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Using Pox-Neuro (Poxn) Mutants in Drosophila Gustation Research: A Double-Edged Sword

In Drosophila, Pox-neuro (Poxn) is a member of the Paired box (Pax) gene family that encodes transcription factors with characteristic paired DNA-binding domains. During embryonic development, Poxn is expressed in sensory organ precursor (SOP) cells of poly-innervated external sensory (p-es) organs...

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Autores principales: Chen, Yu-Chieh David, Park, Scarlet Jinhong, Ja, William W., Dahanukar, Anupama
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207628/
https://www.ncbi.nlm.nih.gov/pubmed/30405359
http://dx.doi.org/10.3389/fncel.2018.00382
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author Chen, Yu-Chieh David
Park, Scarlet Jinhong
Ja, William W.
Dahanukar, Anupama
author_facet Chen, Yu-Chieh David
Park, Scarlet Jinhong
Ja, William W.
Dahanukar, Anupama
author_sort Chen, Yu-Chieh David
collection PubMed
description In Drosophila, Pox-neuro (Poxn) is a member of the Paired box (Pax) gene family that encodes transcription factors with characteristic paired DNA-binding domains. During embryonic development, Poxn is expressed in sensory organ precursor (SOP) cells of poly-innervated external sensory (p-es) organs and is important for specifying p-es organ identity (chemosensory) as opposed to mono-innervated external sensory (m-es) organs (mechanosensory). In Poxn mutants, there is a transformation of chemosensory bristles into mechanosensory bristles. As a result, these mutants have often been considered to be entirely taste-blind, and researchers have used them in this capacity to investigate physiological and behavioral functions that act in a taste-independent manner. However, recent studies show that only external taste bristles are transformed in Poxn mutants whereas all internal pharyngeal taste neurons remain intact, raising concerns about interpretations of experimental results using Poxn mutants as taste-blind flies. In this review, we summarize the value of Poxn mutants in advancing our knowledge of taste-enriched genes and feeding behaviors, and encourage revisiting some of the conclusions about taste-independent nutrient-sensing mechanisms derived from these mutants. Lastly, we highlight that Poxn mutant flies remain a valuable tool for probing the function of the relatively understudied pharyngeal taste neurons in sensing meal properties and regulating feeding behaviors.
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spelling pubmed-62076282018-11-07 Using Pox-Neuro (Poxn) Mutants in Drosophila Gustation Research: A Double-Edged Sword Chen, Yu-Chieh David Park, Scarlet Jinhong Ja, William W. Dahanukar, Anupama Front Cell Neurosci Neuroscience In Drosophila, Pox-neuro (Poxn) is a member of the Paired box (Pax) gene family that encodes transcription factors with characteristic paired DNA-binding domains. During embryonic development, Poxn is expressed in sensory organ precursor (SOP) cells of poly-innervated external sensory (p-es) organs and is important for specifying p-es organ identity (chemosensory) as opposed to mono-innervated external sensory (m-es) organs (mechanosensory). In Poxn mutants, there is a transformation of chemosensory bristles into mechanosensory bristles. As a result, these mutants have often been considered to be entirely taste-blind, and researchers have used them in this capacity to investigate physiological and behavioral functions that act in a taste-independent manner. However, recent studies show that only external taste bristles are transformed in Poxn mutants whereas all internal pharyngeal taste neurons remain intact, raising concerns about interpretations of experimental results using Poxn mutants as taste-blind flies. In this review, we summarize the value of Poxn mutants in advancing our knowledge of taste-enriched genes and feeding behaviors, and encourage revisiting some of the conclusions about taste-independent nutrient-sensing mechanisms derived from these mutants. Lastly, we highlight that Poxn mutant flies remain a valuable tool for probing the function of the relatively understudied pharyngeal taste neurons in sensing meal properties and regulating feeding behaviors. Frontiers Media S.A. 2018-10-24 /pmc/articles/PMC6207628/ /pubmed/30405359 http://dx.doi.org/10.3389/fncel.2018.00382 Text en Copyright © 2018 Chen, Park, Ja and Dahanukar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Chen, Yu-Chieh David
Park, Scarlet Jinhong
Ja, William W.
Dahanukar, Anupama
Using Pox-Neuro (Poxn) Mutants in Drosophila Gustation Research: A Double-Edged Sword
title Using Pox-Neuro (Poxn) Mutants in Drosophila Gustation Research: A Double-Edged Sword
title_full Using Pox-Neuro (Poxn) Mutants in Drosophila Gustation Research: A Double-Edged Sword
title_fullStr Using Pox-Neuro (Poxn) Mutants in Drosophila Gustation Research: A Double-Edged Sword
title_full_unstemmed Using Pox-Neuro (Poxn) Mutants in Drosophila Gustation Research: A Double-Edged Sword
title_short Using Pox-Neuro (Poxn) Mutants in Drosophila Gustation Research: A Double-Edged Sword
title_sort using pox-neuro (poxn) mutants in drosophila gustation research: a double-edged sword
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207628/
https://www.ncbi.nlm.nih.gov/pubmed/30405359
http://dx.doi.org/10.3389/fncel.2018.00382
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