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PMID: 7576627 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Developmental defects in brain segmentation caused by mutations of the homeobox genes orthodenticle and empty spiracles in Drosophila.

Neuron ·Vol. 15 ·No. 4 ·1995-10-00 ·Pages 769-78

Hirth F, Therianos S, Loop T, Gehring WJ, Reichert H, Furukubo-Tokunaga K

Abstract

We have studied the roles of the homeobox genes orthodenticle (otd) and empty spiracles (ems) in embryonic brain development of Drosophila. The embryonic brain is composed of three segmental neuromeres. The otd gene is expressed predominantly in the anterior neuromere; expression of ems is restricted to the two posterior neuromeres. Mutation of otd eliminates the first (protocerebral) brain neuromere. Mutation of ems eliminates the second (deutocerebral) and third (tritocerebral) neuromeres. otd is also necessary for development of the dorsal protocerebrum of the adult brain. We conclude that these homeobox genes are required for the development of specific brain segments in Drosophila, and that the regionalized expression of their homologs in vertebrate brains suggests an evolutionarily conserved program for brain development.

MeSH Terms
Animals Brain/embryology,growth & development,metabolism Drosophila/embryology,genetics Drosophila Proteins Gene Expression Genes, Homeobox Homeodomain Proteins/genetics,physiology Immunoenzyme Techniques Mutation Neurons/metabolism
Chemicals
Drosophila Proteins Homeodomain Proteins ems protein, Drosophila oc protein, Drosophila
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Hirth F
Laboratory of Neurobiology, University of Basel, Switzerland.
Therianos S
Loop T
Gehring W J
Reichert H
Furukubo-Tokunaga K
Article Info
Journal
Neuron
Abbr.
Neuron
ISSN
0896-6273
Published
1995-10-00
Pages
769-78
Language
English
Region
United States
NLM ID
8809320
Subset
IM
Grants
NICHD NIH HHS · N01-HD-2-3144 · United States
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