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A small cohort of FRU(M) and Engrailed-expressing neurons mediate successful copulation in Drosophila melanogaster
BACKGROUND: In Drosophila, male flies require the expression of the male-specific Fruitless protein (FRU(M)) within the developing pupal and adult nervous system in order to produce male courtship and copulation behaviors. Recent evidence has shown that specific subsets of FRU(M) neurons are necessa...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664081/ https://www.ncbi.nlm.nih.gov/pubmed/23688386 http://dx.doi.org/10.1186/1471-2202-14-57 |
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author | Latham, Kristin L Liu, Ying-Show Taylor, Barbara J |
author_facet | Latham, Kristin L Liu, Ying-Show Taylor, Barbara J |
author_sort | Latham, Kristin L |
collection | PubMed |
description | BACKGROUND: In Drosophila, male flies require the expression of the male-specific Fruitless protein (FRU(M)) within the developing pupal and adult nervous system in order to produce male courtship and copulation behaviors. Recent evidence has shown that specific subsets of FRU(M) neurons are necessary for particular steps of courtship and copulation. In these neurons, FRU(M) function has been shown to be important for determining sex-specific neuronal characteristics, such as neurotransmitter profile and morphology. RESULTS: We identified a small cohort of FRU(M) interneurons in the brain and ventral nerve cord by their co-expression with the transcription factor Engrailed (En). We used an En-GAL4 driver to express a fru(M) RNAi construct in order to selectively deplete FRU(M) in these En/FRU(M) co-expressing neurons. In courtship and copulation tests, these males performed male courtship at wild-type levels but were frequently sterile. Sterility was a behavioral phenotype as these En-fru(M)RNAi males were less able to convert a copulation attempt into a stable copulation, or did not maintain copulation for long enough to transfer sperm and/or seminal fluid. CONCLUSIONS: We have identified a population of interneurons necessary for successful copulation in Drosophila. These data confirm a model in which subsets of FRU(M) neurons participate in independent neuronal circuits necessary for individual steps of male behavior. In addition, we have determined that these neurons in wild-type males have homologues in females and fru mutants, with similar placement, projection patterns, and neurochemical profiles. |
format | Online Article Text |
id | pubmed-3664081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36640812013-05-26 A small cohort of FRU(M) and Engrailed-expressing neurons mediate successful copulation in Drosophila melanogaster Latham, Kristin L Liu, Ying-Show Taylor, Barbara J BMC Neurosci Research Article BACKGROUND: In Drosophila, male flies require the expression of the male-specific Fruitless protein (FRU(M)) within the developing pupal and adult nervous system in order to produce male courtship and copulation behaviors. Recent evidence has shown that specific subsets of FRU(M) neurons are necessary for particular steps of courtship and copulation. In these neurons, FRU(M) function has been shown to be important for determining sex-specific neuronal characteristics, such as neurotransmitter profile and morphology. RESULTS: We identified a small cohort of FRU(M) interneurons in the brain and ventral nerve cord by their co-expression with the transcription factor Engrailed (En). We used an En-GAL4 driver to express a fru(M) RNAi construct in order to selectively deplete FRU(M) in these En/FRU(M) co-expressing neurons. In courtship and copulation tests, these males performed male courtship at wild-type levels but were frequently sterile. Sterility was a behavioral phenotype as these En-fru(M)RNAi males were less able to convert a copulation attempt into a stable copulation, or did not maintain copulation for long enough to transfer sperm and/or seminal fluid. CONCLUSIONS: We have identified a population of interneurons necessary for successful copulation in Drosophila. These data confirm a model in which subsets of FRU(M) neurons participate in independent neuronal circuits necessary for individual steps of male behavior. In addition, we have determined that these neurons in wild-type males have homologues in females and fru mutants, with similar placement, projection patterns, and neurochemical profiles. BioMed Central 2013-05-21 /pmc/articles/PMC3664081/ /pubmed/23688386 http://dx.doi.org/10.1186/1471-2202-14-57 Text en Copyright © 2013 Latham et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Latham, Kristin L Liu, Ying-Show Taylor, Barbara J A small cohort of FRU(M) and Engrailed-expressing neurons mediate successful copulation in Drosophila melanogaster |
title | A small cohort of FRU(M) and Engrailed-expressing neurons mediate successful copulation in Drosophila melanogaster |
title_full | A small cohort of FRU(M) and Engrailed-expressing neurons mediate successful copulation in Drosophila melanogaster |
title_fullStr | A small cohort of FRU(M) and Engrailed-expressing neurons mediate successful copulation in Drosophila melanogaster |
title_full_unstemmed | A small cohort of FRU(M) and Engrailed-expressing neurons mediate successful copulation in Drosophila melanogaster |
title_short | A small cohort of FRU(M) and Engrailed-expressing neurons mediate successful copulation in Drosophila melanogaster |
title_sort | small cohort of fru(m) and engrailed-expressing neurons mediate successful copulation in drosophila melanogaster |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664081/ https://www.ncbi.nlm.nih.gov/pubmed/23688386 http://dx.doi.org/10.1186/1471-2202-14-57 |
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