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An Allele of Sequoia Dominantly Enhances a Trio Mutant Phenotype to Influence Drosophila Larval Behavior

The transition of Drosophila third instar larvae from feeding, photo-phobic foragers to non-feeding, photo-neutral wanderers is a classic behavioral switch that precedes pupariation. The neuronal network responsible for this behavior has recently begun to be defined. Previous genetic analyses have i...

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Autores principales: Dean, Kathryn E., Fields, April, Geer, Marcus J., King, Eric C., Lynch, Brian T., Manohar, Rohan R., McCall, Julianne R., Palozola, Katherine C., Zhang, Yan, Liebl, Eric C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869853/
https://www.ncbi.nlm.nih.gov/pubmed/24376789
http://dx.doi.org/10.1371/journal.pone.0084149
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author Dean, Kathryn E.
Fields, April
Geer, Marcus J.
King, Eric C.
Lynch, Brian T.
Manohar, Rohan R.
McCall, Julianne R.
Palozola, Katherine C.
Zhang, Yan
Liebl, Eric C.
author_facet Dean, Kathryn E.
Fields, April
Geer, Marcus J.
King, Eric C.
Lynch, Brian T.
Manohar, Rohan R.
McCall, Julianne R.
Palozola, Katherine C.
Zhang, Yan
Liebl, Eric C.
author_sort Dean, Kathryn E.
collection PubMed
description The transition of Drosophila third instar larvae from feeding, photo-phobic foragers to non-feeding, photo-neutral wanderers is a classic behavioral switch that precedes pupariation. The neuronal network responsible for this behavior has recently begun to be defined. Previous genetic analyses have identified signaling components for food and light sensory inputs and neuropeptide hormonal outputs as being critical for the forager to wanderer transition. Trio is a Rho-Guanine Nucleotide Exchange Factor integrated into a variety of signaling networks including those governing axon pathfinding in early development. Sequoia is a pan-neuronally expressed zinc-finger transcription factor that governs dendrite and axon outgrowth. Using pre-pupal lethality as an endpoint, we have screened for dominant second-site enhancers of a weakly lethal trio mutant background. In these screens, an allele of sequoia has been identified. While these mutants have no obvious disruption of embryonic central nervous system architecture and survive to third instar larvae similar to controls, they retain forager behavior and thus fail to pupariate at high frequency.
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spelling pubmed-38698532013-12-27 An Allele of Sequoia Dominantly Enhances a Trio Mutant Phenotype to Influence Drosophila Larval Behavior Dean, Kathryn E. Fields, April Geer, Marcus J. King, Eric C. Lynch, Brian T. Manohar, Rohan R. McCall, Julianne R. Palozola, Katherine C. Zhang, Yan Liebl, Eric C. PLoS One Research Article The transition of Drosophila third instar larvae from feeding, photo-phobic foragers to non-feeding, photo-neutral wanderers is a classic behavioral switch that precedes pupariation. The neuronal network responsible for this behavior has recently begun to be defined. Previous genetic analyses have identified signaling components for food and light sensory inputs and neuropeptide hormonal outputs as being critical for the forager to wanderer transition. Trio is a Rho-Guanine Nucleotide Exchange Factor integrated into a variety of signaling networks including those governing axon pathfinding in early development. Sequoia is a pan-neuronally expressed zinc-finger transcription factor that governs dendrite and axon outgrowth. Using pre-pupal lethality as an endpoint, we have screened for dominant second-site enhancers of a weakly lethal trio mutant background. In these screens, an allele of sequoia has been identified. While these mutants have no obvious disruption of embryonic central nervous system architecture and survive to third instar larvae similar to controls, they retain forager behavior and thus fail to pupariate at high frequency. Public Library of Science 2013-12-20 /pmc/articles/PMC3869853/ /pubmed/24376789 http://dx.doi.org/10.1371/journal.pone.0084149 Text en © 2013 Dean 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
Dean, Kathryn E.
Fields, April
Geer, Marcus J.
King, Eric C.
Lynch, Brian T.
Manohar, Rohan R.
McCall, Julianne R.
Palozola, Katherine C.
Zhang, Yan
Liebl, Eric C.
An Allele of Sequoia Dominantly Enhances a Trio Mutant Phenotype to Influence Drosophila Larval Behavior
title An Allele of Sequoia Dominantly Enhances a Trio Mutant Phenotype to Influence Drosophila Larval Behavior
title_full An Allele of Sequoia Dominantly Enhances a Trio Mutant Phenotype to Influence Drosophila Larval Behavior
title_fullStr An Allele of Sequoia Dominantly Enhances a Trio Mutant Phenotype to Influence Drosophila Larval Behavior
title_full_unstemmed An Allele of Sequoia Dominantly Enhances a Trio Mutant Phenotype to Influence Drosophila Larval Behavior
title_short An Allele of Sequoia Dominantly Enhances a Trio Mutant Phenotype to Influence Drosophila Larval Behavior
title_sort allele of sequoia dominantly enhances a trio mutant phenotype to influence drosophila larval behavior
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869853/
https://www.ncbi.nlm.nih.gov/pubmed/24376789
http://dx.doi.org/10.1371/journal.pone.0084149
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