Functional, Morphological, and Evolutionary Characterization of Hearing in Subterranean, Eusocial African Mole-Rats

Naked mole-rats are highly vocal, eusocial, subterranean rodents with, counterintuitively, poor hearing. The causes underlying their altered hearing are unknown. Moreover, whether altered hearing is degenerate or adaptive to their unique lifestyles is controversial. We used various methods to identi...

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Veröffentlicht in:Current biology 2020-11, Vol.30 (22), p.4329-4341.e4
Hauptverfasser: Pyott, Sonja J., van Tuinen, Marcel, Screven, Laurel A., Schrode, Katrina M., Bai, Jun-Ping, Barone, Catherine M., Price, Steven D., Lysakowski, Anna, Sanderford, Maxwell, Kumar, Sudhir, Santos-Sacchi, Joseph, Lauer, Amanda M., Park, Thomas J.
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container_end_page 4341.e4
container_issue 22
container_start_page 4329
container_title Current biology
container_volume 30
creator Pyott, Sonja J.
van Tuinen, Marcel
Screven, Laurel A.
Schrode, Katrina M.
Bai, Jun-Ping
Barone, Catherine M.
Price, Steven D.
Lysakowski, Anna
Sanderford, Maxwell
Kumar, Sudhir
Santos-Sacchi, Joseph
Lauer, Amanda M.
Park, Thomas J.
description Naked mole-rats are highly vocal, eusocial, subterranean rodents with, counterintuitively, poor hearing. The causes underlying their altered hearing are unknown. Moreover, whether altered hearing is degenerate or adaptive to their unique lifestyles is controversial. We used various methods to identify the factors contributing to altered hearing in naked and the related Damaraland mole-rats and to examine whether these alterations result from relaxed or adaptive selection. Remarkably, we found that cochlear amplification was absent from both species despite normal prestin function in outer hair cells isolated from naked mole-rats. Instead, loss of cochlear amplification appears to result from abnormal hair bundle morphologies observed in both species. By exploiting a well-curated deafness phenotype-genotype database, we identified amino acid substitutions consistent with abnormal hair bundle morphology and reduced hearing sensitivity. Amino acid substitutions were found in unique groups of six hair bundle link proteins. Molecular evolutionary analyses revealed shifts in selection pressure at both the gene and the codon level for five of these six hair bundle link proteins. Substitutions in three of these proteins are associated exclusively with altered hearing. Altogether, our findings identify the likely mechanism of altered hearing in African mole-rats, making them the only identified mammals naturally lacking cochlear amplification. Moreover, our findings suggest that altered hearing in African mole-rats is adaptive, perhaps tailoring hearing to eusocial and subterranean lifestyles. Finally, our work reveals multiple, unique evolutionary trajectories in African mole-rat hearing and establishes species members as naturally occurring disease models to investigate human hearing loss. [Display omitted] •Hearing is comparatively poor in African naked and Damaraland mole-rats•These mole-rats lack cochlear amplification and have disrupted hair bundles•Hair bundle proteins bear deafness-associated amino acid substitutions•Positive selection in some bundle proteins suggests altered hearing is adaptive Pyott et al. attribute comparatively poor hearing in African naked and Damaraland mole-rats to lack of cochlear amplification, disrupted hair bundles, and hair bundle proteins bearing deafness-associated amino acid substitutions. Positive selection in some bundle proteins suggests altered hearing is adaptive to subterranean and eusocial lifestyles.
doi_str_mv 10.1016/j.cub.2020.08.035
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The causes underlying their altered hearing are unknown. Moreover, whether altered hearing is degenerate or adaptive to their unique lifestyles is controversial. We used various methods to identify the factors contributing to altered hearing in naked and the related Damaraland mole-rats and to examine whether these alterations result from relaxed or adaptive selection. Remarkably, we found that cochlear amplification was absent from both species despite normal prestin function in outer hair cells isolated from naked mole-rats. Instead, loss of cochlear amplification appears to result from abnormal hair bundle morphologies observed in both species. By exploiting a well-curated deafness phenotype-genotype database, we identified amino acid substitutions consistent with abnormal hair bundle morphology and reduced hearing sensitivity. Amino acid substitutions were found in unique groups of six hair bundle link proteins. Molecular evolutionary analyses revealed shifts in selection pressure at both the gene and the codon level for five of these six hair bundle link proteins. Substitutions in three of these proteins are associated exclusively with altered hearing. Altogether, our findings identify the likely mechanism of altered hearing in African mole-rats, making them the only identified mammals naturally lacking cochlear amplification. Moreover, our findings suggest that altered hearing in African mole-rats is adaptive, perhaps tailoring hearing to eusocial and subterranean lifestyles. Finally, our work reveals multiple, unique evolutionary trajectories in African mole-rat hearing and establishes species members as naturally occurring disease models to investigate human hearing loss. [Display omitted] •Hearing is comparatively poor in African naked and Damaraland mole-rats•These mole-rats lack cochlear amplification and have disrupted hair bundles•Hair bundle proteins bear deafness-associated amino acid substitutions•Positive selection in some bundle proteins suggests altered hearing is adaptive Pyott et al. attribute comparatively poor hearing in African naked and Damaraland mole-rats to lack of cochlear amplification, disrupted hair bundles, and hair bundle proteins bearing deafness-associated amino acid substitutions. 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The causes underlying their altered hearing are unknown. Moreover, whether altered hearing is degenerate or adaptive to their unique lifestyles is controversial. We used various methods to identify the factors contributing to altered hearing in naked and the related Damaraland mole-rats and to examine whether these alterations result from relaxed or adaptive selection. Remarkably, we found that cochlear amplification was absent from both species despite normal prestin function in outer hair cells isolated from naked mole-rats. Instead, loss of cochlear amplification appears to result from abnormal hair bundle morphologies observed in both species. By exploiting a well-curated deafness phenotype-genotype database, we identified amino acid substitutions consistent with abnormal hair bundle morphology and reduced hearing sensitivity. Amino acid substitutions were found in unique groups of six hair bundle link proteins. Molecular evolutionary analyses revealed shifts in selection pressure at both the gene and the codon level for five of these six hair bundle link proteins. Substitutions in three of these proteins are associated exclusively with altered hearing. Altogether, our findings identify the likely mechanism of altered hearing in African mole-rats, making them the only identified mammals naturally lacking cochlear amplification. Moreover, our findings suggest that altered hearing in African mole-rats is adaptive, perhaps tailoring hearing to eusocial and subterranean lifestyles. Finally, our work reveals multiple, unique evolutionary trajectories in African mole-rat hearing and establishes species members as naturally occurring disease models to investigate human hearing loss. 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source Cell Press Free Archives; ScienceDirect Journals (5 years ago - present); EZB-FREE-00999 freely available EZB journals
subjects adaptive
auditory outer hair cells
cochlea
cochlear amplifier
deafness
evolution
hair bundle
prestin
selection
stereocilia
title Functional, Morphological, and Evolutionary Characterization of Hearing in Subterranean, Eusocial African Mole-Rats
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