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Molecular cloning and characterization of the allatotropin precursor and receptor in the desert locust, Schistocerca gregaria

Allatotropins (ATs) are pleiotropic neuropeptides initially isolated from the tobacco hornworm, Manduca sexta. In 2008, the first receptor for AT-like peptides (ATR) was characterized in Bombyx mori. Since then, ATRs have also been characterized in M. sexta, Tribolium castaneum, Aedes aegypti and Bo...

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Autores principales: Lismont, Els, Vleugels, Rut, Marchal, Elisabeth, Badisco, Liesbeth, Van Wielendaele, Pieter, Lenaerts, Cynthia, Zels, Sven, Tobe, Stephen S., Vanden Broeck, Jozef, Verlinden, Heleen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357254/
https://www.ncbi.nlm.nih.gov/pubmed/25814925
http://dx.doi.org/10.3389/fnins.2015.00084
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author Lismont, Els
Vleugels, Rut
Marchal, Elisabeth
Badisco, Liesbeth
Van Wielendaele, Pieter
Lenaerts, Cynthia
Zels, Sven
Tobe, Stephen S.
Vanden Broeck, Jozef
Verlinden, Heleen
author_facet Lismont, Els
Vleugels, Rut
Marchal, Elisabeth
Badisco, Liesbeth
Van Wielendaele, Pieter
Lenaerts, Cynthia
Zels, Sven
Tobe, Stephen S.
Vanden Broeck, Jozef
Verlinden, Heleen
author_sort Lismont, Els
collection PubMed
description Allatotropins (ATs) are pleiotropic neuropeptides initially isolated from the tobacco hornworm, Manduca sexta. In 2008, the first receptor for AT-like peptides (ATR) was characterized in Bombyx mori. Since then, ATRs have also been characterized in M. sexta, Tribolium castaneum, Aedes aegypti and Bombus terrestris. These receptors show sequence similarity to vertebrate orexin (ORX) receptors. When generating an EST-database of the desert locust (Schistocerca gregaria) central nervous system, we found cDNA sequences encoding the Schgr-AT precursor and a fragment of its putative receptor. This receptor cDNA has now been completed and functionally expressed in mammalian cell lines. Activation of this receptor, designated as Schgr-ATR, by Schgr-AT caused an increase in intracellular calcium ions, as well as cyclic AMP (cAMP), with an EC(50) value in the nanomolar range. In addition, the transcript distribution of both the Schgr-AT precursor and Schgr-ATR was investigated by means of quantitative real-time PCR. Moreover, we found more evidence for the myotropic and allatostimulatory actions of Schgr-AT in the desert locust. These data are discussed and situated in a broader context by comparison with literature data on AT and ATR in insects.
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spelling pubmed-43572542015-03-26 Molecular cloning and characterization of the allatotropin precursor and receptor in the desert locust, Schistocerca gregaria Lismont, Els Vleugels, Rut Marchal, Elisabeth Badisco, Liesbeth Van Wielendaele, Pieter Lenaerts, Cynthia Zels, Sven Tobe, Stephen S. Vanden Broeck, Jozef Verlinden, Heleen Front Neurosci Endocrinology Allatotropins (ATs) are pleiotropic neuropeptides initially isolated from the tobacco hornworm, Manduca sexta. In 2008, the first receptor for AT-like peptides (ATR) was characterized in Bombyx mori. Since then, ATRs have also been characterized in M. sexta, Tribolium castaneum, Aedes aegypti and Bombus terrestris. These receptors show sequence similarity to vertebrate orexin (ORX) receptors. When generating an EST-database of the desert locust (Schistocerca gregaria) central nervous system, we found cDNA sequences encoding the Schgr-AT precursor and a fragment of its putative receptor. This receptor cDNA has now been completed and functionally expressed in mammalian cell lines. Activation of this receptor, designated as Schgr-ATR, by Schgr-AT caused an increase in intracellular calcium ions, as well as cyclic AMP (cAMP), with an EC(50) value in the nanomolar range. In addition, the transcript distribution of both the Schgr-AT precursor and Schgr-ATR was investigated by means of quantitative real-time PCR. Moreover, we found more evidence for the myotropic and allatostimulatory actions of Schgr-AT in the desert locust. These data are discussed and situated in a broader context by comparison with literature data on AT and ATR in insects. Frontiers Media S.A. 2015-03-12 /pmc/articles/PMC4357254/ /pubmed/25814925 http://dx.doi.org/10.3389/fnins.2015.00084 Text en Copyright © 2015 Lismont, Vleugels, Marchal, Badisco, Van Wielendaele, Lenaerts, Zels, Tobe, Vanden Broeck and Verlinden. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Lismont, Els
Vleugels, Rut
Marchal, Elisabeth
Badisco, Liesbeth
Van Wielendaele, Pieter
Lenaerts, Cynthia
Zels, Sven
Tobe, Stephen S.
Vanden Broeck, Jozef
Verlinden, Heleen
Molecular cloning and characterization of the allatotropin precursor and receptor in the desert locust, Schistocerca gregaria
title Molecular cloning and characterization of the allatotropin precursor and receptor in the desert locust, Schistocerca gregaria
title_full Molecular cloning and characterization of the allatotropin precursor and receptor in the desert locust, Schistocerca gregaria
title_fullStr Molecular cloning and characterization of the allatotropin precursor and receptor in the desert locust, Schistocerca gregaria
title_full_unstemmed Molecular cloning and characterization of the allatotropin precursor and receptor in the desert locust, Schistocerca gregaria
title_short Molecular cloning and characterization of the allatotropin precursor and receptor in the desert locust, Schistocerca gregaria
title_sort molecular cloning and characterization of the allatotropin precursor and receptor in the desert locust, schistocerca gregaria
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357254/
https://www.ncbi.nlm.nih.gov/pubmed/25814925
http://dx.doi.org/10.3389/fnins.2015.00084
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