Abstract

The mammalian inner ear has a limited capacity to regenerate its mechanosensory hair cells. This lack of regenerative capacity underlies the high incidence of age-related hearing loss in humans. In contrast, non-mammalian vertebrates can form new hair cells when damage occurs, a mechanism that depends on re-activation of expression of the pro-hair cell transcription factor Atoh1. Here, we show that members of the E2F transcription factor family, known to play a key role in cell cycle progression, regulate the expression of Atoh1. E2F1 activates chicken Atoh1 by directly interacting with a cis-regulatory region distal to the avian Atoh1 gene. E2F does not activate mouse Atoh1 gene expression, since this regulatory element is absent in mammals. We also show that E2F1 expression changes dynamically in the chicken auditory epithelium during ototoxic damage and hair cell regeneration. Therefore, we propose a model in which the mitotic regeneration of non-mammalian hair cells is due to E2F1-mediated activation of Atoh1 expression, a mechanism which has been lost in mammals.

Highlights

  • The mammalian inner ear has a limited capacity to regenerate its mechanosensory hair cells

  • We show that E2F1 expression changes dynamically in the chicken auditory epithelium during ototoxic damage and hair cell regeneration

  • The regulation of mammalian ATOH1 expression has previously been shown to be controlled by two evolutionary conserved regions (ECRs) downstream of the Atoh[1] locus which are sufficient to drive the expression of an Atoh1/lacZ reporter and replicate in most of the tissue specific expression of ­ATOH124,26

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Summary

Introduction

The mammalian inner ear has a limited capacity to regenerate its mechanosensory hair cells This lack of regenerative capacity underlies the high incidence of age-related hearing loss in humans. The inability to regenerate HCs when they are lost due to the effects of ototoxic agents, noise or ageing is a major cause of sensory hearing loss in humans. The reasons for the limited capacity for HC regeneration in the vestibular organs of mammals and its complete absence in the organ of Corti are unknown, but could be due in part to the inability of adult mammalian SCs to re-activate Atoh[1] expression after HC loss. Therapies requires a better understanding of the factors acting upstream of, or in conjunction with, Atoh[1] to initiate a complete regenerative response in non-mammalian species

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