Little is known about the molecular mechanisms underlying mammalian touch transduction. To identify novel candidate transducers, we examined the molecular and cellular basis of touch in one of the most sensitive tactile organs in the animal kingdom, the star of the star-nosed mole. Our findings demonstrate that the trigeminal ganglia innervating the star are enriched in tactile-sensitive neurons, resulting in a higher proportion of light touch fibers and lower proportion of nociceptors compared to the dorsal root ganglia innervating the rest of the body. We exploit this difference using transcriptome analysis of the star-nosed mole sensory ganglia to identify novel candidate mammalian touch and pain transducers. The most enriched candidates are also expressed in mouse somatosesensory ganglia, suggesting they may mediate transduction in diverse species and are not unique to moles. These findings highlight the utility of examining diverse and specialized species to address fundamental questions in mammalian biology.
Citation: Gerhold KA, Pellegrino M, Tsunozaki M, Morita T, Leitch DB, Tsuruda PR, et al. (2013) The Star-Nosed Mole Reveals Clues to the Molecular Basis of Mammalian Touch. PLoS ONE 8(1): e55001. doi:10.1371/journal.pone.0055001
Editor: Michael N. Nitabach, Yale School of Medicine, United States of America
Received: October 10, 2012; Accepted: December 21, 2012; Published: January 30, 2013
Copyright: © 2013 Gerhold 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.
Funding: The authors are supported by a U.S. National Institutes of Health Innovator Award DOD007123A, the Pew Scholars Program, and the McKnight Scholars Fund (to DMB) and NSF grant 0844743 (to KCC). 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.
Despite the ubiquitous importance of touch for all organisms, understanding the molecular basis of mechanosensory transduction in mammals remains a major challenge. This is due in part to the diversity of touch-sensitive neurons that are specialized to detect a variety of complex mechanical stimuli in the environment and in part to the diffuse localization of primary afferents throughout the body. Although forward genetic screens have identified a number of molecules mediating invertebrate mechanotransduction , we are only now beginning to uncover molecules that mediate the unique functions of touch receptors in mammals. Few mechanically-gated ion channels have been identified, ensembles of proteins may be required for normal mechanoreceptor function, and differences in transduction molecules among fiber subtypes and across species remain unknown.
Here we take a different approach to identifying candidate molecules underlying mammalian touch by exploring one of nature’s experiments in the enrichment and amplification of mechanotransduction molecules, the tactile epidermis of the star-nosed mole. Star-nosed moles (Condylura cristata) are renowned for the unusual mechanosensory appendages that ring their nostrils, collectively called the star (Figure 1A). These 22 tactile “rays” are covered with tens of thousands of domed epidermal touch organs called Eimer’s organs (Figure 1B). The star is only about a centimeter across, yet is innervated by over 100,000 myelinated nerve fibers, giving it the highest innervation density of any mammalian skin surface , . Not surprisingly, the tactile receptive fields on the star are the smallest reported for any mammal, providing unparalleled tactile resolution . These features make star-nosed moles a promising, if unconventional system in which to explore the molecular biology of mammalian mechanotransduction.
(A) Image of a star-nosed mole. (B) EM image of the surface of the star displaying specialized Eimer’s organs. (C) Schematics of an Eimer’s organ in cross-section showing the column of central free nerve endings (CF) and finer peripheral free nerve endings (PF) which surround the central column. The epithelial cell layers are bracketed on the left (red = stratum corneum; orange = epidermis; green = dermis) and other mechanoreceptive complexes found in the Eimer’s organ (MC = Merkel cell, PC = Pacinian corpuscle). (D) Confocal images of star-nosed mole tissue stained for NF200 (green) and substance P (red). In the enlarged box, a cross-section of the star and a single Eimer’s organ. Narrow arrow indicates a substance P-positive fiber, wide arrow indicates NF200-positive fibers, scale bar = 50 µm. (E-F) Epifluorescence images of the TG (E) and DRG (F) stained for peripherin (red) and NF200 (green), with histograms showing the number of cells stained in one field binned by average raw fluorescence units (RFU) per cell. Scale bar = 400 µm, n = 5 sections/tissue.
What are the cellular and molecular building blocks that endow the star with such high tactile sensitivity? To address this question, we characterized the subtypes of somatosensory neurons that innervate the star, identified molecules enriched in these neurons and performed functional cellular and behavioral studies. Our data show that the star organ is innervated by a large number of touch-sensitive neurons in the trigeminal ganglia (TG). The specialization of the star results in a higher number of light touch-sensitive cells in the TG versus the dorsal root ganglia (DRG), and conversely, a higher proportion of nociceptors in the DRG. We exploit this difference to identify novel candidate mammalian molecular force transducers, including cyclic nucleotide gated channels, that mediate touch and pain.
