For echolocating bats, hearing is essential for survival. Specializations for detecting and processing high frequency sounds are apparent throughout their auditory systems. Recent studies on echolocating mammals have reported evidence of parallel evolution in some hearing-related genes in which distantly related groups of echolocating animals (bats and toothed whales), cluster together in gene trees due to apparent amino acid convergence. However, molecular adaptations can occur not only in coding sequences, but also in the regulation of gene expression. The aim of this study was to examine the expression of hearing-related genes in the inner ear of developing big brown bats, Eptesicus fuscus, during the period in which echolocation vocalizations increase dramatically in frequency. We found that seven genes were significantly upregulated in juveniles relative to adults, and that the expression of four genes through development correlated with estimated age. Compared to available data for mice, it appears that expression of some hearing genes is extended in juvenile bats. These results are consistent with a prolonged growth period required to develop larger cochlea relative to body size, a later maturation of high frequency hearing, and a greater dependence on high frequency hearing in echolocating bats.
Citation: Mao B, Moss CF, Wilkinson GS (2017) Age-dependent gene expression in the inner ear of big brown bats (Eptesicus fuscus). PLoS ONE 12(10): e0186667. https://doi.org/10.1371/journal.pone.0186667
Editor: Michael Smotherman, Texas A&M University College Station, UNITED STATES
Received: June 4, 2017; Accepted: October 5, 2017; Published: October 26, 2017
Copyright: © 2017 Mao et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: B.M. was supported on training grant No. T32 DC000046 from the National Institute of Deafness and Communicative Disorders of the National Institutes of Health (https://www.nidcd.nih.gov/), awarded to A. N. Popper. Partial funding for open access provided by the UMD Libraries' Open Access Publishing Fund. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Echolocating bats have among the highest frequency hearing in the animal kingdom . While high frequency hearing confers a survival benefit to many animals, it is essential for the survival of bats, because they rely on echolocation to avoid obstacles, obtain food, and find roosts and conspecifics. High frequencies also allow bats to control the directionality of calls , , determine distance to targets , reject non-target echo clutter , and resolve fine spatial details such as shape, size, and texture [6–8]. Furthermore, bats are exceptionally long-lived for their size, with individuals of some species living more than 30 years . The need for echolocation throughout life suggests that the ability to hear high frequencies without severe age-related deterioration may have been under positive selection in echolocating bats. This stands in contrast with the occurrence of age-related hearing loss (presbycusis) in humans, which has been estimated to be 40% among those over 70 .
The importance of hearing to echolocators has been illustrated by a number of recent studies examining the molecular evolution of genes involved in hearing in bats. Several genes known from human and mouse studies to be crucial for normal hearing, such as transmembrane channel-like 1 (Tmc1) and Prestin/SLC26A5, exhibit convergence between the two distantly related groups of echolocating bats, or even between echolocating bats and whales, such that gene trees sometimes group echolocators together to the exclusion of non-echolocators [11–17]. While the results of these studies are compelling, the amount or timing of gene expression may also contribute to different phenotypes without requiring changes in coding sequence. Recent studies have shown that changes in gene regulation can influence the physical differences between bats and other mammals: transgenic mice possessing bat limb enhancers exhibit prolonged expression of limb elongation genes  and develop significantly longer limbs than control mice .
The big brown bat (Eptesicus fuscus) is an insectivore that hunts in edge spaces between open and cluttered environments . This behavior requires the disambiguation of cascades of echoes from multiple objects into separate percepts [21–22], which must occur quickly enough to inform motor decisions in flight. Because echolocation and flight are critical for a young bat’s survival, the development of hearing occurs concurrently with echolocation calls and the motor skills involved in flight [23–28]. The echolocation calls of juvenile big brown bats undergo significant changes between birth and three weeks of age, becoming shorter in duration and higher in frequency [26–29]. These changes in echolocation call frequencies likely coincide with changes in their hearing, because the frequency place map of the cochlea changes as it matures, with higher frequency hearing developing later [30, 31]. Additionally, the call frequencies of five species of bats were lower in the first year of life than later in adulthood, suggesting that fine-tuning of echolocation calls may occur well after the development of hearing is complete (summarized in ).
Because of their dependence on hearing for survival and their relatively well-developed auditory systems, echolocating bats provide a valuable opportunity to examine postnatal hearing development in an auditory specialist. Laryngeally echolocating bats possess larger cochlea  relative to basicranial width than non-echolocating or non-laryngeally echolocating bats . Bats using constant-frequency calls also exhibit overrepresentation of dominant call frequencies in basilar membrane (BM) dimensions and spiral ganglion density , and extremely short hair cells and stereocilia . A recent study showed that echolocating bats sustain a high prenatal cochlear growth rate throughout development compared to non-echolocating bats and other mammals , but which genes change expression during bat cochlear development is unknown. Here, we report on the expression of selected hearing-related genes in the inner ears of young big brown bats over a two-week period during which their calls rapidly increase in frequency, becoming more similar to adult echolocation calls [26–29]. Because these pronounced frequency shifts in vocalizations have been reported to coincide with frequency shifts in hearing in several bat species (e.g., [24, 38, 39]), examining gene expression during this period may provide insight into the regulatory changes associated with the development of high frequency hearing.
Materials and methods
Subjects and sample preparation
Pregnant female Eptesicus fuscus were captured in the wild under a permit from the Maryland Department of Natural Resources. All twelve juvenile subjects were born in captivity. Because they were group-housed and cluster together, exact dates of birth could not be directly recorded. Instead, forearm length was measured with calipers and used to estimate age . Forearm length is a more accurate age estimator than mass for big brown bats, and results from formulae relating forearm length to age do not differ between wild and captive bats . Estimated ages ranged from postnatal day (PND) 9 to 19. Juveniles were weighed, anesthetized with isoflurane and euthanized via decapitation. All procedures were in accordance with the National Institutes of Health’s Guide for the Care and Use of Laboratory Animals, and were approved by the Johns Hopkins University Institutional Animal Care and Use Committee (protocol BA14A111). Samples were also obtained from two adult individuals under a protocol approved by the University of Maryland Institutional Animal Care and Use Committee (R-13-76).
