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Transcriptional profiling of olfactory system development identifies distal antenna as a regulator of subset of neuronal fates
Drosophila uses 50 different olfactory receptor neuron (ORN) classes that are clustered within distinct sensilla subtypes to decipher their chemical environment. Each sensilla subtype houses 1–4 ORN identities that arise through asymmetric divisions of a single sensory organ precursor (SOP). Despite...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244397/ https://www.ncbi.nlm.nih.gov/pubmed/28102318 http://dx.doi.org/10.1038/srep40873 |
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author | Barish, Scott Li, Qingyun Pan, Jia W. Soeder, Charlie Jones, Corbin Volkan, Pelin C. |
author_facet | Barish, Scott Li, Qingyun Pan, Jia W. Soeder, Charlie Jones, Corbin Volkan, Pelin C. |
author_sort | Barish, Scott |
collection | PubMed |
description | Drosophila uses 50 different olfactory receptor neuron (ORN) classes that are clustered within distinct sensilla subtypes to decipher their chemical environment. Each sensilla subtype houses 1–4 ORN identities that arise through asymmetric divisions of a single sensory organ precursor (SOP). Despite a number of mutational studies investigating the regulation of ORN development, a majority of the transcriptional programs that lead to the different ORN classes in the developing olfactory system are unknown. Here we use transcriptional profiling across the time series of antennal development to identify novel transcriptional programs governing the differentiation of ORNs. We surveyed four critical developmental stages of the olfactory system: 3rd instar larval (prepatterning), 8 hours after puparium formation (APF, SOP selection), 40 hrs APF (neurogenesis), and adult antennae. We focused on the expression profiles of olfactory receptor genes and transcription factors—the two main classes of genes that regulate the sensory identity of ORNs. We identify distinct clusters of genes that have overlapping temporal expression profiles suggesting they have a key role during olfactory system development. We show that the expression of the transcription factor distal antenna (dan) is highly similar to other prepatterning factors and is required for the expression of a subset of ORs. |
format | Online Article Text |
id | pubmed-5244397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52443972017-01-23 Transcriptional profiling of olfactory system development identifies distal antenna as a regulator of subset of neuronal fates Barish, Scott Li, Qingyun Pan, Jia W. Soeder, Charlie Jones, Corbin Volkan, Pelin C. Sci Rep Article Drosophila uses 50 different olfactory receptor neuron (ORN) classes that are clustered within distinct sensilla subtypes to decipher their chemical environment. Each sensilla subtype houses 1–4 ORN identities that arise through asymmetric divisions of a single sensory organ precursor (SOP). Despite a number of mutational studies investigating the regulation of ORN development, a majority of the transcriptional programs that lead to the different ORN classes in the developing olfactory system are unknown. Here we use transcriptional profiling across the time series of antennal development to identify novel transcriptional programs governing the differentiation of ORNs. We surveyed four critical developmental stages of the olfactory system: 3rd instar larval (prepatterning), 8 hours after puparium formation (APF, SOP selection), 40 hrs APF (neurogenesis), and adult antennae. We focused on the expression profiles of olfactory receptor genes and transcription factors—the two main classes of genes that regulate the sensory identity of ORNs. We identify distinct clusters of genes that have overlapping temporal expression profiles suggesting they have a key role during olfactory system development. We show that the expression of the transcription factor distal antenna (dan) is highly similar to other prepatterning factors and is required for the expression of a subset of ORs. Nature Publishing Group 2017-01-19 /pmc/articles/PMC5244397/ /pubmed/28102318 http://dx.doi.org/10.1038/srep40873 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Barish, Scott Li, Qingyun Pan, Jia W. Soeder, Charlie Jones, Corbin Volkan, Pelin C. Transcriptional profiling of olfactory system development identifies distal antenna as a regulator of subset of neuronal fates |
title | Transcriptional profiling of olfactory system development identifies distal antenna as a regulator of subset of neuronal fates |
title_full | Transcriptional profiling of olfactory system development identifies distal antenna as a regulator of subset of neuronal fates |
title_fullStr | Transcriptional profiling of olfactory system development identifies distal antenna as a regulator of subset of neuronal fates |
title_full_unstemmed | Transcriptional profiling of olfactory system development identifies distal antenna as a regulator of subset of neuronal fates |
title_short | Transcriptional profiling of olfactory system development identifies distal antenna as a regulator of subset of neuronal fates |
title_sort | transcriptional profiling of olfactory system development identifies distal antenna as a regulator of subset of neuronal fates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244397/ https://www.ncbi.nlm.nih.gov/pubmed/28102318 http://dx.doi.org/10.1038/srep40873 |
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