The Star is Innervated by a Plethora of Putative Light Touch Neurons
We first characterized the fiber types that innervate the Eimer’s organs of the star. In mammals, the detection of noxious chemical, mechanical and thermal stimuli is thought to be mediated by unmyelinated C-fibers and lightly myelinated Aδ-fibers, both of which terminate as free nerve endings in the skin. Detection of innocuous tactile stimuli is thought to be mediated by heavily myelinated Aβ-fibers that innervate corpuscles and other specialized structures in the skin, Aδ-fibers that innervate guard hairs, and a small number of C-fibers . Each Eimer’s organ contains two classical light touch receptors, a lamellated corpuscle and a Merkel cell, but is also innervated by a column of free nerve endings that terminate in the superficial epidermis (Figure 1C; ). Surprisingly, and consistent with a role in light touch detection, the majority of these fibers stained heavily for NF200 (Figure 1D), a marker of myelinated putative touch receptors , and myelin basic protein (Figure S1A). Sparse substance P staining, a marker of peptidergic C-fiber nociceptors , was observed in a few smaller fibers at the periphery of the organ (Figure 1D). The low levels of substance P staining are not simply due to poor antibody affinity, as the mole cornea is densely innervated by substance P-positive fibers (Figure S1B). Likewise and similar to other mammals , the glabrous skin of the hindpaw displays robust, non-overlapping substance P and NF200 staining (Figure S1C). These results demonstrate that the star organ is unique in that there is high-density innervation by light touch receptors and that many of the myelinated fibers terminate as free nerve endings in the epidermis.
The Star-nosed Mole has Specialized Trigeminal Ganglia
We next asked whether the dense innervation of the star arises from robust branching of TG neurons or from an enrichment of light touch neurons originating in the TG. Preferential innervation by somatosensory fiber subtypes is observed in other tissues, such as the mouse cornea (Figure S1D), where the dense innervation of nociceptors is achieved by robust branching of projections from a small number of TG neurons (∼1%) in the ophthalmic track . As such, there is no enrichment of nociceptors in the mouse TG (Figure S2), which contain similar numbers of myelinated light touch receptors (49.2±16.5%) and nociceptors (42.6±10.7%).
Unlike mouse sensory ganglia, immunofluoresence analysis of mole sensory ganglia showed a higher percentage of NF200-positive neurons (57.2±9.6%) compared to peripherin-positive neurons (13.4±7.4%) in the TG (Figure 1E). In contrast, the mole DRG displayed similar numbers of NF200- and peripherin-positive cells (36.1±6.2% vs 35.0±6.5%; Figure 1F). As in the mouse, the star-nosed mole NF200-positive neurons possess significantly larger somata than peripherin-positive neurons in both the TG and DRG (TG: 180.4±5.97 µm2 vs 105±6.29 µm2, p = 0.03; DRG: 234±14.1 µm2 vs 150±23.7 µm2, p = 0.04, n = 3, one-way ANOVA), a strong indication that these cells may function in light touch detection. These data reveal a novel anatomical specialization of the mole somatosensory system whereby an enrichment of light touch fibers in the star arises both from branching  and from an increased number of putative light touch neurons in the TG.
The Star-nosed Mole Trigeminal Ganglion Contains More Mechanosensitive Neurons than the Dorsal Root Ganglion
These data predict that the star-nosed mole TG are functionally enriched in cells that detect innocuous mechanical stimuli while the DRG are enriched in capsaicin- and heat-sensitive neurons. Thus, we used calcium imaging to compare the activity of cultured neurons isolated from the mole TG and DRG (Figure 2A). We subjected neurons to capsaicin, mustard oil and menthol (Figure 2B, left), irritants that preferentially activate nociceptors via TRPV1, TRPA1 and TRPM8, respectively –, and examined responses to hydroxy-alpha-sanshool (sanshool), hypo-osmotic stimuli, and low-magnitude radial stretch (10%, Figure 2B, right), which predominantly activate light touch neurons . Consistent with the antibody staining, capsaicin, mustard oil, and menthol activated a significantly higher percentage of neurons in the DRG compared to the TG (DRG: 36.1±8.2% versus TG: 14.7±2.8% for capsaicin). Conversely, hypotonic solution, sanshool and radial stretch activated a significantly higher percentage of TG neurons than DRG neurons (TG: 79.6±5.9% versus DRG: 33.86±2.9% for stretch). These results demonstrate that the star-nosed mole TG are highly specialized anatomically and functionally to mediate high tactile sensitivity.
(A) Representative images of Fura-2 loaded star-nosed mole TG and DRG neurons before and after exposure to 10% radial stretch and capsaicin (1 µM). (B) Average percentage of TG (green) and DRG (grey) neurons activated by capsaicin (Cap), mustard oil (MO), menthol (Me), hydroxy-α-sanshool (San), hypotonic solution (Hypo) and 10% radial stretch (Str) (error bars represent s.e.m. n = 4 samples, **p< 0.01, *p< 0.05 by one way ANOVA).