Inner ear samples, consisting of the entire otic capsule (both cochleae and vestibular organs), were collected immediately post-mortem and placed into liquid nitrogen prior to storage at -80°C until extraction. Both left and right cochleae from an individual were pooled and processed together. Samples were homogenized with a mortar and pestle while submerged in liquid nitrogen. RNA extraction was performed using a mirVana kit (Ambion), with added proteinase K (Sigma Aldrich) to improve yield . All samples were treated with TURBO DNA-free DNAse (Ambion) and cleaned with isopropanol and ethanol. Sample quality was checked on a Nanodrop spectrophotometer and reverse transcribed with M-MLV (Thermo Fisher) using a 50/50 mix of oligo-dT and random primers to lower the risk of bias or truncated transcripts associated with a single priming method [42, 43].
Gene selection and primer design
Candidate genes were selected based on one or more of the following criteria: upregulated in an echolocating bat vs. a non-echolocating bat (e.g., ); upregulated in an adult mouse relative to juvenile mouse (e.g., ); expressed in mid- to late- development (e.g., ); evidence of parallel or convergent evolution between echolocating bats and whales (e.g., ); evidence of parallel or convergent evolution between distantly related echolocating bats (e.g., ); or involved in formation of essential cochlear structures (e.g., ; Table 1). For each gene, all available mRNA transcripts from Eptesicus fuscus and all bats of the genus Myotis (another genus in the same family, Vespertilionidae), were downloaded from GenBank (NCBI) and aligned using Clustal Omega (EMBL-EBI). Sequences from Myotis spp. were included in order to reduce the risk of designing primers in regions with polymorphic sites. All primer pairs were designed within the same exon to permit preliminary testing on genomic DNA.
In the “Criteria for inclusion column,” letter codes mean the following: A, upregulated in an echolocating bat vs. a non-echolocating bat; B, upregulated in an adult mouse relative to juvenile mouse; C, expressed in mid- to late- development; D, exhibits signs of parallel or convergent evolution between echolocating bats and whales; E, exhibits signs of parallel or convergent evolution between distantly related echolocating bats; F, participates in forming essential cochlear structures. aMutations in Gjb6 may cause hearing loss by inducing a downregulation of Gjb2. Gjb6 appears not be critical for hearing, unlike Gjb2 (see ).
To identify exons in an Eptesicus fuscus transcript, exonic regions of the Myotis lucifugus transcript, as identified in Ensembl, were blasted against the transcript for Eptesicus fuscus. If the Myotis transcript was not available in Ensembl, the mouse (Mus musculus) transcript was used instead. If the exonic region was conserved among Eptesicus and Myotis spp., it was entered into Primer-BLAST (NCBI). Potential primer pairs were checked for specificity against Eptesicus fuscus RefSeq data, potential for cross- and self-dimerization, and potential to form hairpins using Beacon Designer (Premier Biosoft). Only primers that were 100% conserved across all known transcripts from Eptesicus and Myotis spp. were used for quantitative PCR. Primer sequences are given in Table 2.
Efficiencies greater than 100% typically indicate the presence of inhibitors, the effects of which decrease at lower dilutions.
Five-point dilution series (1:3 or 1:4) were performed for each gene and only primer pairs with efficiencies greater than 90% after exclusion of non-linear dilutions (typically at the highest or lowest concentration of template) were selected for use. Post-amplification melt curves were checked to ensure each product consisted of a single, narrow peak, and gel electrophoresis was performed for each amplicon to ensure a single product of correct size was produced during amplification.
qPCR and data analysis
For each primer pair, 20 μL reactions were prepared for each of the samples in triplicate using SYBR Select Master Mix (Thermo Fisher). Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was included as a reference gene on each 96-well plate. Fluorescence was measured using a Roche 480 Lightcycler and melt curves were measured immediately after the completion of all amplification cycles. Technical replicates that reached threshold two or more cycles earlier or later than the other two replicates were excluded from analyses.
For each sample-primer combination on a given plate, the comparative CT method  was used to calculate relative expression. Briefly, delta CT was calculated as the average threshold cycle of replicates from the gene of interest minus the average threshold cycle of the GAPDH replicates. To control for any batch effects, delta CT values were adjusted by the difference in mean delta CT between batches for each gene. Delta CT values were then normalized by subtracting the average delta CT for all juvenile samples for a given gene (yielding delta-delta CT). Fold expression was calculated as the efficiency-adjusted amplification factor raised to the negative delta-delta CT. Average CT and calculated fold expression values are given in S1 Table.
We performed t-tests to determine whether the mean adjusted fold expression values of juveniles differed from adults for 13 genes. We also fitted least squares regression lines between estimated age and adjusted fold change to identify genes that exhibited age-dependent expression. All statistical analyses were performed in JMP 13.0.0 (SAS Institute). Figures were generated in JMP and MATLAB R2015a (The Mathworks).
Adult vs. juvenile expression
Of the 13 genes tested, eight exhibited differential expression between juveniles and adults (Table 3; Fig 1). Expression was higher in adults for six genes—bone morphogenic protein 7 (Bmp7), carcinoembryonic antigen-related cell adhesion molecule 16 (Ceacam16), collagen type XI alpha 2 chain (Col11A2), POU class 4 transcription factor 3 (Pou4f3), transmembrane channel-like 2 (Tmc2), and USH1 protein network component harmonin (Ush1C), and higher in juveniles for the remaining two genes—gap junction protein beta 2 (Gjb2) and POU class 3 transcription factor 4 (Pou3f4).
