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CORL Expression and Function in Insulin Producing Neurons Reversibly Influences Adult Longevity in Drosophila
CORL proteins (known as SKOR in mice, Fussel in humans and fussel in Flybase) are a family of CNS specific proteins related to Sno/Ski oncogenes. Their developmental and adult roles are largely unknown. A Drosophila CORL (dCORL) reporter gene is expressed in all Drosophila insulin-like peptide 2 (dI...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Genetics Society of America
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6118311/ https://www.ncbi.nlm.nih.gov/pubmed/30006413 http://dx.doi.org/10.1534/g3.118.200572 |
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author | Tran, Nancy L. Goldsmith, Samuel L. Dimitriadou, Agapi Takaesu, Norma T. Consoulas, Christos Newfeld, Stuart J. |
author_facet | Tran, Nancy L. Goldsmith, Samuel L. Dimitriadou, Agapi Takaesu, Norma T. Consoulas, Christos Newfeld, Stuart J. |
author_sort | Tran, Nancy L. |
collection | PubMed |
description | CORL proteins (known as SKOR in mice, Fussel in humans and fussel in Flybase) are a family of CNS specific proteins related to Sno/Ski oncogenes. Their developmental and adult roles are largely unknown. A Drosophila CORL (dCORL) reporter gene is expressed in all Drosophila insulin-like peptide 2 (dILP2) neurons of the pars intercerebralis (PI) of the larval and adult brain. The transcription factor Drifter is also expressed in the PI in a subset of dCORL and dILP2 expressing neurons and in several non-dILP2 neurons. dCORL mutant virgin adult brains are missing all dILP2 neurons that do not also express Drifter. This phenotype is also seen when expressing dCORL-RNAi in neurosecretory cells of the PI. dCORL mutant virgin adults of both sexes have a significantly shorter lifespan than their parental strain. This longevity defect is completely reversed by mating (lifespan increases over 50% for males and females). Analyses of dCORL mutant mated adult brains revealed a complete rescue of dILP2 neurons without Drifter. Taken together, the data suggest that dCORL participates in a neural network connecting the insulin signaling pathway, longevity and mating. The conserved sequence and CNS specificity of all CORL proteins imply that this network may be operating in mammals. |
format | Online Article Text |
id | pubmed-6118311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-61183112018-09-04 CORL Expression and Function in Insulin Producing Neurons Reversibly Influences Adult Longevity in Drosophila Tran, Nancy L. Goldsmith, Samuel L. Dimitriadou, Agapi Takaesu, Norma T. Consoulas, Christos Newfeld, Stuart J. G3 (Bethesda) Investigations CORL proteins (known as SKOR in mice, Fussel in humans and fussel in Flybase) are a family of CNS specific proteins related to Sno/Ski oncogenes. Their developmental and adult roles are largely unknown. A Drosophila CORL (dCORL) reporter gene is expressed in all Drosophila insulin-like peptide 2 (dILP2) neurons of the pars intercerebralis (PI) of the larval and adult brain. The transcription factor Drifter is also expressed in the PI in a subset of dCORL and dILP2 expressing neurons and in several non-dILP2 neurons. dCORL mutant virgin adult brains are missing all dILP2 neurons that do not also express Drifter. This phenotype is also seen when expressing dCORL-RNAi in neurosecretory cells of the PI. dCORL mutant virgin adults of both sexes have a significantly shorter lifespan than their parental strain. This longevity defect is completely reversed by mating (lifespan increases over 50% for males and females). Analyses of dCORL mutant mated adult brains revealed a complete rescue of dILP2 neurons without Drifter. Taken together, the data suggest that dCORL participates in a neural network connecting the insulin signaling pathway, longevity and mating. The conserved sequence and CNS specificity of all CORL proteins imply that this network may be operating in mammals. Genetics Society of America 2018-07-13 /pmc/articles/PMC6118311/ /pubmed/30006413 http://dx.doi.org/10.1534/g3.118.200572 Text en Copyright © 2018 Tran et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigations Tran, Nancy L. Goldsmith, Samuel L. Dimitriadou, Agapi Takaesu, Norma T. Consoulas, Christos Newfeld, Stuart J. CORL Expression and Function in Insulin Producing Neurons Reversibly Influences Adult Longevity in Drosophila |
title | CORL Expression and Function in Insulin Producing Neurons Reversibly Influences Adult Longevity in Drosophila |
title_full | CORL Expression and Function in Insulin Producing Neurons Reversibly Influences Adult Longevity in Drosophila |
title_fullStr | CORL Expression and Function in Insulin Producing Neurons Reversibly Influences Adult Longevity in Drosophila |
title_full_unstemmed | CORL Expression and Function in Insulin Producing Neurons Reversibly Influences Adult Longevity in Drosophila |
title_short | CORL Expression and Function in Insulin Producing Neurons Reversibly Influences Adult Longevity in Drosophila |
title_sort | corl expression and function in insulin producing neurons reversibly influences adult longevity in drosophila |
topic | Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6118311/ https://www.ncbi.nlm.nih.gov/pubmed/30006413 http://dx.doi.org/10.1534/g3.118.200572 |
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