Using Transcriptome Profiling to Identify Candidate Touch Transducers
The enrichment of functional light touch neurons in the TG and nociceptors in the DRG suggests that these tissues vary at a molecular level. If this is indeed the case, comparing transcripts may lead to the identification of molecular players that mediate touch or pain transduction. We used mRNA-Seq to detect transcripts expressed in mole TG and DRG, and we compared expression levels between these two tissues. Currently there is no available annotated genome for the star-nosed mole, or any other member of the order Soricomorpha. As such, we mapped mRNA-Seq reads to multiple known mammalian transcriptomes iteratively. Using the Stampy algorithm , reads from TG and DRG were first aligned to the Homo sapiens transcriptome; unmapped reads were then aligned to the Canis lupus familiaris transcriptome, and finally to the Mus musculus transcriptome. This strategy successfully aligned 42%–65% of sequenced reads per sample. This is quite high, given that reads typically align at ∼87% to a well annotated genome . The DESeq package  was employed to test for differential gene expression between the TG and DRG samples (padj < 0.05). We identified 3231 genes with significantly elevated expression in the TG and 3033 in the DRG (Figure 3A). We hypothesized that a number of these genes also differ between mouse TG and DRG, due to the different organ structures, localization, target organ innervation patterns, central and peripheral circuitry and support cells of these ganglia. We carried out a parallel transcriptional profiling analysis of TG and DRG in the mouse and found 51 genes that show significantly higher expression in both the mouse and mole TG compared to DRG and 72 genes more highly expressed in both mouse and mole DRG. For example, Hoxd1 is required for normal nociceptor innervation of thoracic and cervical spinal cord levels , and shows significantly higher expression in both mole and mouse DRG (fold change in DRG vs TG: star-nosed mole = 4.76, padj = 9.26*10−5, mouse = 1.5, padj = 0.034).
(A) Dot plot of expression levels of mapped genes in the star-nosed mole TG and DRG. Genes differentially expressed between TG or DRG (padj< = 0.05) are shown in green and dark grey, respectively. (B) Gene Ontology classification of transmembrane proteins differentially expressed between the star-nosed mole TG and DRG. (C) Dot plot of expression levels of known ion channels in the star-nosed mole TG versus DRG. Genes differentially expressed between TG or DRG (padj< = 0.05) are shown in green and dark grey, respectively. Black dots represent individual genes as labeled. (D) Top channels and channel regulators enriched in mole TG and DRG. This list excludes channels also differentially expressed between mouse ganglia. Table shows gene name in mouse, fold enrichment in mole, and putative ion conductance.
To identify transduction molecules, we limited our analyses to predicted membrane proteins that were not differentially expressed between mouse TG and DRG, and were more highly expressed in mole TG (788 genes) or DRG (1159 genes). The genes belong to a wide variety of classes as verified by Gene Ontology analysis (Figure 3B). Consistent with a higher percentage of large diameter myelinated neurons, the SNM TG showed increased transcript numbers for a larger number of myelin specific transmembrane proteins compared to DRG. Conversely, DRG showed higher expression of a larger number of proteins involved in vesicle trafficking and exocytosis, consistent with an increased number of peptide releasing nociceptors.
In mechanosensory cells, ion channels underlie the transduction of mechanical stimuli into electrical signals. We therefore focused on genes that encode ion channels or channel modulators and are significantly enriched in the DRG or TG (Figure 3C–D). The DRG-enriched genes include a number of channels implicated in nociception including: the tetrodotoxin-insensitive sodium channels Nav1.8 (Scn10a) and Nav1.9 (Scn11a; , ), the cold-sensitive ion channel Trpm8 , the heat-sensitive channel Trpm3 , the irritant receptor Trpa1 , , the heat- and capsaicin-receptor Trpv1  and the putative mechanosensitive channel Piezo2 (Fam38b; , ).
Several ion channels previously implicated in mechanotransduction were enriched in the TG, including: ASIC3 (Accn3), a homologue of the MEC4/10 channels which transduce mechanosensitive currents in Caenorhabditis elegans , Piezo1 (Fam38a), a mechanosensitive channel expressed in mouse kidney, lung and skin , Cnga2, a cyclic-nucleotide-gated channel required for mechanical- and odorant-evoked responses in olfactory neurons , and Cnga3 which plays a role in inflammatory hypersensitivity to thermal and mechanical stimuli . In addition, we observed significantly higher expression in the TG of Stoml3 and Stom, homologues of the Caenorhabditis elegans mec-2 gene that modulates mechanosensitive channels ; both of these proteins have also been implicated in light touch detection in mammals . These data show that by comparing the star-nosed mole DRG and TG transcriptome we can classify channels and signaling molecules as either pain, or light touch candidate transducers.