Values were adjusted to remove the effect of batch and normalized to average juvenile expression (see Materials and Methods). Juvenile data are shown in light grey, and adult data are shown in dark grey. Asterisks denote level of significance of associated t-tests (see Table 3; *p≤0.05, **p≤0.01, ***p≤0.005).
For all t-tests, there were 13 degrees of freedom, and bivariate fits had 11 degrees of freedom. Fold change values were adjusted to the mean of all juvenile samples and also to differences in mean juvenile expression between batches (see Materials and Methods). Asterisks denote level of significance (*p≤0.05, **p≤0.01, ***p≤0.005).
Age-related gene expression
Linear fits of adjusted fold change to estimated age revealed that juvenile age over a two-week period predicted expression for four genes: POU class 3 transcription factor 4 (Pou3f4), transmembrane channel-like 1 (Tmc1), and gap junction protein beta 2 (Gjb2) and 6 (Gjb6; Table 3; Fig 2).
Values were normalized to average juvenile expression and adjusted to remove the effect of batch (see Materials and Methods). Asterisks denote level of significance of associated t-tests (see Table 3; *p≤0.05, **p≤0.01, ***p≤0.005).
Adult vs. juvenile expression
We found significant differences between juvenile and adult bat in inner ear expression of eight genes. The most significantly upregulated gene in adults was Tmc2 (Fig 1). Tmc1 and Tmc2 are expressed in the cochlea and vestibular system [72, 74], and encode components of the mechanoelectrotransduction (MET) channels of hair cells . Their protein products may form heteromeric assemblies that confer different electrophysiological properties to hair cells along the BM . Despite functional redundancy between Tmc1 and Tmc2, mice with a targeted deletion of Tmc1 are deaf because Tmc2 does not persist in the cochlea beyond early postnatal ages . In the utricle, Tmc1 and Tmc2 expression continues through the first few postnatal weeks . These observations in postnatal mice suggest that continued Tmc2 expression into adulthood in bats may be restricted to the balance organs.
Bmp7, Ceacam16, Col11A2, and Ush1C were also upregulated in adults relative to juveniles (Fig 1). Bmp7 is expressed in a gradient along the basilar papilla, and disruption of this gradient results in loss of tonotopy and morphological changes in sensory cells . While we found that it was upregulated in adult bats, another study reported that Bmp7 is downregulated in the cochlear sensory epithelia of P60 mice relative to P1 mice . Ush1C encodes a protein, harmonin, that is a component of upper tip-link densities of stereocilia bundles . Mutations in Ush1C are associated with Usher syndrome type 1C in humans , and mouse mutants exhibit splayed stereocilia bundles and progressive loss of hair cells and spiral ganglion neurons . Cochlear expression of Ush1C drops prior to birth and then increases into adulthood in mice  and is similarly expressed at higher levels in adult than juvenile bats (Table 3; Fig 1).
Both Ceacam16 and Col11A2 encode proteins that are components of the tectorial membrane (TM), and their deletion disrupts TM structure [53, 56], resulting in hearing loss [52, 54]. The TM acts as an inertial mass which allows the outer hair cells (OHCs) to amplify BM motion . Reducing its mass by deleting Tectb improved the frequency selectivity of the BM and neural response at high frequencies . Ceacam16 may stabilize interactions between TM glycoproteins, such that cochlear amplification becomes unstable without it . The upregulation of Col11A2 and Ceacam16 may, therefore, result in a TM structure which allows bat hair cells to effectively amplify high frequency sounds.
Pou4f3 showed the greatest difference in expression between age groups (Fig 1). Pou4f3 is a transcription factor implicated in progressive non-syndromic hearing loss in humans . Mice lacking Pou4f3 fail to develop stereocilia bundles , resulting in the loss of hair cells and spiral ganglion neurons . Pou4f3 is expressed into adulthood in mice [46, 70, 85] but is downregulated in the P60 mouse cochlea compared to P1 . Taken together, the upregulation of Tmc2, Bmp7, Ush1C, Ceacam16, Col11A2, and Pou4f3 in adult big brown bats may reflect continued development or maturation of the inner ear that continues beyond the time point at which bats can fly and produce adult-like echolocation calls. The two genes that were significantly upregulated in juveniles relative to adult bats, Gjb2 and Pou3f4, are discussed in further detail in the next section, as their expression also correlated with juvenile age.
Age-related gene expression
Four genes were significantly upregulated with age in juvenile bats. Of these, Gjb2, Gjb6, and Pou3f4 were downregulated in adult bats relative to juvenile bats, perhaps because their roles in inner ear development were complete (Table 3; Figs 1 and 2). The expression of the fourth gene, Tmc1, did not differ significantly between juveniles and adults, although standard errors for adult samples were high due in part to small sample size (Fig 1). While levels of the protein products (Cx26 and Cx30) of Gjb2 and Gjb6 saturate at P15 in the mouse cochlea , we found that Gjb2 and Gjb6 expression increased through the third postnatal week in the inner ears of bats. In an earlier report, these genes were significantly upregulated in the inner ears of an echolocating bat (Myotis ricketti) compared to a non-echolocating bat (Cynopterus sphinx) . Gjb2 appears critical for cochlear function and is implicated in the most common form of congenital deafness in humans [59, 87]. Gjb6 has also been linked to human deafness , although the deleterious effects of Gjb6 knockdown in mice are less severe than those of Gjb2 and may be partly caused by associated downregulation of Gjb2 [64, 88].
The upregulation of Gjb2 and Gjb6 may reflect greater numbers of gap junctions in the bat cochlea. Both genes may participate in the recycling of potassium, the major charge carrier in transduction (reviewed in ). Conditional knockdown of Gjb2 in early postnatal mice impaired OHC amplification and high frequency hearing , consistent with gap junction conductivity enabling OHCs to respond to higher frequencies [91–93]. The continued expression of Gjb2 and Gjb6 may also result from prolonged development of the cochleae, which are relatively large in echolocating bats [33, 34]. A recent paper showed that the relative median prenatal growth rate of echolocating bats’ cochleae was approximately two and four times larger, respectively, than that of non-echolocating mammals and non-laryngeally echolocating bats .
