Developmentally Arrested Precursors of Pontine Neurons Establish an Embryonic Blueprint of the Drosophila Central Complex.


Journal

Current biology : CB
ISSN: 1879-0445
Titre abrégé: Curr Biol
Pays: England
ID NLM: 9107782

Informations de publication

Date de publication:
04 02 2019
Historique:
received: 14 08 2018
revised: 17 10 2018
accepted: 07 12 2018
pubmed: 22 1 2019
medline: 26 2 2020
entrez: 22 1 2019
Statut: ppublish

Résumé

Serial electron microscopic analysis shows that the Drosophila brain at hatching possesses a large fraction of developmentally arrested neurons with a small soma, heterochromatin-rich nucleus, and unbranched axon lacking synapses. We digitally reconstructed all 802 "small undifferentiated" (SU) neurons and assigned them to the known brain lineages. By establishing the coordinates and reconstructing trajectories of the SU neuron tracts, we provide a framework of landmarks for the ongoing analyses of the L1 brain circuitry. To address the later fate of SU neurons, we focused on the 54 SU neurons belonging to the DM1-DM4 lineages, which generate all columnar neurons of the central complex. Regarding their topologically ordered projection pattern, these neurons form an embryonic nucleus of the fan-shaped body ("FB pioneers"). Fan-shaped body pioneers survive into the adult stage, where they develop into a specific class of bi-columnar elements, the pontine neurons. Later born, unicolumnar DM1-DM4 neurons fasciculate with the fan-shaped body pioneers. Selective ablation of the fan-shaped body pioneers altered the architecture of the larval fan-shaped body primordium but did not result in gross abnormalities of the trajectories of unicolumnar neurons, indicating that axonal pathfinding of the two systems may be controlled independently. Our comprehensive spatial and developmental analysis of the SU neurons adds to our understanding of the establishment of neuronal circuitry.

Identifiants

pubmed: 30661802
pii: S0960-9822(18)31613-0
doi: 10.1016/j.cub.2018.12.012
pmc: PMC6524766
mid: NIHMS1519620
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

412-425.e3

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS054814
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS096290
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM007185
Pays : United States
Organisme : Howard Hughes Medical Institute
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

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Auteurs

Ingrid V Andrade (IV)

Department of Molecular Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA.

Nadia Riebli (N)

Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.

Bao-Chau M Nguyen (BM)

Department of Molecular Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA.

Jaison J Omoto (JJ)

Department of Molecular Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA.

Albert Cardona (A)

Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.

Volker Hartenstein (V)

Department of Molecular Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA. Electronic address: volkerh@mcdb.ucla.edu.

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