To validate our high-throughput expression analysis, we performed quantitative PCR (qPCR) on several of the signaling molecules enriched in the TG and DRG (Figure 4A). As expected, qPCR of Fam38a, Cnga2 and Stoml3 showed higher expression in the TG, while Trpa1 and Trpv1 were more highly expressed in the DRG, though differences in Fam38a expression were not significant. We also analyzed expression of CNGA2 protein in mole sensory ganglia and the star. Consistent with a role in light touch detection, and our transcriptome profiling, immunofluorescence analysis of mole sensory ganglia stained with antibodies against CNGA2 showed a higher percentage of CNGA2-positive neurons in the TG as compared to the mole DRG (Figure 4 B–D); these cells also displayed robust NF200 immunoreactivity. To determine if Cnga2 is expressed in mole TG neurons that project to the star, we examined Cnga2 staining in the fibers that innervate the star. Indeed, Eimer’s organs are densely innervated by CNGA2-positive fibers, the vast majority (>90%) of which are also NF200-positive (Figure 4E–F). These data show that our transcriptome expression analysis can indeed identify novel candidate transducers that are enriched in light touch neurons of the star-nosed mole.
(A) qPCR analysis of selected transcripts in TG (green) and DRG (grey). Results show average expression normalized to Gapdh (n = 3 samples/tissue). (B-F) Images of star-nosed mole tissue stained with antibody against CNGA2 (green) and NF200 (red). (B) Trigeminal ganglia (TG) show stronger staining for CNGA2 than (C) dorsal root ganglia (DRG). (D) Percentage of total neurons stained positive for CNGA2 in TG (green) and DRG (grey) n = 4 sections/tissue. (E) Cross section of a single Eimer’s organ and (F) nerve tracts innervating multiple Eimer’s organs show strong CNGA2 staining and high overlap with NF200 staining. Error bars represent s.e.m. **p< 0.01, *p< 0.05, NS = p>0.05 by one way ANOVA).
Candidate Touch Transducers in the Mouse Somatosensory System
Definitive evidence for the involvement of a gene in mechanotransduction must come from functional assays. Unfortunately, such assays are not possible in star-nosed moles. We thus examined expression of the most TG- and DRG-enriched channels in mouse sensory ganglia. ∼85% of these channels were detected in mouse TG and DRG by RT-PCR (Figure 5A). Many of these channels have not been previously implicated in mammalian somatosensory transduction. qPCR of mouse ganglia also demonstrated expression of the TG-enriched ion channels Cnga2, Cnga3, Cnga4, and Fam38a, as well as the DRG-enriched TRPA1 and TRPV1 (Figure 5B). Overall, these channels represent excellent candidates to probe in the more tractable mouse model.
(A) Ion channels enriched in mole TG and DRG that were amplified by RT-PCR from mouse TG and DRG. All genes were amplified independently from TG and DRG samples isolated from two mice. Channels shown in bold are candidates that have not been previously reported as expressed in somatosensory neurons. (B) qPCR analysis of selected genes in mouse TG and kidney. Results show average expression normalized to Gapdh (n = 3). Error bars represent s.e.m.
Despite intensive study in recent years, the molecular basis of mechanotransduction remains poorly understood and few mechanically gated ion channels have been identified. Here we take a new approach by investigating the hypertrophied mechanosensory epidermis of the star-nosed mole. We showed that the dense innervation of the star by myelinated light touch fibers originates from a specialized trigeminal system. In general, the mammalian somatosensory system is broadly tuned to detect a diverse array of innocuous and noxious stimuli. Unlike other mammalian somatosensory ganglia, or even the star-nosed mole DRG that innervate the body, the star-nosed mole TG contain relatively few classical nociceptors (Figure 1E–F, 2B). Thus, the high tactile acuity of the star may arise at the expense of thermal and chemical sensitivity, as the lack of peptidergic C-fibers and nociceptive molecules (e.g. TRPA1 and TRPV1) may affect the ability of the star to detect irritants and other noxious stimuli. Consistent with this, topical application of capsaicin to the hindpaw elicits nocifensive responses similar to those reported in rodents, but application to the star evokes no obvious behaviors (n = 3 animals).
The star-nosed mole has adapted a new strategy for achieving high tactile acuity, namely a cellular and molecular specialization of the trigeminal ganglia that innervate the star. We exploited this specialization to identify molecules enriched in the DRG and TG. Transcript analysis offers an unbiased approach to identify genes of interest, but is usually restricted to organisms for which genome information is widely available. Since there is no annotated genome data for the star-nosed mole, or any close relative, we used iterative mapping to assign the identity of reads. The use of this approach to identify novel players in touch and pain is validated by the differential expression of molecules already known to play keys roles in pain transduction in the DRG, and genes implicated in innocuous touch transduction in the TG. For example, TRPV1 in nociceptors and Stoml3 in touch neurons.
