Homeostatic maintenance and age-related functional decline in the Drosophila ear

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作者
Alyona Keder
Camille Tardieu
Liza Malong
Anastasia Filia
Assel Kashkenbayeva
Fay Newton
Marcos Georgiades
Jonathan E. Gale
Michael Lovett
Andrew P. Jarman
Joerg T. Albert
机构
[1] Ear Institute,
[2] University College London,undefined
[3] 332 Gray’s Inn Road,undefined
[4] National Heart and Lung Institute,undefined
[5] Imperial College London,undefined
[6] Guy Scadding Building,undefined
[7] Dovehouse Street,undefined
[8] Centre for Discovery Brain Sciences,undefined
[9] Edinburgh Medical School,undefined
[10] University of Edinburgh,undefined
[11] Centre for Mathematics and Physics in the Life Sciences and Experimental Biology (CoMPLEX),undefined
[12] University College London,undefined
[13] Gower Street,undefined
[14] The Francis Crick Institute,undefined
[15] 1 Midland Road,undefined
[16] Department of Cell and Developmental Biology,undefined
[17] University College London,undefined
[18] Gower Street,undefined
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摘要
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.
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