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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/38027
Ver los metadatos del registro completo
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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 |
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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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score |
12.982451 |