RNASeq analysis revealed an enrichment of nociceptive transcripts in the mole DRG versus the TG. For example, TRPV1 expression is ∼10-fold higher in the mole DRG than the TG and Cnga2 levels are ∼20-fold higher in the mole TG versus DRG (Figure 3D). Some of this enrichment can be accounted for by the varying numbers of neuronal subtypes in the DRG and TG as measured by functional imaging and histology. However, while we see 10–20 fold differences in transcript levels between the DRG and TG, the number of TRPV1- or Cnga2-positive cells only varies by ∼3-fold (Figure 2B, 4D). These findings suggest that expression differences between ganglia may arise from both a shift in the number of nociceptors, as well as expression differences within any given neuronal subtype.
We identified a number of novel candidate genes enriched in mole TG that may mediate mammalian somatosensory mechanotransduction. Cnga2 and Cnga4, the most highly enriched channels in the mole TG, play an important role in signal transduction in both the visual and olfactory systems . Cnga2 is proposed to mediate both chemosensory and mechanosensory responses evoked by breathing in the mouse olfactory system . If CNG channels play a role in somatosensory transduction, other components of the cyclic nucleotide pathway should be expressed in sensory neurons. This is indeed the case, as mouse sensory ganglia also express two additional genes required for cAMP signaling and olfactory transduction and behaviors in mice, the G protein (Gnal) and adenylate cyclase 3 (Adcy3) (data not shown; , ). These data suggest that cyclic nucleotide signaling may represent a new signaling pathway in touch transduction. More broadly, these findings suggest that transduction mechanisms may be conserved between divergent sensory systems. Indeed, transcriptional analysis of the Droshophila Johnston’s organ recently identified a number of chemo- and photo-transduction molecules that also play a role in auditory transduction .
Fam38a (Piezo1) is an ion channel that induces mechanically-evoked responses in many different cell types. Previous studies showed high expression in mouse kidney, lung and skin, but relatively low expression in sensory ganglia. Our RNASeq and qPCR data shows expression in mole TG and DRG. This led us to re-examine expression of Fam38a in mouse sensory ganglia. Surprisingly, we amplified Fam38a from both mouse TG and DRG and observed comparable levels of expression in mouse TG and kidney (Figure 5B). Likewise, RNASeq of mouse ganglia also shows expression of Fam38a, suggesting that this protein may play a role in mediating light touch transduction in mice.
Finally, we identified a number of novel, uncharacterized genes enriched in TG and DRG that contain one or more transmembrane domains and that were not previously classified as organellar. These genes, along with CNG channels and Piezo1, may participate in different aspects of transduction, acting as detectors, modulators and/or amplifiers of mechanical stimuli. Each subtype of light touch receptor has distinct mechanical thresholds, sensory adaptation properties and action potential waveforms, and it is predicted that such diversity is driven by a unique repertoire of force transducers. Thus, future studies will determine if these genes are expressed in distinct subsets of somatosensory neurons, and what role they play in detecting diverse somatosensory stimuli in vivo.
Our results emphasize the utility of examining both traditional model organisms and less common species that may provide important clues to sensory system function. August Krogh articulated the principle that “for such a large number of problems there will be some animal of choice, or a few such animals, on which it can be most conveniently studied” . In the spirit of this approach, we exploited the high tactile acuity of the star-nosed mole to identify a multitude of candidate molecules that may mediate innocuous and noxious somatosensory stimuli. The function of these molecules can now be probed in more traditional model organisms.
Materials and Methods
Star-nosed moles were collected in Potter County, Pennsylvania, under permit COL00087. Wild type adult female mice C57/Bl6 (Jackson Labs) were used for sectioning, RT-PCR and qPCR. All procedures followed guidelines for the care and use of laboratory animals from the National Institutes of Health and were approved by the Vanderbilt University Institutional Animal Care and Use Committee and the UC Berkeley Animal Care and Use Committee.
Five star-nosed moles and two mice were anesthetized with 250 mg/kg i.p. injection of sodium pentobarbital and perfused with 1X PBS (pH 7.3) followed by 4% paraformaldehyde (PFA) in PBS. Trigeminal ganglia, dorsal root ganglia, star tissue, hindpaw skin and cornea were collected. Tissue was post-fixed for >4 hours in 4% PFA and incubated overnight in 20% sucrose at 4°C. Trigeminal ganglia, dorsal root ganglia, hindpaw skin and star were embedded in Tissue-Tek optimal, sectioned at 10 or 15 µm, and mounted onto glass coverslips for staining.
Sections were blocked for 90 minutes in PBST supplemented with 10% normal goat serum and incubated overnight at 4°C with primary antibody. Primary antibodies were diluted as follows: mouse anti-NF200 (Sigma) and rabbit anti-peripherin 1∶1000 (Millipore), guinea pig anti-substance P 1∶700, rabbit anti-S100 1:300 (ThermoFisher), rabbit anti-CNGA2 1:500 (Alomone labs). Sections were washed and incubated for one hour at room temperature in 1∶1000 secondary antibody. Secondary antibodies (Invitrogen) were used as follows: anti-mouse Alexa 488 or 568 for NF200, anti-rabbit Alexa 568 for peripherin, anti-guinea pig Alexa 568 for substance P, Alexa 488 anti-rabbit for S100, and Alexa 488 anti-rabbit for CNGA2. Intact corneas were stained directly after sucrose incubation.
