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Urotensin II in Invertebrates: From Structure to Function in Aplysia californica

Neuropeptides are ancient signaling molecules that are involved in many aspects of organism homeostasis and function. Urotensin II (UII), a peptide with a range of hormonal functions, previously has been reported exclusively in vertebrates. Here, we provide the first direct evidence that UII-like pe...

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Autores principales: Romanova, Elena V., Sasaki, Kosei, Alexeeva, Vera, Vilim, Ferdinand S., Jing, Jian, Richmond, Timothy A., Weiss, Klaudiusz R., Sweedler, Jonathan V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493602/
https://www.ncbi.nlm.nih.gov/pubmed/23144960
http://dx.doi.org/10.1371/journal.pone.0048764
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author Romanova, Elena V.
Sasaki, Kosei
Alexeeva, Vera
Vilim, Ferdinand S.
Jing, Jian
Richmond, Timothy A.
Weiss, Klaudiusz R.
Sweedler, Jonathan V.
author_facet Romanova, Elena V.
Sasaki, Kosei
Alexeeva, Vera
Vilim, Ferdinand S.
Jing, Jian
Richmond, Timothy A.
Weiss, Klaudiusz R.
Sweedler, Jonathan V.
author_sort Romanova, Elena V.
collection PubMed
description Neuropeptides are ancient signaling molecules that are involved in many aspects of organism homeostasis and function. Urotensin II (UII), a peptide with a range of hormonal functions, previously has been reported exclusively in vertebrates. Here, we provide the first direct evidence that UII-like peptides are also present in an invertebrate, specifically, the marine mollusk Aplysia californica. The presence of UII in the central nervous system (CNS) of Aplysia implies a more ancient gene lineage than vertebrates. Using representational difference analysis, we identified an mRNA of a protein precursor that encodes a predicted neuropeptide, we named Aplysia urotensin II (apUII), with a sequence and structural similarity to vertebrate UII. With in-situ hybridization and immunohistochemistry, we mapped the expression of apUII mRNA and its prohormone in the CNS and localized apUII-like immunoreactivity to buccal sensory neurons and cerebral A-cluster neurons. Mass spectrometry performed on individual isolated neurons, and tandem mass spectrometry on fractionated peptide extracts, allowed us to define the posttranslational processing of the apUII neuropeptide precursor and confirm the highly conserved cyclic nature of the mature neuropeptide apUII. Electrophysiological analysis of the central effects of a synthetic apUII suggests it plays a role in satiety and/or aversive signaling in feeding behaviors. Finding the homologue of vertebrate UII in the numerically small CNS of an invertebrate animal model is important for gaining insights into the molecular mechanisms and pathways mediating the bioactivity of UII in the higher metazoan.
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spelling pubmed-34936022012-11-09 Urotensin II in Invertebrates: From Structure to Function in Aplysia californica Romanova, Elena V. Sasaki, Kosei Alexeeva, Vera Vilim, Ferdinand S. Jing, Jian Richmond, Timothy A. Weiss, Klaudiusz R. Sweedler, Jonathan V. PLoS One Research Article Neuropeptides are ancient signaling molecules that are involved in many aspects of organism homeostasis and function. Urotensin II (UII), a peptide with a range of hormonal functions, previously has been reported exclusively in vertebrates. Here, we provide the first direct evidence that UII-like peptides are also present in an invertebrate, specifically, the marine mollusk Aplysia californica. The presence of UII in the central nervous system (CNS) of Aplysia implies a more ancient gene lineage than vertebrates. Using representational difference analysis, we identified an mRNA of a protein precursor that encodes a predicted neuropeptide, we named Aplysia urotensin II (apUII), with a sequence and structural similarity to vertebrate UII. With in-situ hybridization and immunohistochemistry, we mapped the expression of apUII mRNA and its prohormone in the CNS and localized apUII-like immunoreactivity to buccal sensory neurons and cerebral A-cluster neurons. Mass spectrometry performed on individual isolated neurons, and tandem mass spectrometry on fractionated peptide extracts, allowed us to define the posttranslational processing of the apUII neuropeptide precursor and confirm the highly conserved cyclic nature of the mature neuropeptide apUII. Electrophysiological analysis of the central effects of a synthetic apUII suggests it plays a role in satiety and/or aversive signaling in feeding behaviors. Finding the homologue of vertebrate UII in the numerically small CNS of an invertebrate animal model is important for gaining insights into the molecular mechanisms and pathways mediating the bioactivity of UII in the higher metazoan. Public Library of Science 2012-11-08 /pmc/articles/PMC3493602/ /pubmed/23144960 http://dx.doi.org/10.1371/journal.pone.0048764 Text en © 2012 Romanova 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Romanova, Elena V.
Sasaki, Kosei
Alexeeva, Vera
Vilim, Ferdinand S.
Jing, Jian
Richmond, Timothy A.
Weiss, Klaudiusz R.
Sweedler, Jonathan V.
Urotensin II in Invertebrates: From Structure to Function in Aplysia californica
title Urotensin II in Invertebrates: From Structure to Function in Aplysia californica
title_full Urotensin II in Invertebrates: From Structure to Function in Aplysia californica
title_fullStr Urotensin II in Invertebrates: From Structure to Function in Aplysia californica
title_full_unstemmed Urotensin II in Invertebrates: From Structure to Function in Aplysia californica
title_short Urotensin II in Invertebrates: From Structure to Function in Aplysia californica
title_sort urotensin ii in invertebrates: from structure to function in aplysia californica
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493602/
https://www.ncbi.nlm.nih.gov/pubmed/23144960
http://dx.doi.org/10.1371/journal.pone.0048764
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