Impaired clock output by altered connectivity in the circadian network

Autores
Fernandez, Maria de la Paz; Chu, Jessie; Villella, Adriana; Atkinson, Nigel; Kay, Steve A.; Ceriani, Maria Fernanda
Año de publicación
2007
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Substantial progress has been made in elucidating the molecular processes that impart a temporal control to physiology and behavior in most eukaryotes. In Drosophila, dorsal and ventral neuronal networks act in concert to convey rhythmicity. Recently, the hierarchical organization among the different circadian clusters has been addressed, but how molecular oscillations translate into rhythmic behavior remains unclear. The small ventral lateral neurons can synchronize certain dorsal oscillators likely through the release of pigment dispersing factor (PDF), a neuropeptide central to the control of rhythmic rest-activity cycles. In the present study, we have taken advantage of flies exhibiting a distinctive arrhythmic phenotype due to mutation of the potassium channel slowpoke (slo) to examine the relevance of specific neuronal populations involved in the circadian control of behavior. We show that altered neuronal function associated with the null mutation specifically impaired PDF accumulation in the dorsal protocerebrum and, in turn, desynchronized molecular oscillations in the dorsal clusters. However, molecular oscillations in the small ventral lateral neurons are properly running in the null mutant, indicating that slo is acting downstream of these core pacemaker cells, most likely in the output pathway. Surprisingly, disrupted PDF signaling by slo dysfunction directly affects the structure of the underlying circuit. Our observations demonstrate that subtle structural changes within the circadian network are responsible for behavioral arrhythmicity.
Fil: Fernandez, Maria de la Paz. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
Fil: Chu, Jessie. The Scripps Research Institute; Estados Unidos
Fil: Villella, Adriana. Brandeis University; Estados Unidos
Fil: Atkinson, Nigel. University of Texas; Estados Unidos
Fil: Kay, Steve A.. The Scripps Research Institute; Estados Unidos
Fil: Ceriani, Maria Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
Materia
Circadian Circuitry
Drosophila
Pigment Dispersing Factor
Potassium Channels
Nivel de accesibilidad
acceso embargado
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/38027

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spelling Impaired clock output by altered connectivity in the circadian networkFernandez, Maria de la PazChu, JessieVillella, AdrianaAtkinson, NigelKay, Steve A.Ceriani, Maria FernandaCircadian CircuitryDrosophilaPigment Dispersing FactorPotassium Channelshttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Substantial progress has been made in elucidating the molecular processes that impart a temporal control to physiology and behavior in most eukaryotes. In Drosophila, dorsal and ventral neuronal networks act in concert to convey rhythmicity. Recently, the hierarchical organization among the different circadian clusters has been addressed, but how molecular oscillations translate into rhythmic behavior remains unclear. The small ventral lateral neurons can synchronize certain dorsal oscillators likely through the release of pigment dispersing factor (PDF), a neuropeptide central to the control of rhythmic rest-activity cycles. In the present study, we have taken advantage of flies exhibiting a distinctive arrhythmic phenotype due to mutation of the potassium channel slowpoke (slo) to examine the relevance of specific neuronal populations involved in the circadian control of behavior. We show that altered neuronal function associated with the null mutation specifically impaired PDF accumulation in the dorsal protocerebrum and, in turn, desynchronized molecular oscillations in the dorsal clusters. However, molecular oscillations in the small ventral lateral neurons are properly running in the null mutant, indicating that slo is acting downstream of these core pacemaker cells, most likely in the output pathway. Surprisingly, disrupted PDF signaling by slo dysfunction directly affects the structure of the underlying circuit. Our observations demonstrate that subtle structural changes within the circadian network are responsible for behavioral arrhythmicity.Fil: Fernandez, Maria de la Paz. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; ArgentinaFil: Chu, Jessie. The Scripps Research Institute; Estados UnidosFil: Villella, Adriana. Brandeis University; Estados UnidosFil: Atkinson, Nigel. University of Texas; Estados UnidosFil: Kay, Steve A.. The Scripps Research Institute; Estados UnidosFil: Ceriani, Maria Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; ArgentinaNational Academy of Sciences2007-03info:eu-repo/date/embargoEnd/2007-10-27info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/38027Fernandez, Maria de la Paz; Chu, Jessie; Villella, Adriana; Atkinson, Nigel; Kay, Steve A.; et al.; Impaired clock output by altered connectivity in the circadian network; National Academy of Sciences; Proceedings of the National Academy of Sciences of The United States of America; 104; 13; 3-2007; 5650-56550027-84241091-6490CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1073/pnas.0608260104info:eu-repo/semantics/altIdentifier/url/http://www.pnas.org/content/104/13/5650.longinfo:eu-repo/semantics/embargoedAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T11:44:00Zoai:ri.conicet.gov.ar:11336/38027instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 11:44:00.265CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Impaired clock output by altered connectivity in the circadian network
title Impaired clock output by altered connectivity in the circadian network
spellingShingle Impaired clock output by altered connectivity in the circadian network
Fernandez, Maria de la Paz
Circadian Circuitry
Drosophila
Pigment Dispersing Factor
Potassium Channels
title_short Impaired clock output by altered connectivity in the circadian network
title_full Impaired clock output by altered connectivity in the circadian network
title_fullStr Impaired clock output by altered connectivity in the circadian network
title_full_unstemmed Impaired clock output by altered connectivity in the circadian network
title_sort Impaired clock output by altered connectivity in the circadian network
dc.creator.none.fl_str_mv Fernandez, Maria de la Paz
Chu, Jessie
Villella, Adriana
Atkinson, Nigel
Kay, Steve A.
