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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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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. |
format | Online Article Text |
id | pubmed-3869853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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