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CCHamide-2 Is an Orexigenic Brain-Gut Peptide in Drosophila
The neuroendocrine peptides CCHamide-1 and -2, encoded by the genes ccha1 and -2, are produced by endocrine cells in the midgut and by neurons in the brain of Drosophila melanogaster. Here, we used the CRISPR/Cas9 technique to disrupt the ccha1 and -2 genes and identify mutant phenotypes with a focu...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500396/ https://www.ncbi.nlm.nih.gov/pubmed/26168160 http://dx.doi.org/10.1371/journal.pone.0133017 |
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author | Ren, Guilin R. Hauser, Frank Rewitz, Kim F. Kondo, Shu Engelbrecht, Alexander F. Didriksen, Anders K. Schjøtt, Suzanne R. Sembach, Frederikke E. Li, Shizhong Søgaard, Karen C. Søndergaard, Leif Grimmelikhuijzen, Cornelis J. P. |
author_facet | Ren, Guilin R. Hauser, Frank Rewitz, Kim F. Kondo, Shu Engelbrecht, Alexander F. Didriksen, Anders K. Schjøtt, Suzanne R. Sembach, Frederikke E. Li, Shizhong Søgaard, Karen C. Søndergaard, Leif Grimmelikhuijzen, Cornelis J. P. |
author_sort | Ren, Guilin R. |
collection | PubMed |
description | The neuroendocrine peptides CCHamide-1 and -2, encoded by the genes ccha1 and -2, are produced by endocrine cells in the midgut and by neurons in the brain of Drosophila melanogaster. Here, we used the CRISPR/Cas9 technique to disrupt the ccha1 and -2 genes and identify mutant phenotypes with a focus on ccha-2 mutants. We found that both larval and adult ccha2 mutants showed a significantly reduced food intake as measured in adult flies by the Capillary Feeding (CAFE) assay (up to 72% reduced food intake compared to wild-type). Locomotion tests in adult flies showed that ccha2 mutants had a significantly reduced locomotor activity especially around 8 a.m. and 8 p.m., where adult Drosophila normally feeds (up to 70% reduced locomotor activity compared to wild-type). Reduced larval feeding is normally coupled to a delayed larval development, a process that is mediated by insulin. Accordingly, we found that the ccha2 mutants had a remarkably delayed development, showing pupariation 70 hours after the pupariation time point of the wild-type. In contrast, the ccha-1 mutants were not developmentally delayed. We also found that the ccha2 mutants had up to 80% reduced mRNA concentrations coding for the Drosophila insulin-like-peptides-2 and -3, while these concentrations were unchanged for the ccha1 mutants. From these experiments we conclude that CCHamide-2 is an orexigenic peptide and an important factor for controlling developmental timing in Drosophila. |
format | Online Article Text |
id | pubmed-4500396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45003962015-07-17 CCHamide-2 Is an Orexigenic Brain-Gut Peptide in Drosophila Ren, Guilin R. Hauser, Frank Rewitz, Kim F. Kondo, Shu Engelbrecht, Alexander F. Didriksen, Anders K. Schjøtt, Suzanne R. Sembach, Frederikke E. Li, Shizhong Søgaard, Karen C. Søndergaard, Leif Grimmelikhuijzen, Cornelis J. P. PLoS One Research Article The neuroendocrine peptides CCHamide-1 and -2, encoded by the genes ccha1 and -2, are produced by endocrine cells in the midgut and by neurons in the brain of Drosophila melanogaster. Here, we used the CRISPR/Cas9 technique to disrupt the ccha1 and -2 genes and identify mutant phenotypes with a focus on ccha-2 mutants. We found that both larval and adult ccha2 mutants showed a significantly reduced food intake as measured in adult flies by the Capillary Feeding (CAFE) assay (up to 72% reduced food intake compared to wild-type). Locomotion tests in adult flies showed that ccha2 mutants had a significantly reduced locomotor activity especially around 8 a.m. and 8 p.m., where adult Drosophila normally feeds (up to 70% reduced locomotor activity compared to wild-type). Reduced larval feeding is normally coupled to a delayed larval development, a process that is mediated by insulin. Accordingly, we found that the ccha2 mutants had a remarkably delayed development, showing pupariation 70 hours after the pupariation time point of the wild-type. In contrast, the ccha-1 mutants were not developmentally delayed. We also found that the ccha2 mutants had up to 80% reduced mRNA concentrations coding for the Drosophila insulin-like-peptides-2 and -3, while these concentrations were unchanged for the ccha1 mutants. From these experiments we conclude that CCHamide-2 is an orexigenic peptide and an important factor for controlling developmental timing in Drosophila. Public Library of Science 2015-07-13 /pmc/articles/PMC4500396/ /pubmed/26168160 http://dx.doi.org/10.1371/journal.pone.0133017 Text en © 2015 Ren 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 Ren, Guilin R. Hauser, Frank Rewitz, Kim F. Kondo, Shu Engelbrecht, Alexander F. Didriksen, Anders K. Schjøtt, Suzanne R. Sembach, Frederikke E. Li, Shizhong Søgaard, Karen C. Søndergaard, Leif Grimmelikhuijzen, Cornelis J. P. CCHamide-2 Is an Orexigenic Brain-Gut Peptide in Drosophila |
title | CCHamide-2 Is an Orexigenic Brain-Gut Peptide in Drosophila
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title_full | CCHamide-2 Is an Orexigenic Brain-Gut Peptide in Drosophila
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title_fullStr | CCHamide-2 Is an Orexigenic Brain-Gut Peptide in Drosophila
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title_full_unstemmed | CCHamide-2 Is an Orexigenic Brain-Gut Peptide in Drosophila
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title_short | CCHamide-2 Is an Orexigenic Brain-Gut Peptide in Drosophila
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title_sort | cchamide-2 is an orexigenic brain-gut peptide in drosophila |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500396/ https://www.ncbi.nlm.nih.gov/pubmed/26168160 http://dx.doi.org/10.1371/journal.pone.0133017 |
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