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Ultrabithorax confers spatial identity in a context-specific manner in the Drosophila postembryonic ventral nervous system

BACKGROUND: In holometabolous insects such as Drosophila melanogaster, neuroblasts produce an initial population of diverse neurons during embryogenesis and a much larger set of adult-specific neurons during larval life. In the ventral CNS, many of these secondary neuronal lineages differ significan...

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Autores principales: Marin, Elizabeth C, Dry, Katie E, Alaimo, Danielle R, Rudd, Kirstin T, Cillo, Anthony R, Clenshaw, Michael E, Negre, Nicolas, White, Kevin P, Truman, James W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520783/
https://www.ncbi.nlm.nih.gov/pubmed/22967828
http://dx.doi.org/10.1186/1749-8104-7-31
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author Marin, Elizabeth C
Dry, Katie E
Alaimo, Danielle R
Rudd, Kirstin T
Cillo, Anthony R
Clenshaw, Michael E
Negre, Nicolas
White, Kevin P
Truman, James W
author_facet Marin, Elizabeth C
Dry, Katie E
Alaimo, Danielle R
Rudd, Kirstin T
Cillo, Anthony R
Clenshaw, Michael E
Negre, Nicolas
White, Kevin P
Truman, James W
author_sort Marin, Elizabeth C
collection PubMed
description BACKGROUND: In holometabolous insects such as Drosophila melanogaster, neuroblasts produce an initial population of diverse neurons during embryogenesis and a much larger set of adult-specific neurons during larval life. In the ventral CNS, many of these secondary neuronal lineages differ significantly from one body segment to another, suggesting a role for anteroposterior patterning genes. RESULTS: Here we systematically characterize the expression pattern and function of the Hox gene Ultrabithorax (Ubx) in all 25 postembryonic lineages. We find that Ubx is expressed in a segment-, lineage-, and hemilineage-specific manner in the thoracic and anterior abdominal segments. When Ubx is removed from neuroblasts via mitotic recombination, neurons in these segments exhibit the morphologies and survival patterns of their anterior thoracic counterparts. Conversely, when Ubx is ectopically expressed in anterior thoracic segments, neurons exhibit complementary posterior transformation phenotypes. CONCLUSION: Our findings demonstrate that Ubx plays a critical role in conferring segment-appropriate morphology and survival on individual neurons in the adult-specific ventral CNS. Moreover, while always conferring spatial identity in some sense, Ubx has been co-opted during evolution for distinct and even opposite functions in different neuronal hemilineages.
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spelling pubmed-35207832012-12-13 Ultrabithorax confers spatial identity in a context-specific manner in the Drosophila postembryonic ventral nervous system Marin, Elizabeth C Dry, Katie E Alaimo, Danielle R Rudd, Kirstin T Cillo, Anthony R Clenshaw, Michael E Negre, Nicolas White, Kevin P Truman, James W Neural Dev Research Article BACKGROUND: In holometabolous insects such as Drosophila melanogaster, neuroblasts produce an initial population of diverse neurons during embryogenesis and a much larger set of adult-specific neurons during larval life. In the ventral CNS, many of these secondary neuronal lineages differ significantly from one body segment to another, suggesting a role for anteroposterior patterning genes. RESULTS: Here we systematically characterize the expression pattern and function of the Hox gene Ultrabithorax (Ubx) in all 25 postembryonic lineages. We find that Ubx is expressed in a segment-, lineage-, and hemilineage-specific manner in the thoracic and anterior abdominal segments. When Ubx is removed from neuroblasts via mitotic recombination, neurons in these segments exhibit the morphologies and survival patterns of their anterior thoracic counterparts. Conversely, when Ubx is ectopically expressed in anterior thoracic segments, neurons exhibit complementary posterior transformation phenotypes. CONCLUSION: Our findings demonstrate that Ubx plays a critical role in conferring segment-appropriate morphology and survival on individual neurons in the adult-specific ventral CNS. Moreover, while always conferring spatial identity in some sense, Ubx has been co-opted during evolution for distinct and even opposite functions in different neuronal hemilineages. BioMed Central 2012-09-11 /pmc/articles/PMC3520783/ /pubmed/22967828 http://dx.doi.org/10.1186/1749-8104-7-31 Text en Copyright ©2012 Marin 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 cited.
spellingShingle Research Article
Marin, Elizabeth C
Dry, Katie E
Alaimo, Danielle R
Rudd, Kirstin T
Cillo, Anthony R
Clenshaw, Michael E
Negre, Nicolas
White, Kevin P
Truman, James W
Ultrabithorax confers spatial identity in a context-specific manner in the Drosophila postembryonic ventral nervous system
title Ultrabithorax confers spatial identity in a context-specific manner in the Drosophila postembryonic ventral nervous system
title_full Ultrabithorax confers spatial identity in a context-specific manner in the Drosophila postembryonic ventral nervous system
title_fullStr Ultrabithorax confers spatial identity in a context-specific manner in the Drosophila postembryonic ventral nervous system
title_full_unstemmed Ultrabithorax confers spatial identity in a context-specific manner in the Drosophila postembryonic ventral nervous system
title_short Ultrabithorax confers spatial identity in a context-specific manner in the Drosophila postembryonic ventral nervous system
title_sort ultrabithorax confers spatial identity in a context-specific manner in the drosophila postembryonic ventral nervous system
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520783/
https://www.ncbi.nlm.nih.gov/pubmed/22967828
http://dx.doi.org/10.1186/1749-8104-7-31
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