.</p>-
dc.languageeng-
dc.publisherKunming Institute of Zoology, Chinese Academy of Sciences-
dc.relation.ispartofZoological Research-
dc.titleFunctional evolution of Thyrotropin-releasing hormone neuropeptides: insights from an echinoderm-
dc.typeArticle-
dc.identifier.doi10.24272/j.issn.2095-8137.2024.256-
dc.identifier.eissn2095-8137-
dc.identifier.isiWOS:001408425500018-
dc.identifier.issnl2095-8137-

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