Cargando…

Rhomboid Enhancer Activity Defines a Subset of Drosophila Neural Precursors Required for Proper Feeding, Growth and Viability

Organismal growth regulation requires the interaction of multiple metabolic, hormonal and neuronal pathways. While the molecular basis for many of these are well characterized, less is known about the developmental origins of growth regulatory structures and the mechanisms governing control of feedi...

Descripción completa

Detalles Bibliográficos
Autores principales: Gresser, Amy L., Gutzwiller, Lisa M., Gauck, Mackenzie K., Hartenstein, Volker, Cook, Tiffany A., Gebelein, Brian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529294/
https://www.ncbi.nlm.nih.gov/pubmed/26252385
http://dx.doi.org/10.1371/journal.pone.0134915
_version_ 1782384778660544512
author Gresser, Amy L.
Gutzwiller, Lisa M.
Gauck, Mackenzie K.
Hartenstein, Volker
Cook, Tiffany A.
Gebelein, Brian
author_facet Gresser, Amy L.
Gutzwiller, Lisa M.
Gauck, Mackenzie K.
Hartenstein, Volker
Cook, Tiffany A.
Gebelein, Brian
author_sort Gresser, Amy L.
collection PubMed
description Organismal growth regulation requires the interaction of multiple metabolic, hormonal and neuronal pathways. While the molecular basis for many of these are well characterized, less is known about the developmental origins of growth regulatory structures and the mechanisms governing control of feeding and satiety. For these reasons, new tools and approaches are needed to link the specification and maturation of discrete cell populations with their subsequent regulatory roles. In this study, we characterize a rhomboid enhancer element that selectively labels four Drosophila embryonic neural precursors. These precursors give rise to the hypopharyngeal sensory organ of the peripheral nervous system and a subset of neurons in the deutocerebral region of the embryonic central nervous system. Post embryogenesis, the rhomboid enhancer is active in a subset of cells within the larval pharyngeal epithelium. Enhancer-targeted toxin expression alters the morphology of the sense organ and results in impaired larval growth, developmental delay, defective anterior spiracle eversion and lethality. Limiting the duration of toxin expression reveals differences in the critical periods for these effects. Embryonic expression causes developmental defects and partially penetrant pre-pupal lethality. Survivors of embryonic expression, however, ultimately become viable adults. In contrast, post-embryonic toxin expression results in fully penetrant lethality. To better define the larval growth defect, we used a variety of assays to demonstrate that toxin-targeted larvae are capable of locating, ingesting and clearing food and they exhibit normal food search behaviors. Strikingly, however, following food exposure these larvae show a rapid decrease in consumption suggesting a satiety-like phenomenon that correlates with the period of impaired larval growth. Together, these data suggest a critical role for these enhancer-defined lineages in regulating feeding, growth and viability.
format Online
Article
Text
id pubmed-4529294
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-45292942015-08-12 Rhomboid Enhancer Activity Defines a Subset of Drosophila Neural Precursors Required for Proper Feeding, Growth and Viability Gresser, Amy L. Gutzwiller, Lisa M. Gauck, Mackenzie K. Hartenstein, Volker Cook, Tiffany A. Gebelein, Brian PLoS One Research Article Organismal growth regulation requires the interaction of multiple metabolic, hormonal and neuronal pathways. While the molecular basis for many of these are well characterized, less is known about the developmental origins of growth regulatory structures and the mechanisms governing control of feeding and satiety. For these reasons, new tools and approaches are needed to link the specification and maturation of discrete cell populations with their subsequent regulatory roles. In this study, we characterize a rhomboid enhancer element that selectively labels four Drosophila embryonic neural precursors. These precursors give rise to the hypopharyngeal sensory organ of the peripheral nervous system and a subset of neurons in the deutocerebral region of the embryonic central nervous system. Post embryogenesis, the rhomboid enhancer is active in a subset of cells within the larval pharyngeal epithelium. Enhancer-targeted toxin expression alters the morphology of the sense organ and results in impaired larval growth, developmental delay, defective anterior spiracle eversion and lethality. Limiting the duration of toxin expression reveals differences in the critical periods for these effects. Embryonic expression causes developmental defects and partially penetrant pre-pupal lethality. Survivors of embryonic expression, however, ultimately become viable adults. In contrast, post-embryonic toxin expression results in fully penetrant lethality. To better define the larval growth defect, we used a variety of assays to demonstrate that toxin-targeted larvae are capable of locating, ingesting and clearing food and they exhibit normal food search behaviors. Strikingly, however, following food exposure these larvae show a rapid decrease in consumption suggesting a satiety-like phenomenon that correlates with the period of impaired larval growth. Together, these data suggest a critical role for these enhancer-defined lineages in regulating feeding, growth and viability. Public Library of Science 2015-08-07 /pmc/articles/PMC4529294/ /pubmed/26252385 http://dx.doi.org/10.1371/journal.pone.0134915 Text en © 2015 Gresser et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gresser, Amy L.
Gutzwiller, Lisa M.
Gauck, Mackenzie K.
Hartenstein, Volker
Cook, Tiffany A.
Gebelein, Brian
Rhomboid Enhancer Activity Defines a Subset of Drosophila Neural Precursors Required for Proper Feeding, Growth and Viability
title Rhomboid Enhancer Activity Defines a Subset of Drosophila Neural Precursors Required for Proper Feeding, Growth and Viability
title_full Rhomboid Enhancer Activity Defines a Subset of Drosophila Neural Precursors Required for Proper Feeding, Growth and Viability
title_fullStr Rhomboid Enhancer Activity Defines a Subset of Drosophila Neural Precursors Required for Proper Feeding, Growth and Viability
title_full_unstemmed Rhomboid Enhancer Activity Defines a Subset of Drosophila Neural Precursors Required for Proper Feeding, Growth and Viability
title_short Rhomboid Enhancer Activity Defines a Subset of Drosophila Neural Precursors Required for Proper Feeding, Growth and Viability
title_sort rhomboid enhancer activity defines a subset of drosophila neural precursors required for proper feeding, growth and viability
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529294/
https://www.ncbi.nlm.nih.gov/pubmed/26252385
http://dx.doi.org/10.1371/journal.pone.0134915
work_keys_str_mv AT gresseramyl rhomboidenhanceractivitydefinesasubsetofdrosophilaneuralprecursorsrequiredforproperfeedinggrowthandviability
AT gutzwillerlisam rhomboidenhanceractivitydefinesasubsetofdrosophilaneuralprecursorsrequiredforproperfeedinggrowthandviability
AT gauckmackenziek rhomboidenhanceractivitydefinesasubsetofdrosophilaneuralprecursorsrequiredforproperfeedinggrowthandviability
AT hartensteinvolker rhomboidenhanceractivitydefinesasubsetofdrosophilaneuralprecursorsrequiredforproperfeedinggrowthandviability
AT cooktiffanya rhomboidenhanceractivitydefinesasubsetofdrosophilaneuralprecursorsrequiredforproperfeedinggrowthandviability
AT gebeleinbrian rhomboidenhanceractivitydefinesasubsetofdrosophilaneuralprecursorsrequiredforproperfeedinggrowthandviability