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Proper connectivity of Drosophila motion detector neurons requires Atonal function in progenitor cells

BACKGROUND: Vertebrates and invertebrates obtain visual motion information by channeling moving visual cues perceived by the retina through specific motion sensitive synaptic relays in the brain. In Drosophila, the series of synaptic relays forming the optic lobe are known as the lamina, medulla, lo...

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Autores principales: Oliva, Carlos, Choi, Ching-Man, Nicolai, Laura J J, Mora, Natalia, De Geest, Natalie, Hassan, Bassem A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941608/
https://www.ncbi.nlm.nih.gov/pubmed/24571981
http://dx.doi.org/10.1186/1749-8104-9-4
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author Oliva, Carlos
Choi, Ching-Man
Nicolai, Laura J J
Mora, Natalia
De Geest, Natalie
Hassan, Bassem A
author_facet Oliva, Carlos
Choi, Ching-Man
Nicolai, Laura J J
Mora, Natalia
De Geest, Natalie
Hassan, Bassem A
author_sort Oliva, Carlos
collection PubMed
description BACKGROUND: Vertebrates and invertebrates obtain visual motion information by channeling moving visual cues perceived by the retina through specific motion sensitive synaptic relays in the brain. In Drosophila, the series of synaptic relays forming the optic lobe are known as the lamina, medulla, lobula and lobula plate neuropiles. The fly’s motion detection output neurons, called the T4 and T5 cells, reside in the lobula plate. Adult optic lobe neurons are derived from larval neural progenitors in two proliferating compartments known as the outer and inner proliferation centers (OPC and IPC). Important insight has been gained into molecular mechanisms involved in the development of the lamina and medulla from the OPC, though less is known about the development of the lobula and lobula plate. RESULTS: Here we show that the proneural gene Atonal is expressed in a subset of IPC progenitors that give rise to the higher order motion detection neurons, T4 and T5, of the lobula plate. We also show that Atonal does not act as a proneural gene in this context. Rather, it is required specifically in IPC neural progenitors to regulate neurite outgrowth in the neuronal progeny. CONCLUSIONS: Our findings reveal that a proneural gene is expressed in progenitors but is required for neurite development of their progeny neurons. This suggests that transcriptional programs initiated specifically in progenitors are necessary for subsequent neuronal morphogenesis.
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spelling pubmed-39416082014-03-05 Proper connectivity of Drosophila motion detector neurons requires Atonal function in progenitor cells Oliva, Carlos Choi, Ching-Man Nicolai, Laura J J Mora, Natalia De Geest, Natalie Hassan, Bassem A Neural Dev Research Article BACKGROUND: Vertebrates and invertebrates obtain visual motion information by channeling moving visual cues perceived by the retina through specific motion sensitive synaptic relays in the brain. In Drosophila, the series of synaptic relays forming the optic lobe are known as the lamina, medulla, lobula and lobula plate neuropiles. The fly’s motion detection output neurons, called the T4 and T5 cells, reside in the lobula plate. Adult optic lobe neurons are derived from larval neural progenitors in two proliferating compartments known as the outer and inner proliferation centers (OPC and IPC). Important insight has been gained into molecular mechanisms involved in the development of the lamina and medulla from the OPC, though less is known about the development of the lobula and lobula plate. RESULTS: Here we show that the proneural gene Atonal is expressed in a subset of IPC progenitors that give rise to the higher order motion detection neurons, T4 and T5, of the lobula plate. We also show that Atonal does not act as a proneural gene in this context. Rather, it is required specifically in IPC neural progenitors to regulate neurite outgrowth in the neuronal progeny. CONCLUSIONS: Our findings reveal that a proneural gene is expressed in progenitors but is required for neurite development of their progeny neurons. This suggests that transcriptional programs initiated specifically in progenitors are necessary for subsequent neuronal morphogenesis. BioMed Central 2014-02-26 /pmc/articles/PMC3941608/ /pubmed/24571981 http://dx.doi.org/10.1186/1749-8104-9-4 Text en Copyright © 2014 Oliva et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Oliva, Carlos
Choi, Ching-Man
Nicolai, Laura J J
Mora, Natalia
De Geest, Natalie
Hassan, Bassem A
Proper connectivity of Drosophila motion detector neurons requires Atonal function in progenitor cells
title Proper connectivity of Drosophila motion detector neurons requires Atonal function in progenitor cells
title_full Proper connectivity of Drosophila motion detector neurons requires Atonal function in progenitor cells
title_fullStr Proper connectivity of Drosophila motion detector neurons requires Atonal function in progenitor cells
title_full_unstemmed Proper connectivity of Drosophila motion detector neurons requires Atonal function in progenitor cells
title_short Proper connectivity of Drosophila motion detector neurons requires Atonal function in progenitor cells
title_sort proper connectivity of drosophila motion detector neurons requires atonal function in progenitor cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941608/
https://www.ncbi.nlm.nih.gov/pubmed/24571981
http://dx.doi.org/10.1186/1749-8104-9-4
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