Gjb2 and Gjb6 upregulation may provide some protection against hearing loss in echolocating bats, which depend on hearing throughout their long lives. Conditional knockdown of Gjb2 in mice at P18 resulted in greater susceptibility to noise-induced hearing loss at P30 and P45 , and mice lacking Gjb6 exhibited abnormal epithelial repair after hair cell loss and reduced intercellular communication between supporting cells . Cx26 and Cx30 may be targets of oxidative damage, contributing to age-related and noise-induced hearing loss . The increase of Gjb2 and Gjb6 expression during juvenile development in bats may, therefore, be associated with a system of gap junctions that facilitates cochlear protection or repair. After an hour of broadband noise exposure at 152 dB SPL, adult big brown bats showed no significant threshold shifts [97, 98], increase in errors, or changes in echolocation behavior when flying through a cluttered corridor . Additionally, bat echolocation calls can be as intense as 140 dB, although they last only milliseconds , and it is unclear whether wild bats encounter sounds that could damage their hearing.
Pou3f4 is a transcription factor that has been implicated in X-linked non-syndromic deafness . Pou3f4 mouse mutants exhibit audiological and balance impairments, reduced coiling of the cochlea , and defects in gap junctions . Deletion of Pou3f4 from otic mesenchyme causes defasciculation of spiral ganglion neurons , which could disrupt coordination of hair cell and neuronal frequencies . These studies suggest that the continued upregulation of Pou3f4 in the developing bat inner ear may be linked to cochlear elongation and functional organization. One report did not find evidence of positive selection on Pou3f4 among echolocating bats , suggesting that change in expression, rather than sequence, has been more important in bats.
Tmc1 encodes a MET channel protein  that localizes to the tip-links of stereocilia  and which is essential for mechanotransduction in cochlear hair cells . Reports of its postnatal expression pattern conflict: one study found a slight increase, then decrease in Tmc1 expression in the inner ear of mice from P9 to P19, with a net decrease of approximately 8% over the period . Another study reported a 2-fold increase between P9 and P19 in the utricle and a much greater increase over the same time period in the apex of the cochlea . The increase in Tmc1 we observed in developing big brown bats is consistent with the latter study, and with a transcriptomic comparison of the inner ears of bats which showed that 18 hearing-related genes were upregulated in an echolocating bat compared to a non-echolocating bat, including Tmc1, which was also upregulated in echolocating bats relative to mice and rats .
Although the nature of our samples (entire inner ears) did not permit examination of gene expression specifically in the cochlea or its basal, high frequency region, the upregulation of Tmc1 could reflect a greater number of MET channels per hair cell, which might increase sensitivity to high frequencies by strengthening the influx of calcium and reducing the adaptation time of hair cells (reviewed in ). In midshipman fish (Porichthys notatus), fluctuations in the expression of a calcium-activated potassium (BK) channel conferred greater hearing sensitivity during the breeding season , and knockdown of BK channel genes increased thresholds in zebrafish larvae . Alternatively, bat MET channels may contain more Tmc1 subunits. Because mouse hair cells expressing only wildtype Tmc1 had faster adaptation times than those expressing only Tmc2 or only a Tmc1 mutant , MET channels incorporating more Tmc1 subunits might respond better at high frequencies.
Although only a small set of genes were examined in this study, and we did not manipulate gene expression directly and monitor subsequent phenotypic effects, this study provides the first insight into the developmental expression of hearing genes in echolocating animals. Without separation of the cochlea from the vestibular organs, it is not possible to ascribe expression differences to one section of the inner ear or the other. However, Tmc1 and Gjb2 mouse mutants exhibit hearing loss without vestibular dysfunction, illustrating their greater importance for audition [47, 60]. Furthermore, hearing genes exhibiting various degrees of convergence between echolocating bats and whales have been implicated in human deafness [11–17], as have most of the genes we identified as being significantly upregulated with age in big brown bats. In particular, Tmc1 exhibits both sequence convergence  and upregulation (, this report) in echolocators, suggesting that in some cases selection may act on both coding sequence and gene regulation to confer improved hearing in echolocating mammals.
Wei Xian provided logistical support in the procurement of samples, Josephine Reinhardt and Kimberly Paczolt offered advice on RNA extraction and qPCR, and the Moss and Wilkinson labs gave valuable feedback. Partial funding for open access provided by the UMD Libraries' Open Access Publishing Fund.
- 1. Heffner HE, Heffner RS. High-frequency hearing. In: Dallos P, Oertel D, Hoy R, editors. Handbook of the senses: Audition. New York, NY: Elsevier; 2008. pp. 55–60.
- 2. Hartley DJ, Suthers RA. The sound emission pattern of the echolocating bat, Eptesicus fuscus. J Acoust Soc Am. 1989;85: 1348–1351.
- 3. Surlykke A, Pedersen SB, Jakobsen L. Echolocating bats emit a highly directional sonar sound beam in the field. Proc R Soc Lond B. 2009;276: 853–860. pmid:19129126
- 4. Simmons JA. The resolution of target range by echolocating bats. J Acoust Soc Am. 1973;54: 157–173. pmid:4738624
- 5. Bates ME, Simmons JA, Zorikov TV. Bats use echo harmonic structure to distinguish their targets from background clutter. Science. 2011;333: 627–630. pmid:21798949
- 6. Simmons JA, Vernon JA. Echolocation: discrimination of targets by the bat, Eptesicus fuscus. J Exp Zool. 1971;176: 315–328. pmid:5548872
- 7. Habersetzer J, Vogler B. Discrimination of surface-structured targets by the echolocating bat Myotis myotis during flight. J Comp Physiol. 1983;152: 275–282.