Fluorescence images were captured using an inverted fluorescence microscope (IX71, Olympus), illuminated with a xenon light source (Lambda LS-xl, Sutter) with a FITC excitation and emission set for Alexa 488 (Chroma) and Texas Red excitation and emission set for Alexa 568 (Chroma). Images were captured using MetaMorph (Molecular Devices). Confocal images were collected using Leica TCS SL confocal microscope. Summation projections were compiled from a series of 8 images (1 µM Z-steps, MetaMorph).
For determining percentages of positive cells, cell boundaries were determined by hand using bright field images and the average intensity of each region was calculated (MetaExpress). Cells were defined as being positive for a specific marker if their intensity was more than 30% above background.
DRG and TG cells were cultured as previously described . Briefly, star-nosed moles were euthanized and dorsal root ganglia and trigeminal ganglia were dissected. Ganglia were digested for 20 minutes in 7 mg/mL collagenase P (Roche) then for 2 minutes in 0.25% trypsin. Cells were dissociated manually by trituration and plated on glass coverslides coated with 1 mg/mL Poly-D-Lysine and 0.1 mg/mL laminin. Cells were cultured overnight at 37°C before imaging.
Calcium imaging was performed as previously described for mouse neurons . Cells were loaded for an hour at room temperature with Fura-2AM (10 µM, Invitrogen) in Ringer’s solution (140 mM NaCl, 5 mM KCl, 2 mM CaCl2, 1 mM MgCl2, 10 mM D-glucose, 10 mM HEPES) supplemented with 0.2% pluronic acid (Invitrogen). Ratiometric calcium imaging was performed using alternating 340 nm and 380 nm excitation filters with images collected every three seconds. Responsive cells were defined as those whose calcium concentration increased more than 10% above the baseline after application of the stimulus.
Star nosed mole or mouse tissues were removed and homogenized in Trizol (Invitrogen). Total RNA was extracted as per the manufacturer’s instructions. Total RNA was either DNAsed, re-purified (RNAeasy, Quiagen) and reverse transcribed (SuperScriptIII, Invitrogen) for qPCR or RT-PCR, or further purified with two rounds of poly-A selection (Dynabeads mRNA purification Kit, Invitrogen) for sequencing.
Poly-A selected mRNA from trigeminal ganglia and dorsal root ganglia were fragmented using Fragmentation Reagents (Applied Biosystems). Libraries were further prepared using the Genomic Sample Prep Kit following a modified RNA-seq protocol  or the TruSeq kit (Illumina). One to three lanes of each tissue’s library were sequenced on a Genome Analyzer II or HighSeq 200 using the 76, 50 or 36 bp single-end sequencing protocol at the Vincent J. Coates Genomics Sequencing Laboratory at UC Berkeley.
Three (mole) or two (mouse) TG and DRG were used. All samples were derived from single individuals, except one mole DRG, combined from two individuals. Mole reads were mapped as described in the text. Mouse reads were aligned to Mus musculus mRNA sequences. Homo sapiens database: Nov 25th 2010, genome.ucsc.edu. Canis lupus familiaris and Mus musculus: Nov28th 2010, ncbi.nlm.nih.gov. Alignments were performed using Stampy v1.0.11  with a substitution rate = 0.03. The read count for a given gene was the sum of reads aligning to the transcript(s) assigned to an entry in the Entrez Gene database (ncbi.nlm.nih.gov, Jan 2011). For mole genes, read count was the sum of all reads aligning to the homologs of that gene in the three organisms. Homology was based on the HomoloGene database (build 64) and manual annotation. Differential expression was assessed using the DESeq package for R  which corrected for multiple comparisons (padj).
Transmembrane Domain Prediction
Transmembrane domains were identified by removing signal peptides predicted with SignalP3.0 , and by analyzing the remaining sequence with SOSUI , TMHMM2.0 , and TMpred  programs. A protein was considered having a transmembrane domain if at least two of the three programs predicted at least one transmembrane region.
RNA was extracted from 3 moles as described above. qPCR was performed using SYBR GreenER (Invitrogen) on a StepOnePlus™ Real-Time PCR system (Applied Biosystems). qPCR reactions were run in 10 µL using 1 µL of product from the RT reaction with the primers listed below. CT values were calculated as the average of 2 wells. Fold expression for each was calculated averaging normalized CT values from two runs, assuming 100% efficiency. Final values were calculated as an average of the biological replicates for each tissue type.
