University Medical Center Groningen and University of Groningen, Department of Otorhinolaryngology and Head/Neck Surgery, 9713GZ Groningen, the Netherlands.
University Medical Center Groningen and University of Groningen, Department of Otorhinolaryngology and Head/Neck Surgery, 9713GZ Groningen, the Netherlands.
Curr Biol. 2020 Nov 16;30(22):4329-4341.e4. doi: 10.1016/j.cub.2020.08.035. Epub 2020 Sep 3.
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.
裸鼹鼠是高度发声、群居、穴居的啮齿动物,听觉却出人意料地差。导致它们听力改变的原因尚不清楚。此外,它们的听力改变是退化的还是适应其独特生活方式的,这是有争议的。我们使用各种方法来确定导致裸鼹鼠和相关的达马拉兰鼹鼠听力改变的因素,并研究这些改变是否是由放松或适应性选择引起的。值得注意的是,尽管从裸鼹鼠分离出的外毛细胞中 prestin 功能正常,但我们发现这两个物种都没有耳蜗放大。相反,耳蜗放大的缺失似乎是由于在这两个物种中观察到的毛束形态异常所致。通过利用精心管理的耳聋表型-基因型数据库,我们鉴定出与毛束形态异常和听力敏感度降低一致的氨基酸取代。在六个毛束连接蛋白中,发现了独特的氨基酸取代。分子进化分析显示,这六个毛束连接蛋白中的五个在基因和密码子水平上的选择压力都发生了变化。这三个蛋白中的三个取代与听力改变有关。总之,我们的研究结果确定了非洲鼹鼠听力改变的可能机制,使它们成为唯一被确定的自然缺乏耳蜗放大的哺乳动物。此外,我们的研究结果表明,非洲鼹鼠的听力改变是适应性的,可能是为了适应群居和穴居的生活方式。最后,我们的工作揭示了非洲鼹鼠听觉的多种独特进化轨迹,并将物种成员确立为自然发生的疾病模型,以研究人类听力损失。