- 8. Falk B, Williams T, Aytekin M, Moss CF. Adaptive behavior for texture discrimination by the free-flying big brown bat, Eptesicus fuscus. J Comp Physiol A. 2011;197: 491–503. pmid:21246202
- 9. Wilkinson GS, South JM. Life history, ecology and longevity in bats. Aging Cell. 2002;1: 124–131. pmid:12882342
- 10. Collins JG. Prevalence of selected chronic conditions: United States, 1990–1992. Hyattsville, MD: National Center for Health Statistics, Centers for Disease Control and Prevention; 1997.
- 11. Li G, Wang J, Rossiter SJ, Jones G, Cotton JA, Zhang S. The hearing gene Prestin reunites echolocating bats. PNAS. 2008;105: 13959–13964. pmid:18776049
- 12. Li Y, Liu Z, Shi P, Zhang J. The hearing gene Prestin unites echolocating bats and whales. Curr Biol. 2010;20: R55–R56. pmid:20129037
- 13. Liu Y, Rossiter SJ, Han X, Cotton JA, Zhang S. Cetaceans on a molecular fast track to ultrasonic hearing. Curr Biol. 2010;20: 1834–1839. pmid:20933423
- 14. Liu Z, Li S, Wang W, Xu D, Murphy RW, Shi P. Parallel evolution of KCNQ4 in echolocating bats. PLoS ONE. 2011;6: e26618. pmid:22046315
- 15. Liu Y, Han N, Franchini LF, Xu H, Pisciottano F, Elgoyhen AB, et al. The voltage-gated potassium channel subfamily KQT member 4 (KCNQ4) displays parallel evolution in echolocating bats. Mol Biol Evol. 2012;29: 1441–1450. pmid:22319145
- 16. Davies KTJ, Cotton JA, Kirwan JD, Teeling EC, Rossiter SJ. Parallel signatures of sequence evolution among hearing genes in echolocating mammals: an emerging model of genetic convergence. Heredity. 2012;108: 480–489. pmid:22167055
- 17. Shen Y-Y, Liang L, Li G-S, Murphy RW, Zhang Y-P. Parallel evolution of auditory genes for echolocation in bats and toothed whales. Zhang J, editor. PLoS Genet. 2012;8: e1002788. pmid:22761589
- 18. Booker BM, Friedrich T, Mason MK, VanderMeer JE, Zhao J, Eckalbar WL, et al. Bat accelerated regions identify a bat forelimb specific enhancer in the HoxD locus. Desplan C, editor. PLoS Genet. 2016;12: e1005738. pmid:27019019
- 19. Cretekos CJ, Wang Y, Green ED, Martin JF, Rasweiler JJ, Behringer RR. Regulatory divergence modifies limb length between mammals. Genes Dev. 2008;22: 141–151. pmid:18198333
- 20. Surlykke A, Moss CF. Echolocation behavior of big brown bats, Eptesicus fuscus, in the field and the laboratory. J Acoust Soc Am. 2000;108: 2419–2429. pmid:11108382
- 21. Moss CF, Surlykke A. Auditory scene analysis by echolocation in bats. Journal of the Acoustical Society of America. 2001;110: 2207–2226. pmid:11681397
- 22. Moss CF, Surlykke A. Probing the Natural Scene by Echolocation in Bats. Front Behav Neurosci. 2010;4. pmid:20740076
- 23. Buchler ER. The development of flight, foraging, and echolocation in the little brown bat (Myotis lucifugus). Behav Ecol Sociobiol. 1980;6: 211–218.
- 24. Rübsamen R. Ontogenesis of the echolocation system in the rufous horseshoe bat, Rhinolophus rouxi (Audition and vocalization in early postnatal development). J Comp Physiol. 1987;161: 899–913.
- 25. Powers LV, Kandarian SC, Kunz TH. Ontogeny of flight in the little brown bat, Myotis lucifugus: behavior, morphology, and muscle histochemistry. J Comp Physiol A. 1991;168: 675–685.
- 26. Moss CF. Ontogeny of vocal signals in the big brown bat, Eptesicus fuscus. In: Nachtigall PE, Moore PWB, editors. Animal Sonar. New York, NY: Plenum Press; 1988. pp. 115–120. https://doi.org/10.1007/978-1-4684-7493-0_13
- 27. Moss CF, Redish D, Gounden C, Kunz TH. Ontogeny of vocal signals in the little brown bat, Myotis lucifugus. Anim Behav. 1997;54: 131–141. pmid:9268443
- 28. Mayberry HW, Faure PA. Morphological, olfactory, and vocal development in big brown bats. Biol Open. 2015;4: 22–34. pmid:25505151
- 29. Monroy JA, Carter ME, Miller KE, Covey E. Development of echolocation and communication vocalizations in the big brown bat, Eptesicus fuscus. J Comp Physiol A. 2011;197: 459–467. pmid:21327335
- 30. Harris DM, Dallos P. Ontogenetic changes in frequency mapping of a mammalian ear. Science. 1984;225: 741–743. pmid:6463651
- 31. Echteler SM, Arjmand E, Dallos P. Developmental alterations in the frequency map of the mammalian cochlea. Nature. 1989;341: 147–149. pmid:2779652
- 32. Jones G. The ontogeny of behaviour in bats: a functional perspective. In: Adams RA, Pedersen SC, editors. Ontogeny, functional ecology, and evolution of bats. Cambridge: Cambridge University Press; 2000. pp. 362–392.