Fam38a: Fwd TCTTCCTCTTCCAGGGGTTC, Rev ACCAGGGACATGAAGAGCAG
Cnga2: Fwd CTGGAGACCAAGATGAAGCAGA, Rev ATTACGAAGACGGAGCCCTACA
Stoml3: Fwd GAGTCACCCATAGCCCTCCA, Rev GACCACCCATGCCCTCTAGT
Trpv1: Fwd TGAAGACCTTGTTTGTGGACAG, Rev CGGGTGTAGTAGAGCATGTTGG
Trpa1: Fwd CTTATTGGTTTGGCAGTTGGTG, Rev CGGTTGGGGTAGACAGTGATG
Gapdh: Fwd CACGGCCACCCAGAAGAC, Rev TCAGATCCACGACGGACAC.
Trigeminal ganglia, dorsal root ganglia or a mix of tissues (liver, heart, lungs, kidneys, pancreas and brain) were extracted and cDNA was produced as described above with or without reverse transcriptase (no RT control). PCR was performed on 1 µL of product using Phusion Taq polymerase (NEB) and the primers described in Table S1.
Star-nosed mole NF200-positive fibers display similar characteristics to those described in mouse. (A) All NF200-positive fibers (green) are myelin basic protein-positive (red). Epifluorescence image of a section through a bundle of fibers projecting through the nose. (B) Mole cornea shows strong substance P staining. Confocal image of the mole cornea with substance P (red) and NF200 (green), scale bar = 20 µm. (C) Mole hindpaw shows robust staining of both substance P (red) and NF200 (green). Confocal image, scale bar = 50 µm. (D) Mouse cornea shows similar staining to mole cornea. Confocal image, scale bar = 20 µm.
Mouse TG and DRG show similar staining for peripherin and NF200. Peripherin (red) and NF200 (green) staining of the TG (A) and DRG (B). (C) Quantification of the percent of NF200 and peripherin positive cells in these tissues (NS = p>0.1; n = 3 sections, error bars represent s.e.m.).
Primers for amplification of star-nosed mole enriched genes in mouse.
We thank Dr. Allan Basbaum for generously providing the substance P antibody and Dr. John Ngai and members of our laboratories for helpful discussions.
Conceived and designed the experiments: KAG MP DMB. Performed the experiments: KAG MP MT TM DMB. Analyzed the data: KAG MP MT TM DMB. Contributed reagents/materials/analysis tools: KAG MP DBL PRT RBB KCC DMB. Wrote the paper: KAG MP KCC DMB.
- 1. Lumpkin EA, Marshall KL, Nelson AM (2010) The cell biology of touch. J Cell Biol 191: 237–248.
- 2. Catania KC (1995) Structure and innervation of the sensory organs on the snout of the star-nosed mole. J Comp Neurol 351: 536–548.
- 3. Catania KC (1996) Ultrastructure of the Eimer’s organ of the star-nosed mole. J Comp Neurol 365: 343–354.
- 4. Catania KC, Remple FE (2005) Asymptotic prey profitability drives star-nosed moles to the foraging speed limit. Nature 433: 519–522.
- 5. Lumpkin EA, Caterina MJ (2007) Mechanisms of sensory transduction in the skin. Nature 445: 858–865.
- 6. Lawson SN, Waddell PJ (1991) Soma neurofilament immunoreactivity is related to cell size and fibre conduction velocity in rat primary sensory neurons. J Physiol 435: 41–63.
- 7. Lawson SN, Crepps BA, Perl ER (1997) Relationship of substance P to afferent characteristics of dorsal root ganglion neurones in guinea-pig. J Physiol 505 ( Pt 1): 177–191.
- 8. Zylka MJ, Rice FL, Anderson DJ (2005) Topographically distinct epidermal nociceptive circuits revealed by axonal tracers targeted to Mrgprd. Neuron 45: 17–25.
- 9. Marfurt CF, Kingsley RE, Echtenkamp SE (1989) Sensory and sympathetic innervation of the mammalian cornea. A retrograde tracing study. Invest Ophthalmol Vis Sci 30: 461–472.
- 10. Bautista DM, Siemens J, Glazer JM, Tsuruda PR, Basbaum AI, et al. (2007) The menthol receptor TRPM8 is the principal detector of environmental cold. Nature 448: 204–208.
- 11. Jordt SE, Bautista DM, Chuang HH, McKemy DD, Zygmunt PM, et al. (2004) Mustard oils and cannabinoids excite sensory nerve fibres through the TRP channel ANKTM1. Nature 427: 260–265.
- 12. Tominaga M, Caterina MJ, Malmberg AB, Rosen TA, Gilbert H, et al. (1998) The cloned capsaicin receptor integrates multiple pain-producing stimuli. Neuron 21: 531–543.
- 13. Bhattacharya MR, Bautista DM, Wu K, Haeberle H, Lumpkin EA, et al. (2008) Radial stretch reveals distinct populations of mechanosensitive mammalian somatosensory neurons. Proc Natl Acad Sci U S A 105: 20015–20020.
