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Neuroanatomical details of the lateral neurons of Drosophila melanogaster support their functional role in the circadian system

Drosophila melanogaster is a long‐standing model organism in the circadian clock research. A major advantage is the relative small number of about 150 neurons, which built the circadian clock in Drosophila. In our recent work, we focused on the neuroanatomical properties of the lateral neurons of th...

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Autores principales: Schubert, Frank K., Hagedorn, Nicolas, Yoshii, Taishi, Helfrich‐Förster, Charlotte, Rieger, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873451/
https://www.ncbi.nlm.nih.gov/pubmed/29424420
http://dx.doi.org/10.1002/cne.24406
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author Schubert, Frank K.
Hagedorn, Nicolas
Yoshii, Taishi
Helfrich‐Förster, Charlotte
Rieger, Dirk
author_facet Schubert, Frank K.
Hagedorn, Nicolas
Yoshii, Taishi
Helfrich‐Förster, Charlotte
Rieger, Dirk
author_sort Schubert, Frank K.
collection PubMed
description Drosophila melanogaster is a long‐standing model organism in the circadian clock research. A major advantage is the relative small number of about 150 neurons, which built the circadian clock in Drosophila. In our recent work, we focused on the neuroanatomical properties of the lateral neurons of the clock network. By applying the multicolor‐labeling technique Flybow we were able to identify the anatomical similarity of the previously described E2 subunit of the evening oscillator of the clock, which is built by the 5th small ventrolateral neuron (5th s‐LN(v)) and one ITP positive dorsolateral neuron (LN(d)). These two clock neurons share the same spatial and functional properties. We found both neurons innervating the same brain areas with similar pre‐ and postsynaptic sites in the brain. Here the anatomical findings support their shared function as a main evening oscillator in the clock network like also found in previous studies. A second quite surprising finding addresses the large lateral ventral PDF‐neurons (l‐LN(v)s). We could show that the four hardly distinguishable l‐LN(v)s consist of two subgroups with different innervation patterns. While three of the neurons reflect the well‐known branching pattern reproduced by PDF immunohistochemistry, one neuron per brain hemisphere has a distinguished innervation profile and is restricted only to the proximal part of the medulla‐surface. We named this neuron “extra” l‐LN(v) (l‐LN(v)x). We suggest the anatomical findings reflect different functional properties of the two l‐LN(v) subgroups.
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spelling pubmed-58734512018-03-31 Neuroanatomical details of the lateral neurons of Drosophila melanogaster support their functional role in the circadian system Schubert, Frank K. Hagedorn, Nicolas Yoshii, Taishi Helfrich‐Förster, Charlotte Rieger, Dirk J Comp Neurol Research Articles Drosophila melanogaster is a long‐standing model organism in the circadian clock research. A major advantage is the relative small number of about 150 neurons, which built the circadian clock in Drosophila. In our recent work, we focused on the neuroanatomical properties of the lateral neurons of the clock network. By applying the multicolor‐labeling technique Flybow we were able to identify the anatomical similarity of the previously described E2 subunit of the evening oscillator of the clock, which is built by the 5th small ventrolateral neuron (5th s‐LN(v)) and one ITP positive dorsolateral neuron (LN(d)). These two clock neurons share the same spatial and functional properties. We found both neurons innervating the same brain areas with similar pre‐ and postsynaptic sites in the brain. Here the anatomical findings support their shared function as a main evening oscillator in the clock network like also found in previous studies. A second quite surprising finding addresses the large lateral ventral PDF‐neurons (l‐LN(v)s). We could show that the four hardly distinguishable l‐LN(v)s consist of two subgroups with different innervation patterns. While three of the neurons reflect the well‐known branching pattern reproduced by PDF immunohistochemistry, one neuron per brain hemisphere has a distinguished innervation profile and is restricted only to the proximal part of the medulla‐surface. We named this neuron “extra” l‐LN(v) (l‐LN(v)x). We suggest the anatomical findings reflect different functional properties of the two l‐LN(v) subgroups. John Wiley and Sons Inc. 2018-02-26 2018-05-01 /pmc/articles/PMC5873451/ /pubmed/29424420 http://dx.doi.org/10.1002/cne.24406 Text en © 2018 The Authors The Journal of Comparative Neurology Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Schubert, Frank K.
Hagedorn, Nicolas
Yoshii, Taishi
Helfrich‐Förster, Charlotte
Rieger, Dirk
Neuroanatomical details of the lateral neurons of Drosophila melanogaster support their functional role in the circadian system
title Neuroanatomical details of the lateral neurons of Drosophila melanogaster support their functional role in the circadian system
title_full Neuroanatomical details of the lateral neurons of Drosophila melanogaster support their functional role in the circadian system
title_fullStr Neuroanatomical details of the lateral neurons of Drosophila melanogaster support their functional role in the circadian system
title_full_unstemmed Neuroanatomical details of the lateral neurons of Drosophila melanogaster support their functional role in the circadian system
title_short Neuroanatomical details of the lateral neurons of Drosophila melanogaster support their functional role in the circadian system
title_sort neuroanatomical details of the lateral neurons of drosophila melanogaster support their functional role in the circadian system
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873451/
https://www.ncbi.nlm.nih.gov/pubmed/29424420
http://dx.doi.org/10.1002/cne.24406
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