- 33. Hsiao CJ, Jen PH-S, Wu CH. The cochlear size of bats and rodents derived from MRI images and histology. NeuroReport. 2015;26: 478–482. pmid:25919995
- 34. Kössl M, Vater M. Cochlear structure and function in bats. In: Popper AN, Fay RR, editors. Hearing by Bats. New York, NY: Springer; 1995. pp. 191–234. https://doi.org/10.1007/978-1-4612-2556-0_5
- 35. Kössl M, Vater M. The cochlear frequency map of the mustache bat, Pteronotus parnellii. J Comp Physiol A. 1985;157: 687–697. pmid:3837108
- 36. Vater M, Lenoir M. Ultrastructure of the horseshoe bat’s organ of corti. I. Scanning electron microscopy. J Comp Neurol. 1992;318: 367–379. pmid:1578008
- 37. Wang Z, Zhu T, Xue H, Fang N, Zhang J, Zhang L, et al. Prenatal development supports a single origin of laryngeal echolocation in bats. Nature Ecol Evol. 2017;1: 0021. pmid:28812602
- 38. Brown PE, Grinnell AD, Harrison JB. The development of hearing in the pallid bat, Antrozous pallidus. J Comp Physiol. 1978;126: 169–182.
- 39. Sterbing S. Postnatal development of vocalizations and hearing in the phyllostomid bat, Carollia perspicillata. J Mammal. 2002;83: 516–525.
- 40. Burnett CD, Kunz TH. Growth rates and age estimation in Eptesicus fuscus and comparison with Myotis lucifugus. J Mammal. 1982;63: 33–41.
- 41. Egyházi S, Bjöhle J, Skoog L, Huang F, Borg A-L, Frostvik Stolt M, et al. Proteinase K added to the extraction procedure markedly increases RNA yield from primary breast tumors for use in microarray studies. Clin Chem. 2004;50: 975–976. pmid:15105365
- 42. Nam DK, Lee S, Zhou G, Cao X, Wang C, Clark T, et al. Oligo(dT) primer generates a high frequency of truncated cDNAs through internal poly(A) priming during reverse transcription. Proc Natl Acad Sci. 2002;99: 6152–6156. pmid:11972056
- 43. Ståhlberg A, Håkansson J, Xian X, Semb H, Kubista M. Properties of the reverse transcription reaction in mRNA quantification. Clin Chem. 2004;50: 509–515. pmid:14726469
- 44. Dong D, Lei M, Liu Y, Zhang S. Comparative inner ear transcriptome analysis between the Rickett’s big-footed bats (Myotis ricketti) and the greater short-nosed fruit bats (Cynopterus sphinx). BMC Genomics. 2013;14: 1.
- 45. Smeti I, Assou S, Savary E, Masmoudi S, Zine A. Transcriptomic analysis of the developing and adult mouse cochlear sensory epithelia. Libby R, editor. PLoS ONE. 2012;7: e42987. pmid:22900075
- 46. Xiang M, Gao W-Q, Hasson T, Shin JJ. Requirement for Brn-3c in maturation and survival, but not in fate determination of inner ear hair cells. Development. 1998;125: 3935–3946. pmid:9735355
- 47. Kurima K, Peters LM, Yang Y, Riazuddin S, Ahmed ZM, Naz S, et al. Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function. Nature Genet. 2002;30: 277–284. pmid:11850618
- 48. Wyatt AW, Osborne RJ, Stewart H, Ragge NK. Bone morphogenetic protein 7 (BMP7) mutations are associated with variable ocular, brain, ear, palate, and skeletal anomalies. Hum Mut. 2010;31: 781–787. pmid:20506283
- 49. Mann ZF, Thiede BR, Chang W, Shin J-B, May-Simera HL, Lovett M, et al. A gradient of Bmp7 specifies the tonotopic axis in the developing inner ear. Nature Comm. 2014;5. pmid:24845721
- 50. Kammerer R, Zimmermann W. Coevolution of activating and inhibitory receptors within mammalian carcinoembryonic antigen families. BMC Biol. 2010;8: 1.
- 51. Zheng J, Miller KK, Yang T, Hildebrand MS, Shearer AE, DeLuca AP, et al. Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with -tectorin and is mutated in autosomal dominant hearing loss (DFNA4). Proc Natl Acad Sci. 2011;108: 4218–4223. pmid:21368133
- 52. Kammerer R, Ruttiger L, Riesenberg R, Schauble C, Krupar R, Kamp A, et al. Loss of mammal-specific tectorial membrane component carcinoembryonic antigen cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequencies. J Biol Chem. 2012;287: 21584–21598. pmid:22544735
- 53. Cheatham MA, Goodyear RJ, Homma K, Legan PK, Korchagina J, Naskar S, et al. Loss of the tectorial membrane protein CEACAM16 enhances spontaneous, stimulus-frequency, and transiently evoked otoacoustic emissions. J Neurosci. 2014;34: 10325–10338. pmid:25080593
- 54. McGuirt WT, Prasad SD, Griffith AJ, Kunst HP, Green GE, Shpargel KB, et al. Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13). Nature Genet. 1999;23: 413–419. pmid:10581026
- 55. Chen W. Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus. J Med Genet. 2005;42: e61–e61. pmid:16033917
- 56. Masaki K, Gu JW, Ghaffari R, Chan G, Smith RJH, Freeman DM, et al. Col11a2 deletion reveals the molecular basis for tectorial membrane mechanical anisotropy. Biophys J. 2009;96: 4717–4724. pmid:19486694
- 57. Rio C, Dikkes P, Liberman MC, Corfas G. Glial fibrillary acidic protein expression and promoter activity in the inner ear of developing and adult mice. J Comp Neurol. 2002;442: 156–162. pmid:11754168
