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A new neuropeptide insect parathyroid hormone iPTH in the red flour beetle Tribolium castaneum

In the postgenomics era, comparative genomics have advanced the understanding of evolutionary processes of neuropeptidergic signaling systems. The evolutionary origin of many neuropeptidergic signaling systems can be traced date back to early metazoan evolution based on the conserved sequences. Inse...

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Autores principales: Xie, Jia, Sang, Ming, Song, Xiaowen, Zhang, Sisi, Kim, Donghun, Veenstra, Jan A., Park, Yoonseong, Li, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224569/
https://www.ncbi.nlm.nih.gov/pubmed/32365064
http://dx.doi.org/10.1371/journal.pgen.1008772
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author Xie, Jia
Sang, Ming
Song, Xiaowen
Zhang, Sisi
Kim, Donghun
Veenstra, Jan A.
Park, Yoonseong
Li, Bin
author_facet Xie, Jia
Sang, Ming
Song, Xiaowen
Zhang, Sisi
Kim, Donghun
Veenstra, Jan A.
Park, Yoonseong
Li, Bin
author_sort Xie, Jia
collection PubMed
description In the postgenomics era, comparative genomics have advanced the understanding of evolutionary processes of neuropeptidergic signaling systems. The evolutionary origin of many neuropeptidergic signaling systems can be traced date back to early metazoan evolution based on the conserved sequences. Insect parathyroid hormone receptor (iPTHR) was previously described as an ortholog of vertebrate PTHR that has a well-known function in controlling bone remodeling. However, there was no sequence homologous to PTH sequence in insect genomes, leaving the iPTHR as an orphan receptor. Here, we identified the authentic ligand insect PTH (iPTH) for the iPTHR. The taxonomic distribution of iPTHR, which is lacking in Diptera and Lepidoptera, provided a lead for identifying the authentic ligand. We found that a previously described orphan ligand known as PXXXamide (where X is any amino acid) described in the cuttlefish Sepia officinalis has a similar taxonomic distribution pattern as iPTHR. Tests of this peptide, iPTH, in functional reporter assays confirmed the interaction of the ligand-receptor pair. Study of a model beetle, Tribolium castaneum, was used to investigate the function of the iPTH signaling system by RNA interference followed by RNA sequencing and phenotyping. The results suggested that the iPTH system is likely involved in the regulation of cuticle formation that culminates with a phenotype of defects in wing exoskeleton maturation at the time of adult eclosion. Moreover, RNAi of iPTHRs also led to significant reductions in egg numbers and hatching rates after parental RNAi.
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spelling pubmed-72245692020-06-01 A new neuropeptide insect parathyroid hormone iPTH in the red flour beetle Tribolium castaneum Xie, Jia Sang, Ming Song, Xiaowen Zhang, Sisi Kim, Donghun Veenstra, Jan A. Park, Yoonseong Li, Bin PLoS Genet Research Article In the postgenomics era, comparative genomics have advanced the understanding of evolutionary processes of neuropeptidergic signaling systems. The evolutionary origin of many neuropeptidergic signaling systems can be traced date back to early metazoan evolution based on the conserved sequences. Insect parathyroid hormone receptor (iPTHR) was previously described as an ortholog of vertebrate PTHR that has a well-known function in controlling bone remodeling. However, there was no sequence homologous to PTH sequence in insect genomes, leaving the iPTHR as an orphan receptor. Here, we identified the authentic ligand insect PTH (iPTH) for the iPTHR. The taxonomic distribution of iPTHR, which is lacking in Diptera and Lepidoptera, provided a lead for identifying the authentic ligand. We found that a previously described orphan ligand known as PXXXamide (where X is any amino acid) described in the cuttlefish Sepia officinalis has a similar taxonomic distribution pattern as iPTHR. Tests of this peptide, iPTH, in functional reporter assays confirmed the interaction of the ligand-receptor pair. Study of a model beetle, Tribolium castaneum, was used to investigate the function of the iPTH signaling system by RNA interference followed by RNA sequencing and phenotyping. The results suggested that the iPTH system is likely involved in the regulation of cuticle formation that culminates with a phenotype of defects in wing exoskeleton maturation at the time of adult eclosion. Moreover, RNAi of iPTHRs also led to significant reductions in egg numbers and hatching rates after parental RNAi. Public Library of Science 2020-05-04 /pmc/articles/PMC7224569/ /pubmed/32365064 http://dx.doi.org/10.1371/journal.pgen.1008772 Text en © 2020 Xie 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
Xie, Jia
Sang, Ming
Song, Xiaowen
Zhang, Sisi
Kim, Donghun
Veenstra, Jan A.
Park, Yoonseong
Li, Bin
A new neuropeptide insect parathyroid hormone iPTH in the red flour beetle Tribolium castaneum
title A new neuropeptide insect parathyroid hormone iPTH in the red flour beetle Tribolium castaneum
title_full A new neuropeptide insect parathyroid hormone iPTH in the red flour beetle Tribolium castaneum
title_fullStr A new neuropeptide insect parathyroid hormone iPTH in the red flour beetle Tribolium castaneum
title_full_unstemmed A new neuropeptide insect parathyroid hormone iPTH in the red flour beetle Tribolium castaneum
title_short A new neuropeptide insect parathyroid hormone iPTH in the red flour beetle Tribolium castaneum
title_sort new neuropeptide insect parathyroid hormone ipth in the red flour beetle tribolium castaneum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224569/
https://www.ncbi.nlm.nih.gov/pubmed/32365064
http://dx.doi.org/10.1371/journal.pgen.1008772
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