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The Logic of Circadian Organization in Drosophila
BACKGROUND: In the fruit fly Drosophila melanogaster, interlocked negative transcription/translation feedback loops provide the core of the circadian clock that generates rhythmic phenotypes. Although the current molecular model portrays the oscillator as cell autonomous, cross-talk among clock neur...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4188814/ https://www.ncbi.nlm.nih.gov/pubmed/25220056 http://dx.doi.org/10.1016/j.cub.2014.08.023 |
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author | Dissel, Stephane Hansen, Celia N. Özkaya, Özge Hemsley, Matthew Kyriacou, Charalambos P. Rosato, Ezio |
author_facet | Dissel, Stephane Hansen, Celia N. Özkaya, Özge Hemsley, Matthew Kyriacou, Charalambos P. Rosato, Ezio |
author_sort | Dissel, Stephane |
collection | PubMed |
description | BACKGROUND: In the fruit fly Drosophila melanogaster, interlocked negative transcription/translation feedback loops provide the core of the circadian clock that generates rhythmic phenotypes. Although the current molecular model portrays the oscillator as cell autonomous, cross-talk among clock neurons is essential for robust cycling behavior. Nevertheless, the functional organization of the neuronal network remains obscure. RESULTS: Here we show that shortening or lengthening of the circadian period of locomotor activity can be obtained either by targeting different groups of clock cells with the same genetic manipulation or by challenging the same group of cells with activators and repressors of neuronal excitability. CONCLUSIONS: Based on these observations we interpret circadian rhythmicity as an emerging property of the circadian network and we propose an initial model for its architectural design. |
format | Online Article Text |
id | pubmed-4188814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41888142014-10-13 The Logic of Circadian Organization in Drosophila Dissel, Stephane Hansen, Celia N. Özkaya, Özge Hemsley, Matthew Kyriacou, Charalambos P. Rosato, Ezio Curr Biol Article BACKGROUND: In the fruit fly Drosophila melanogaster, interlocked negative transcription/translation feedback loops provide the core of the circadian clock that generates rhythmic phenotypes. Although the current molecular model portrays the oscillator as cell autonomous, cross-talk among clock neurons is essential for robust cycling behavior. Nevertheless, the functional organization of the neuronal network remains obscure. RESULTS: Here we show that shortening or lengthening of the circadian period of locomotor activity can be obtained either by targeting different groups of clock cells with the same genetic manipulation or by challenging the same group of cells with activators and repressors of neuronal excitability. CONCLUSIONS: Based on these observations we interpret circadian rhythmicity as an emerging property of the circadian network and we propose an initial model for its architectural design. Cell Press 2014-10-06 /pmc/articles/PMC4188814/ /pubmed/25220056 http://dx.doi.org/10.1016/j.cub.2014.08.023 Text en © 2014 The Authors https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) . |
spellingShingle | Article Dissel, Stephane Hansen, Celia N. Özkaya, Özge Hemsley, Matthew Kyriacou, Charalambos P. Rosato, Ezio The Logic of Circadian Organization in Drosophila |
title | The Logic of Circadian Organization in Drosophila |
title_full | The Logic of Circadian Organization in Drosophila |
title_fullStr | The Logic of Circadian Organization in Drosophila |
title_full_unstemmed | The Logic of Circadian Organization in Drosophila |
title_short | The Logic of Circadian Organization in Drosophila |
title_sort | logic of circadian organization in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4188814/ https://www.ncbi.nlm.nih.gov/pubmed/25220056 http://dx.doi.org/10.1016/j.cub.2014.08.023 |
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