- 58. Masuda M, Tanaka KF, Kanzaki S, Wakabayashi K, Oishi N, Suzuki T, et al. GFAP aggregates in the cochlear nerve increase the noise vulnerability of sensory cells in the organ of Corti in the murine model of Alexander disease. Neurosci Res. 2008;62: 15–24. pmid:18602179
- 59. Kelsell DP, Dunlop J, Stevens HP, Lench NJ, Liang JN, Parry G, et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature. 1997;387: 80–83. pmid:9139825
- 60. Cohen-Salmon M, Ott T, Michel V, Hardelin J-P, Perfettini I, Eybalin M, et al. Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death. Curr Biol. 2002;12: 1106–1111. pmid:12121617
- 61. Takada Y, Beyer LA, Swiderski DL, O’Neal AL, Prieskorn DM, Shivatzki S, et al. Connexin 26 null mice exhibit spiral ganglion degeneration that can be blocked by BDNF gene therapy. Hear Res. 2014;309: 124–135. pmid:24333301
- 62. Grifa A, Wagner CA, D’Ambrosio L, Melchionda S, Bernardi F, Lopez-Bigas N, et al. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus. Nature Genet. 1999;23: 16–18. pmid:10471490
- 63. Teubner B, Michel V, Pesch J, Lautermann J, Cohen-Salmon M, Söhl G, et al. Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential. Hum Mol Genet. 2003;12: 13–21. pmid:12490528
- 64. Boulay A-C, del Castillo FJ, Giraudet F, Hamard G, Giaume C, Petit C, et al. Hearing is normal without connexin30. J Neurosci. 2013;33: 430–434. pmid:23303923
- 65. Miwa T, Minoda R, Ise M, Yamada T, Yumoto E. Mouse otocyst transuterine gene transfer restores hearing in mice with connexin 30 deletion-associated hearing loss. Mol Ther. 2013;21: 1142–1150. pmid:23587925
- 66. Grillet N, Schwander M, Hildebrand MS, Sczaniecka A, Kolatkar A, Velasco J, et al. Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans. Am J Hum Genet. 2009;85: 328–337. pmid:19732867
- 67. de Kok YJ, van der Maarel SM, Bitner-Glindzicz M, Huber I, Monaco AP, Malcolm S, et al. Association between X-Linked mixed deafness and mutations in the POU domain gene POU3F4. Science. 1995;267: 685. pmid:7839145
- 68. Phippard D, Lu L, Lee D, Saunders JC, Crenshaw EB. Targeted mutagenesis of the POU-Domain gene Brn4/Pou3f4 causes developmental defects in the inner ear. J Neurosci. 1999;19: 5980–5989. pmid:10407036
- 69. Coate TM, Raft S, Zhao X, Ryan AK, Crenshaw EB, Kelley MW. Otic mesenchyme cells regulate spiral ganglion axon fasciculation through a Pou3f4/EphA4 signaling pathway. Neuron. 2012;73: 49–63. pmid:22243746
- 70. Xiang M, Gan L, Li D, Chen Z-Y, Zhou L, O’Malley BW, et al. Essential role of POU–domain factor Brn-3c in auditory and vestibular hair cell development. Proc Natl Acad Sci. 1997;94: 9445–9450. pmid:9256502
- 71. Vahava O, Morell R, Lynch ED, Weiss S, Kagan ME, Ahituv N, et al. Mutation in transcription factor POUF3 associated with inherited progressive hearing loss in humans. Science. 1998;279: 1950–1954. pmid:9506947
- 72. Kawashima Y, Géléoc GSG, Kurima K, Labay V, Lelli A, Asai Y, et al. Mechanotransduction in mouse inner ear hair cells requires transmembrane channel–like genes. J Clin Invest. 2011;121: 4796–4809. pmid:22105175
- 73. Pan B, Géléoc GS, Asai Y, Horwitz GC, Kurima K, Ishikawa K, et al. TMC1 and TMC2 are components of the mechanotransduction channel in hair cells of the mammalian inner ear. Neuron. 2013;79: 504–515. pmid:23871232
- 74. Kurima K, Ebrahim S, Pan B, Sedlacek M, Sengupta P, Millis BA, et al. TMC1 and TMC2 localize at the site of mechanotransduction in mammalian inner hair cell stereocilia. Cell Rep. 2015;12: 1606–1617. pmid:26321635
- 75. Steiner AB, Kim T, Cabot V, Hudspeth AJ. Dynamic gene expression by putative hair-cell progenitors during regeneration in the zebrafish lateral line. Proc Natl Acad Sci. 2014;111: E1393–E1401. pmid:24706895
- 76. Verpy E, Leibovici M, Zwaenepoel I, Liu X-Z, Gal A, Salem N, et al. A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C. Nature Genet. 2000;26: 51–55. pmid:10973247
- 77. Johnson KR, Gagnon LH, Webb LS, Peters LL, Hawes NL, Chang B, et al. Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene. Hum Mol Genet. 2003;12: 3075–3086. pmid:14519688
- 78. Grillet N, Xiong W, Reynolds A, Kazmierczak P, Sato T, Lillo C, et al. Harmonin mutations cause mechanotransduction defects in cochlear hair cells. Neuron. 2009;62: 375–387. pmid:19447093
- 79. Sanchez-Calderon H, Rodriguez-de la Rosa L, Milo M, Pichel JG, Holley M, Varela-Nieto I. RNA microarray analysis in prenatal mouse cochlea reveals novel IGF-I target genes: implication of MEF2 and FOXM1 transcription factors. Linden R, editor. PLoS ONE. 2010;5: e8699. pmid:20111592
- 80. Tian C, Liu XZ, Han F, Yu H, Longo-Guess C, Yang B, et al. Ush1c gene expression levels in the ear and eye suggest different roles for Ush1c in neurosensory organs in a new Ush1c knockout mouse. Brain Res. 2010;1328: 57–70. pmid:20211154
- 81. Pfaffl MW. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001;29: e45. pmid:11328886
- 82. Lou X, Dong Y, Xie J, Wang X, Yang L, Tokuda M, et al. Comparing the cultivated cochlear cells derived from neonatal and adult mouse. J Trans Med. 2014;12: 150. pmid:24884939