Ceriani, Maria Fernanda
author Fernandez, Maria de la Paz
author_facet Fernandez, Maria de la Paz
Chu, Jessie
Villella, Adriana
Atkinson, Nigel
Kay, Steve A.
Ceriani, Maria Fernanda
author_role author
author2 Chu, Jessie
Villella, Adriana
Atkinson, Nigel
Kay, Steve A.
Ceriani, Maria Fernanda
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Circadian Circuitry
Drosophila
Pigment Dispersing Factor
Potassium Channels
topic Circadian Circuitry
Drosophila
Pigment Dispersing Factor
Potassium Channels
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.1
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Substantial progress has been made in elucidating the molecular processes that impart a temporal control to physiology and behavior in most eukaryotes. In Drosophila, dorsal and ventral neuronal networks act in concert to convey rhythmicity. Recently, the hierarchical organization among the different circadian clusters has been addressed, but how molecular oscillations translate into rhythmic behavior remains unclear. The small ventral lateral neurons can synchronize certain dorsal oscillators likely through the release of pigment dispersing factor (PDF), a neuropeptide central to the control of rhythmic rest-activity cycles. In the present study, we have taken advantage of flies exhibiting a distinctive arrhythmic phenotype due to mutation of the potassium channel slowpoke (slo) to examine the relevance of specific neuronal populations involved in the circadian control of behavior. We show that altered neuronal function associated with the null mutation specifically impaired PDF accumulation in the dorsal protocerebrum and, in turn, desynchronized molecular oscillations in the dorsal clusters. However, molecular oscillations in the small ventral lateral neurons are properly running in the null mutant, indicating that slo is acting downstream of these core pacemaker cells, most likely in the output pathway. Surprisingly, disrupted PDF signaling by slo dysfunction directly affects the structure of the underlying circuit. Our observations demonstrate that subtle structural changes within the circadian network are responsible for behavioral arrhythmicity.
Fil: Fernandez, Maria de la Paz. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
Fil: Chu, Jessie. The Scripps Research Institute; Estados Unidos
Fil: Villella, Adriana. Brandeis University; Estados Unidos
Fil: Atkinson, Nigel. University of Texas; Estados Unidos
Fil: Kay, Steve A.. The Scripps Research Institute; Estados Unidos
Fil: Ceriani, Maria Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
description Substantial progress has been made in elucidating the molecular processes that impart a temporal control to physiology and behavior in most eukaryotes. In Drosophila, dorsal and ventral neuronal networks act in concert to convey rhythmicity. Recently, the hierarchical organization among the different circadian clusters has been addressed, but how molecular oscillations translate into rhythmic behavior remains unclear. The small ventral lateral neurons can synchronize certain dorsal oscillators likely through the release of pigment dispersing factor (PDF), a neuropeptide central to the control of rhythmic rest-activity cycles. In the present study, we have taken advantage of flies exhibiting a distinctive arrhythmic phenotype due to mutation of the potassium channel slowpoke (slo) to examine the relevance of specific neuronal populations involved in the circadian control of behavior. We show that altered neuronal function associated with the null mutation specifically impaired PDF accumulation in the dorsal protocerebrum and, in turn, desynchronized molecular oscillations in the dorsal clusters. However, molecular oscillations in the small ventral lateral neurons are properly running in the null mutant, indicating that slo is acting downstream of these core pacemaker cells, most likely in the output pathway. Surprisingly, disrupted PDF signaling by slo dysfunction directly affects the structure of the underlying circuit. Our observations demonstrate that subtle structural changes within the circadian network are responsible for behavioral arrhythmicity.
publishDate 2007
dc.date.none.fl_str_mv 2007-03
info:eu-repo/date/embargoEnd/2007-10-27
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/38027
Fernandez, Maria de la Paz; Chu, Jessie; Villella, Adriana; Atkinson, Nigel; Kay, Steve A.; et al.; Impaired clock output by altered connectivity in the circadian network; National Academy of Sciences; Proceedings of the National Academy of Sciences of The United States of America; 104; 13; 3-2007; 5650-5655
0027-8424
1091-6490
CONICET Digital
CONICET
url http://hdl.handle.net/11336/38027
identifier_str_mv Fernandez, Maria de la Paz; Chu, Jessie; Villella, Adriana; Atkinson, Nigel; Kay, Steve A.; et al.; Impaired clock output by altered connectivity in the circadian network; National Academy of Sciences; Proceedings of the National Academy of Sciences of The United States of America; 104; 13; 3-2007; 5650-5655
0027-8424
1091-6490
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1073/pnas.0608260104
info:eu-repo/semantics/altIdentifier/url/http://www.pnas.org/content/104/13/5650.long
dc.rights.none.fl_str_mv info:eu-repo/semantics/embargoedAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv embargoedAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv National Academy of Sciences
publisher.none.fl_str_mv National Academy of Sciences
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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