Cargando…
The neural basis for a persistent internal state in Drosophila females
Sustained changes in mood or action require persistent changes in neural activity, but it has been difficult to identify the neural circuit mechanisms that underlie persistent activity and contribute to long-lasting changes in behavior. Here, we show that a subset of Doublesex+ pC1 neurons in the Dr...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7787663/ https://www.ncbi.nlm.nih.gov/pubmed/33225998 http://dx.doi.org/10.7554/eLife.59502 |
_version_ | 1783632869685460992 |
---|---|
author | Deutsch, David Pacheco, Diego Encarnacion-Rivera, Lucas Pereira, Talmo Fathy, Ramie Clemens, Jan Girardin, Cyrille Calhoun, Adam Ireland, Elise Burke, Austin Dorkenwald, Sven McKellar, Claire Macrina, Thomas Lu, Ran Lee, Kisuk Kemnitz, Nico Ih, Dodam Castro, Manuel Halageri, Akhilesh Jordan, Chris Silversmith, William Wu, Jingpeng Seung, H Sebastian Murthy, Mala |
author_facet | Deutsch, David Pacheco, Diego Encarnacion-Rivera, Lucas Pereira, Talmo Fathy, Ramie Clemens, Jan Girardin, Cyrille Calhoun, Adam Ireland, Elise Burke, Austin Dorkenwald, Sven McKellar, Claire Macrina, Thomas Lu, Ran Lee, Kisuk Kemnitz, Nico Ih, Dodam Castro, Manuel Halageri, Akhilesh Jordan, Chris Silversmith, William Wu, Jingpeng Seung, H Sebastian Murthy, Mala |
author_sort | Deutsch, David |
collection | PubMed |
description | Sustained changes in mood or action require persistent changes in neural activity, but it has been difficult to identify the neural circuit mechanisms that underlie persistent activity and contribute to long-lasting changes in behavior. Here, we show that a subset of Doublesex+ pC1 neurons in the Drosophila female brain, called pC1d/e, can drive minutes-long changes in female behavior in the presence of males. Using automated reconstruction of a volume electron microscopic (EM) image of the female brain, we map all inputs and outputs to both pC1d and pC1e. This reveals strong recurrent connectivity between, in particular, pC1d/e neurons and a specific subset of Fruitless+ neurons called aIPg. We additionally find that pC1d/e activation drives long-lasting persistent neural activity in brain areas and cells overlapping with the pC1d/e neural network, including both Doublesex+ and Fruitless+ neurons. Our work thus links minutes-long persistent changes in behavior with persistent neural activity and recurrent circuit architecture in the female brain. |
format | Online Article Text |
id | pubmed-7787663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-77876632021-01-11 The neural basis for a persistent internal state in Drosophila females Deutsch, David Pacheco, Diego Encarnacion-Rivera, Lucas Pereira, Talmo Fathy, Ramie Clemens, Jan Girardin, Cyrille Calhoun, Adam Ireland, Elise Burke, Austin Dorkenwald, Sven McKellar, Claire Macrina, Thomas Lu, Ran Lee, Kisuk Kemnitz, Nico Ih, Dodam Castro, Manuel Halageri, Akhilesh Jordan, Chris Silversmith, William Wu, Jingpeng Seung, H Sebastian Murthy, Mala eLife Neuroscience Sustained changes in mood or action require persistent changes in neural activity, but it has been difficult to identify the neural circuit mechanisms that underlie persistent activity and contribute to long-lasting changes in behavior. Here, we show that a subset of Doublesex+ pC1 neurons in the Drosophila female brain, called pC1d/e, can drive minutes-long changes in female behavior in the presence of males. Using automated reconstruction of a volume electron microscopic (EM) image of the female brain, we map all inputs and outputs to both pC1d and pC1e. This reveals strong recurrent connectivity between, in particular, pC1d/e neurons and a specific subset of Fruitless+ neurons called aIPg. We additionally find that pC1d/e activation drives long-lasting persistent neural activity in brain areas and cells overlapping with the pC1d/e neural network, including both Doublesex+ and Fruitless+ neurons. Our work thus links minutes-long persistent changes in behavior with persistent neural activity and recurrent circuit architecture in the female brain. eLife Sciences Publications, Ltd 2020-11-23 /pmc/articles/PMC7787663/ /pubmed/33225998 http://dx.doi.org/10.7554/eLife.59502 Text en © 2020, Deutsch et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Deutsch, David Pacheco, Diego Encarnacion-Rivera, Lucas Pereira, Talmo Fathy, Ramie Clemens, Jan Girardin, Cyrille Calhoun, Adam Ireland, Elise Burke, Austin Dorkenwald, Sven McKellar, Claire Macrina, Thomas Lu, Ran Lee, Kisuk Kemnitz, Nico Ih, Dodam Castro, Manuel Halageri, Akhilesh Jordan, Chris Silversmith, William Wu, Jingpeng Seung, H Sebastian Murthy, Mala The neural basis for a persistent internal state in Drosophila females |