- 83. Legan PK, Lukashkina VA, Goodyear RJ, Kössl M, Russell IJ, Richardson GP. A targeted deletion in α-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback. Neuron. 2000;28: 273–285. pmid:11087000
- 84. Russell IJ, Legan PK, Lukashkina VA, Lukashkin AN, Goodyear RJ, Richardson GP. Sharpened cochlear tuning in a mouse with a genetically modified tectorial membrane. Nat Neurosci. 2007;10: 215–223. pmid:17220887
- 85. Erkman L, McEvilly RJ, Luo L, Ryan AK, Hooshmand F, O’Connell SM, et al. Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development. Nature. 1996;381: 603–606. pmid:8637595
- 86. Qu Y, Tang W, Zhou B, Ahmad S, Chang Q, Li X, et al. Early developmental expression of connexin26 in the cochlea contributes to its dominate functional role in the cochlear gap junctions. Biochem Biophys Res Commun. 2012;417: 245–250. pmid:22142852
- 87. Green GE, Scott DA, McDonald JM, Woodworth GG, Sheffield VC, Smith RJ. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness. JAMA. 1999;281: 2211–2216. pmid:10376574
- 88. Ortolano S, Di Pasquale G, Crispino G, Anselmi F, Mammano F, Chiorini JA. Coordinated control of connexin 26 and connexin 30 at the regulatory and functional level in the inner ear. Proc Natl Acad Sci. 2008;105: 18776–18781. pmid:19047647
- 89. Jagger DJ, Forge A. Connexins and gap junctions in the inner ear–it’s not just about K+ recycling. Cell Tissue Res. 2015;360: 633–644. pmid:25381570
- 90. Zhu Y, Chen J, Liang C, Zong L, Chen J, Jones RO, et al. Connexin26 (GJB2) deficiency reduces active cochlear amplification leading to late-onset hearing loss. Neuroscience. 2015;284: 719–729. pmid:25451287
- 91. Mistrík P, Ashmore J. Using a large scale computational model to study the effect of longitudinal and radial electrical coupling in the cochlea. Concepts and Challenges in the Biophysics of Hearing. 2009. pp. 377–384.
- 92. Mistrík P, Mullaley C, Mammano F, Ashmore J. Three-dimensional current flow in a large-scale model of the cochlea and the mechanism of amplification of sound. J R Soc Interface. 2009;6: 279–291. pmid:18682366
- 93. Mistrík P, Ashmore JF. Reduced electromotility of outer hair cells associated with connexin-related forms of deafness: an in silico study of a cochlear network mechanism. J Assoc Res Otolaryngol. 2010;11: 559–571. pmid:20635191
- 94. Zhou X-X, Chen S, Xie L, Ji Y-Z, Wu X, Wang W-W, et al. Reduced connexin26 in the mature cochlea increases susceptibility to noise-induced hearing loss in mice. Int J Mol Sci. 2016;17: 301. pmid:26927086
- 95. Forge A, Jagger DJ, Kelly JJ, Taylor RR. Connexin30-mediated intercellular communication plays an essential role in epithelial repair in the cochlea. J Cell Sci. 2013;126: 1703–1712. pmid:23424196
- 96. Martínez AD, Acuña R, Figueroa V, Maripillan J, Nicholson B. Gap-junction channels dysfunction in deafness and hearing loss. Antioxid Redox Sign. 2009;11: 309–322. pmid:18837651
- 97. Simmons AM, Boku S, Riquimaroux H, Simmons JA. Auditory brainstem responses of Japanese house bats (Pipistrellus abramus) after exposure to broadband ultrasonic noise. J Acoust Soc Am. 2015;138: 2430–2437. pmid:26520325
- 98. Simmons AM, Hom KN, Warnecke M, Simmons JA. Broadband noise exposure does not affect hearing sensitivity in big brown bats (Eptesicus fuscus). J Exp Biol. 2016;219: 1031–1040. pmid:27030779
- 99. Hom KN, Linnenschmidt M, Simmons JA, Simmons AM. Echolocation behavior in big brown bats is not impaired after intense broadband noise exposures. J Exp Biol. 2016; jeb.143578. pmid:27510961
- 100. Surlykke A, Kalko EKV. Echolocating bats cry out loud to detect their prey. Giurfa M, editor. PLoS ONE. 2008;3: e2036. pmid:18446226
- 101. Kidokoro Y, Karasawa K, Minowa O, Sugitani Y, Noda T, Ikeda K, et al. Deficiency of transcription factor Brn4 disrupts cochlear gap junction plaques in a model of DFN3 non-syndromic deafness. Scemes E, editor. PLoS ONE. 2014;9: e108216. pmid:25259580
- 102. Rubel EW, Fritzsch B. Auditory system development: primary auditory neurons and their targets. Annu Rev Neurosci. 2002;25: 51–101. pmid:12052904
- 103. Kirwan JD, Bekaert M, Commins JM, Davies KTJ, Rossiter SJ, Teeling EC. A phylomedicine approach to understanding the evolution of auditory sensory perception and disease in mammals. Evol App. 2013;6: 412–422. pmid:23745134
- 104. Fettiplace R, Fuchs PA. Mechanisms of hair cell tuning. Annu Rev Physiol. 1999;61: 809–834. pmid:10099711
- 105. Rohmann KN, Fergus DJ, Bass AH. Plasticity in ion channel expression sculpts auditory bandwidth for detecting acoustic signals during reproductive cycles. Curr Biol. 2013;23: 678–683. pmid:23562266
- 106. Rohmann KN, Tripp JA, Genova RM, Bass AH. Manipulation of BK channel expression is sufficient to alter auditory hair cell thresholds in larval zebrafish. J Exp Biol. 2014;217: 2531–2539. pmid:24803460