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Homeostatic maintenance and age-related functional decline in the Drosophila ear
Age-related hearing loss (ARHL) is a threat to future human wellbeing. Multiple factors contributing to the terminal auditory decline have been identified; but a unified understanding of ARHL - or the homeostatic maintenance of hearing before its breakdown - is missing. We here present an in-depth a...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198581/ https://www.ncbi.nlm.nih.gov/pubmed/32366993 http://dx.doi.org/10.1038/s41598-020-64498-z |
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author | Keder, Alyona Tardieu, Camille Malong, Liza Filia, Anastasia Kashkenbayeva, Assel Newton, Fay Georgiades, Marcos Gale, Jonathan E. Lovett, Michael Jarman, Andrew P. Albert, Joerg T. |
author_facet | Keder, Alyona Tardieu, Camille Malong, Liza Filia, Anastasia Kashkenbayeva, Assel Newton, Fay Georgiades, Marcos Gale, Jonathan E. Lovett, Michael Jarman, Andrew P. Albert, Joerg T. |
author_sort | Keder, Alyona |
collection | PubMed |
description | Age-related hearing loss (ARHL) is a threat to future human wellbeing. Multiple factors contributing to the terminal auditory decline have been identified; but a unified understanding of ARHL - or the homeostatic maintenance of hearing before its breakdown - is missing. We here present an in-depth analysis of homeostasis and ageing in the antennal ears of the fruit fly Drosophila melanogaster. We show that Drosophila, just like humans, display ARHL. By focusing on the phase of dynamic stability prior to the eventual hearing loss we discovered a set of evolutionarily conserved homeostasis genes. The transcription factors Onecut (closest human orthologues: ONECUT2, ONECUT3), Optix (SIX3, SIX6), Worniu (SNAI2) and Amos (ATOH1, ATOH7, ATOH8, NEUROD1) emerged as key regulators, acting upstream of core components of the fly’s molecular machinery for auditory transduction and amplification. Adult-specific manipulation of homeostatic regulators in the fly’s auditory neurons accelerated - or protected against - ARHL. |
format | Online Article Text |
id | pubmed-7198581 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71985812020-05-08 Homeostatic maintenance and age-related functional decline in the Drosophila ear Keder, Alyona Tardieu, Camille Malong, Liza Filia, Anastasia Kashkenbayeva, Assel Newton, Fay Georgiades, Marcos Gale, Jonathan E. Lovett, Michael Jarman, Andrew P. Albert, Joerg T. Sci Rep Article Age-related hearing loss (ARHL) is a threat to future human wellbeing. Multiple factors contributing to the terminal auditory decline have been identified; but a unified understanding of ARHL - or the homeostatic maintenance of hearing before its breakdown - is missing. We here present an in-depth analysis of homeostasis and ageing in the antennal ears of the fruit fly Drosophila melanogaster. We show that Drosophila, just like humans, display ARHL. By focusing on the phase of dynamic stability prior to the eventual hearing loss we discovered a set of evolutionarily conserved homeostasis genes. The transcription factors Onecut (closest human orthologues: ONECUT2, ONECUT3), Optix (SIX3, SIX6), Worniu (SNAI2) and Amos (ATOH1, ATOH7, ATOH8, NEUROD1) emerged as key regulators, acting upstream of core components of the fly’s molecular machinery for auditory transduction and amplification. Adult-specific manipulation of homeostatic regulators in the fly’s auditory neurons accelerated - or protected against - ARHL. Nature Publishing Group UK 2020-05-04 /pmc/articles/PMC7198581/ /pubmed/32366993 http://dx.doi.org/10.1038/s41598-020-64498-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Keder, Alyona Tardieu, Camille Malong, Liza Filia, Anastasia Kashkenbayeva, Assel Newton, Fay Georgiades, Marcos Gale, Jonathan E. Lovett, Michael Jarman, Andrew P. Albert, Joerg T. Homeostatic maintenance and age-related functional decline in the Drosophila ear |
title | Homeostatic maintenance and age-related functional decline in the Drosophila ear |
title_full | Homeostatic maintenance and age-related functional decline in the Drosophila ear |
title_fullStr | Homeostatic maintenance and age-related functional decline in the Drosophila ear |
title_full_unstemmed | Homeostatic maintenance and age-related functional decline in the Drosophila ear |
title_short | Homeostatic maintenance and age-related functional decline in the Drosophila ear |
title_sort | homeostatic maintenance and age-related functional decline in the drosophila ear |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198581/ https://www.ncbi.nlm.nih.gov/pubmed/32366993 http://dx.doi.org/10.1038/s41598-020-64498-z |
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