title | The neural basis for a persistent internal state in Drosophila females |
title_full | The neural basis for a persistent internal state in Drosophila females |
title_fullStr | The neural basis for a persistent internal state in Drosophila females |
title_full_unstemmed | The neural basis for a persistent internal state in Drosophila females |
title_short | The neural basis for a persistent internal state in Drosophila females |
title_sort | neural basis for a persistent internal state in drosophila females |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7787663/ https://www.ncbi.nlm.nih.gov/pubmed/33225998 http://dx.doi.org/10.7554/eLife.59502 |
work_keys_str_mv | AT deutschdavid theneuralbasisforapersistentinternalstateindrosophilafemales AT pachecodiego theneuralbasisforapersistentinternalstateindrosophilafemales AT encarnacionriveralucas theneuralbasisforapersistentinternalstateindrosophilafemales AT pereiratalmo theneuralbasisforapersistentinternalstateindrosophilafemales AT fathyramie theneuralbasisforapersistentinternalstateindrosophilafemales AT clemensjan theneuralbasisforapersistentinternalstateindrosophilafemales AT girardincyrille theneuralbasisforapersistentinternalstateindrosophilafemales AT calhounadam theneuralbasisforapersistentinternalstateindrosophilafemales AT irelandelise theneuralbasisforapersistentinternalstateindrosophilafemales AT burkeaustin theneuralbasisforapersistentinternalstateindrosophilafemales AT dorkenwaldsven theneuralbasisforapersistentinternalstateindrosophilafemales AT mckellarclaire theneuralbasisforapersistentinternalstateindrosophilafemales AT macrinathomas theneuralbasisforapersistentinternalstateindrosophilafemales AT luran theneuralbasisforapersistentinternalstateindrosophilafemales AT leekisuk theneuralbasisforapersistentinternalstateindrosophilafemales AT kemnitznico theneuralbasisforapersistentinternalstateindrosophilafemales AT ihdodam theneuralbasisforapersistentinternalstateindrosophilafemales AT castromanuel theneuralbasisforapersistentinternalstateindrosophilafemales AT halageriakhilesh theneuralbasisforapersistentinternalstateindrosophilafemales AT jordanchris theneuralbasisforapersistentinternalstateindrosophilafemales AT silversmithwilliam theneuralbasisforapersistentinternalstateindrosophilafemales AT wujingpeng theneuralbasisforapersistentinternalstateindrosophilafemales AT seunghsebastian theneuralbasisforapersistentinternalstateindrosophilafemales AT murthymala theneuralbasisforapersistentinternalstateindrosophilafemales AT deutschdavid neuralbasisforapersistentinternalstateindrosophilafemales AT pachecodiego neuralbasisforapersistentinternalstateindrosophilafemales AT encarnacionriveralucas neuralbasisforapersistentinternalstateindrosophilafemales AT pereiratalmo neuralbasisforapersistentinternalstateindrosophilafemales AT fathyramie neuralbasisforapersistentinternalstateindrosophilafemales AT clemensjan neuralbasisforapersistentinternalstateindrosophilafemales AT girardincyrille neuralbasisforapersistentinternalstateindrosophilafemales AT calhounadam neuralbasisforapersistentinternalstateindrosophilafemales AT irelandelise neuralbasisforapersistentinternalstateindrosophilafemales AT burkeaustin neuralbasisforapersistentinternalstateindrosophilafemales AT dorkenwaldsven neuralbasisforapersistentinternalstateindrosophilafemales AT mckellarclaire neuralbasisforapersistentinternalstateindrosophilafemales AT macrinathomas neuralbasisforapersistentinternalstateindrosophilafemales AT luran neuralbasisforapersistentinternalstateindrosophilafemales AT leekisuk neuralbasisforapersistentinternalstateindrosophilafemales AT kemnitznico neuralbasisforapersistentinternalstateindrosophilafemales AT ihdodam neuralbasisforapersistentinternalstateindrosophilafemales AT castromanuel neuralbasisforapersistentinternalstateindrosophilafemales AT halageriakhilesh neuralbasisforapersistentinternalstateindrosophilafemales AT jordanchris neuralbasisforapersistentinternalstateindrosophilafemales AT silversmithwilliam neuralbasisforapersistentinternalstateindrosophilafemales AT wujingpeng neuralbasisforapersistentinternalstateindrosophilafemales AT seunghsebastian neuralbasisforapersistentinternalstateindrosophilafemales AT murthymala neuralbasisforapersistentinternalstateindrosophilafemales |