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Mating disrupts morning anticipation in Drosophila melanogaster females

After mating, the physiology of Drosophila females undergo several important changes, some of which are reflected in their rest-activity cycles. To explore the hypothesis that mating modifies the temporal organization of locomotor activity patterns, we recorded fly activity by a video tracking metho...

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Autores principales: Riva, Sabrina, Ispizua, Juan Ignacio, Breide, María Trinidad, Polcowñuk, Sofía, Lobera, José Ricardo, Ceriani, María Fernanda, Risau-Gusman, Sebastian, Franco, Diana Lorena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9779042/
https://www.ncbi.nlm.nih.gov/pubmed/36548223
http://dx.doi.org/10.1371/journal.pgen.1010258
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author Riva, Sabrina
Ispizua, Juan Ignacio
Breide, María Trinidad
Polcowñuk, Sofía
Lobera, José Ricardo
Ceriani, María Fernanda
Risau-Gusman, Sebastian
Franco, Diana Lorena
author_facet Riva, Sabrina
Ispizua, Juan Ignacio
Breide, María Trinidad
Polcowñuk, Sofía
Lobera, José Ricardo
Ceriani, María Fernanda
Risau-Gusman, Sebastian
Franco, Diana Lorena
author_sort Riva, Sabrina
collection PubMed
description After mating, the physiology of Drosophila females undergo several important changes, some of which are reflected in their rest-activity cycles. To explore the hypothesis that mating modifies the temporal organization of locomotor activity patterns, we recorded fly activity by a video tracking method. Monitoring rest-activity patterns under light/dark (LD) cycles indicated that mated females lose their ability to anticipate the night-day transition, in stark contrast to males and virgins. This postmating response is mediated by the activation of the sex peptide receptor (SPR) mainly on pickpocket (ppk) expressing neurons, since reducing expression of this receptor in these neurons restores the ability to anticipate the LD transition in mated females. Furthermore, we provide evidence of connectivity between ppk+ neurons and the pigment-dispersing factor (PDF)-positive ventral lateral neurons (sLNv), which play a central role in the temporal organization of daily activity. Since PDF has been associated to the generation of the morning activity peak, we hypothesized that the mating signal could modulate PDF levels. Indeed, we confirm that mated females have reduced PDF levels at the dorsal protocerebrum; moreover, SPR downregulation in ppk+ neurons mimics PDF levels observed in males. In sum, our results are consistent with a model whereby mating-triggered signals reach clock neurons in the fly central nervous system to modulate the temporal organization of circadian behavior according to the needs of the new status.
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spelling pubmed-97790422022-12-23 Mating disrupts morning anticipation in Drosophila melanogaster females Riva, Sabrina Ispizua, Juan Ignacio Breide, María Trinidad Polcowñuk, Sofía Lobera, José Ricardo Ceriani, María Fernanda Risau-Gusman, Sebastian Franco, Diana Lorena PLoS Genet Research Article After mating, the physiology of Drosophila females undergo several important changes, some of which are reflected in their rest-activity cycles. To explore the hypothesis that mating modifies the temporal organization of locomotor activity patterns, we recorded fly activity by a video tracking method. Monitoring rest-activity patterns under light/dark (LD) cycles indicated that mated females lose their ability to anticipate the night-day transition, in stark contrast to males and virgins. This postmating response is mediated by the activation of the sex peptide receptor (SPR) mainly on pickpocket (ppk) expressing neurons, since reducing expression of this receptor in these neurons restores the ability to anticipate the LD transition in mated females. Furthermore, we provide evidence of connectivity between ppk+ neurons and the pigment-dispersing factor (PDF)-positive ventral lateral neurons (sLNv), which play a central role in the temporal organization of daily activity. Since PDF has been associated to the generation of the morning activity peak, we hypothesized that the mating signal could modulate PDF levels. Indeed, we confirm that mated females have reduced PDF levels at the dorsal protocerebrum; moreover, SPR downregulation in ppk+ neurons mimics PDF levels observed in males. In sum, our results are consistent with a model whereby mating-triggered signals reach clock neurons in the fly central nervous system to modulate the temporal organization of circadian behavior according to the needs of the new status. Public Library of Science 2022-12-22 /pmc/articles/PMC9779042/ /pubmed/36548223 http://dx.doi.org/10.1371/journal.pgen.1010258 Text en © 2022 Riva et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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
Riva, Sabrina
Ispizua, Juan Ignacio
Breide, María Trinidad
Polcowñuk, Sofía
Lobera, José Ricardo
Ceriani, María Fernanda
Risau-Gusman, Sebastian
Franco, Diana Lorena
Mating disrupts morning anticipation in Drosophila melanogaster females
title Mating disrupts morning anticipation in Drosophila melanogaster females
title_full Mating disrupts morning anticipation in Drosophila melanogaster females
title_fullStr Mating disrupts morning anticipation in Drosophila melanogaster females
title_full_unstemmed Mating disrupts morning anticipation in Drosophila melanogaster females
title_short Mating disrupts morning anticipation in Drosophila melanogaster females
title_sort mating disrupts morning anticipation in drosophila melanogaster females
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9779042/
https://www.ncbi.nlm.nih.gov/pubmed/36548223
http://dx.doi.org/10.1371/journal.pgen.1010258
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