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FLP-1 neuropeptides modulate sensory and motor circuits in the nematode Caenorhabditis elegans

Parasitic nematodes infect over one quarter of the population worldwide, causing morbidity in over one billion people. Current anthelmintic drugs are beginning to lose effectiveness due to the presence of resistant strains. We are interested in the role of neuropeptides, which regulate behaviors in...

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Autores principales: Buntschuh, Ingrid, Raps, Daniel A., Joseph, Ivor, Reid, Christopher, Chait, Alexander, Totanes, Raubern, Sawh, Michelle, Li, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5749679/
https://www.ncbi.nlm.nih.gov/pubmed/29293515
http://dx.doi.org/10.1371/journal.pone.0189320
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author Buntschuh, Ingrid
Raps, Daniel A.
Joseph, Ivor
Reid, Christopher
Chait, Alexander
Totanes, Raubern
Sawh, Michelle
Li, Chris
author_facet Buntschuh, Ingrid
Raps, Daniel A.
Joseph, Ivor
Reid, Christopher
Chait, Alexander
Totanes, Raubern
Sawh, Michelle
Li, Chris
author_sort Buntschuh, Ingrid
collection PubMed
description Parasitic nematodes infect over one quarter of the population worldwide, causing morbidity in over one billion people. Current anthelmintic drugs are beginning to lose effectiveness due to the presence of resistant strains. We are interested in the role of neuropeptides, which regulate behaviors in all organisms, as another possible target for anthelmintic drugs. FMRFamide-related peptides (FaRPs) are a family of neuropeptides that are conserved throughout the animal kingdom. In particular, nematodes contain the largest family of FaRPs identified thus far and many of these FaRPs are identical among different nematode species; FaRPs in nematodes are collectively referred to as FLPs (FMRFamide-like peptides). However, little is known about the function of these FLPs. We are using the non-parasitic nematode Caenorhabditis elegans as a model for examining FLPs in nematodes. C. elegans contains at least 31 flp genes that encode 72 potential FLPs. Among the flp genes, flp-1 is one of the few that is universally found in nematodes. FLP-1 neuropeptides were previously reported to be involved in sensory and motor functions. However, previous alleles of flp-1 also disrupted a neighboring gene, daf-10. To understand the phenotypes of flp-1, new alleles that specifically disrupt flp-1 were characterized. The previously reported locomotory and egg-laying defects were found to be due to loss of flp-1, while the osmolarity defect is due to loss of daf-10. In addition, loss of flp-1 and daf-10 both cause several phenotypes that increase in severity in the double mutants by disrupting different neurons in the neural circuits.
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spelling pubmed-57496792018-01-26 FLP-1 neuropeptides modulate sensory and motor circuits in the nematode Caenorhabditis elegans Buntschuh, Ingrid Raps, Daniel A. Joseph, Ivor Reid, Christopher Chait, Alexander Totanes, Raubern Sawh, Michelle Li, Chris PLoS One Research Article Parasitic nematodes infect over one quarter of the population worldwide, causing morbidity in over one billion people. Current anthelmintic drugs are beginning to lose effectiveness due to the presence of resistant strains. We are interested in the role of neuropeptides, which regulate behaviors in all organisms, as another possible target for anthelmintic drugs. FMRFamide-related peptides (FaRPs) are a family of neuropeptides that are conserved throughout the animal kingdom. In particular, nematodes contain the largest family of FaRPs identified thus far and many of these FaRPs are identical among different nematode species; FaRPs in nematodes are collectively referred to as FLPs (FMRFamide-like peptides). However, little is known about the function of these FLPs. We are using the non-parasitic nematode Caenorhabditis elegans as a model for examining FLPs in nematodes. C. elegans contains at least 31 flp genes that encode 72 potential FLPs. Among the flp genes, flp-1 is one of the few that is universally found in nematodes. FLP-1 neuropeptides were previously reported to be involved in sensory and motor functions. However, previous alleles of flp-1 also disrupted a neighboring gene, daf-10. To understand the phenotypes of flp-1, new alleles that specifically disrupt flp-1 were characterized. The previously reported locomotory and egg-laying defects were found to be due to loss of flp-1, while the osmolarity defect is due to loss of daf-10. In addition, loss of flp-1 and daf-10 both cause several phenotypes that increase in severity in the double mutants by disrupting different neurons in the neural circuits. Public Library of Science 2018-01-02 /pmc/articles/PMC5749679/ /pubmed/29293515 http://dx.doi.org/10.1371/journal.pone.0189320 Text en © 2018 Buntschuh 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
Buntschuh, Ingrid
Raps, Daniel A.
Joseph, Ivor
Reid, Christopher
Chait, Alexander
Totanes, Raubern
Sawh, Michelle
Li, Chris
FLP-1 neuropeptides modulate sensory and motor circuits in the nematode Caenorhabditis elegans
title FLP-1 neuropeptides modulate sensory and motor circuits in the nematode Caenorhabditis elegans
title_full FLP-1 neuropeptides modulate sensory and motor circuits in the nematode Caenorhabditis elegans
title_fullStr FLP-1 neuropeptides modulate sensory and motor circuits in the nematode Caenorhabditis elegans
title_full_unstemmed FLP-1 neuropeptides modulate sensory and motor circuits in the nematode Caenorhabditis elegans
title_short FLP-1 neuropeptides modulate sensory and motor circuits in the nematode Caenorhabditis elegans
title_sort flp-1 neuropeptides modulate sensory and motor circuits in the nematode caenorhabditis elegans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5749679/
https://www.ncbi.nlm.nih.gov/pubmed/29293515
http://dx.doi.org/10.1371/journal.pone.0189320
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