- 14. Lunter G, Goodson M (2010) Stampy: A statistical algorithm for sensitive and fast mapping of Illumina sequence reads. Genome Res 21: 936–939.
- 15. Li H, Durbin R (2009) Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 25: 1754–1760.
- 16. Anders S, Huber W (2010) Differential expression analysis for sequence count data. Genome Biol 11: R106.
- 17. Guo T, Mandai K, Condie BG, Wickramasinghe SR, Capecchi MR, et al. (2011) An evolving NGF-Hoxd1 signaling pathway mediates development of divergent neural circuits in vertebrates. Nat Neurosci 14: 31–36.
- 18. Abrahamsen B, Zhao J, Asante CO, Cendan CM, Marsh S, et al. (2008) The cell and molecular basis of mechanical, cold, and inflammatory pain. Science 321: 702–705.
- 19. Djouhri L, Fang X, Okuse K, Wood JN, Berry CM, et al. (2003) The TTX-resistant sodium channel Nav1.8 (SNS/PN3): expression and correlation with membrane properties in rat nociceptive primary afferent neurons. J Physiol 550: 739–752.
- 20. Vriens J, Owsianik G, Hofmann T, Philipp SE, Stab J, et al. (2011) TRPM3 is a nociceptor channel involved in the detection of noxious heat. Neuron 70: 482–494.
- 21. Kwan KY, Allchorne AJ, Vollrath MA, Christensen AP, Zhang DS, et al. (2006) TRPA1 contributes to cold, mechanical, and chemical nociception but is not essential for hair-cell transduction. Neuron 50: 277–289.
- 22. Caterina MJ, Leffler A, Malmberg AB, Martin WJ, Trafton J, et al. (2000) Impaired nociception and pain sensation in mice lacking the capsaicin receptor. Science 288: 306–313.
- 23. Coste B, Mathur J, Schmidt M, Earley TJ, Ranade S, et al. (2010) Piezo1 and Piezo2 are essential components of distinct mechanically activated cation channels. Science 330: 55–60.
- 24. Kim SE, Coste B, Chadha A, Cook B, Patapoutian A (2012) The role of Drosophila Piezo in mechanical nociception. Nature 483: 209–212.
- 25. O’Hagan R, Chalfie M, Goodman MB (2005) The MEC-4 DEG/ENaC channel of Caenorhabditis elegans touch receptor neurons transduces mechanical signals. Nat Neurosci 8: 43–50.
- 26. Grosmaitre X, Santarelli LC, Tan J, Luo M, Ma M (2007) Dual functions of mammalian olfactory sensory neurons as odor detectors and mechanical sensors. Nat Neurosci 10: 348–354.
- 27. Heine S, Michalakis S, Kallenborn-Gerhardt W, Lu R, Lim HY, et al. (2011) CNGA3: a target of spinal nitric oxide/cGMP signaling and modulator of inflammatory pain hypersensitivity. J Neurosci 31: 11184–11192.
- 28. Goodman MB, Ernstrom GG, Chelur DS, O’Hagan R, Yao CA, et al. (2002) MEC-2 regulates C. elegans DEG/ENaC channels needed for mechanosensation. Nature 415: 1039–1042.
- 29. Martinez-Salgado C, Benckendorff AG, Chiang LY, Wang R, Milenkovic N, et al. (2007) Stomatin and sensory neuron mechanotransduction. J Neurophysiol 98: 3802–3808.
- 30. Biel M (2009) Cyclic nucleotide-regulated cation channels. J Biol Chem 284: 9017–9021.
- 31. Belluscio L, Gold GH, Nemes A, Axel R (1998) Mice deficient in G(olf) are anosmic. Neuron 20: 69–81.
- 32. Wong ST, Trinh K, Hacker B, Chan GC, Lowe G, et al. (2000) Disruption of the type III adenylyl cyclase gene leads to peripheral and behavioral anosmia in transgenic mice. Neuron 27: 487–497.
- 33. Senthilan PR, Piepenbrock D, Ovezmyradov G, Nadrowski B, Bechstedt S, et al. (2012) Drosophila auditory organ genes and genetic hearing defects. Cell 150: 1042–1054.
- 34. Krogh A (1929) The Progress of Physiology. Science 70: 200–204.
- 35. Marioni JC, Mason CE, Mane SM, Stephens M, Gilad Y (2008) RNA-seq: an assessment of technical reproducibility and comparison with gene expression arrays. Genome Res 18: 1509–1517.
- 36. Bendtsen JD, Nielsen H, von Heijne G, Brunak S (2004) Improved prediction of signal peptides: SignalP 3.0. J Mol Biol 340: 783–795.
- 37. Hirokawa T, Boon-Chieng S, Mitaku S (1998) SOSUI: classification and secondary structure prediction system for membrane proteins. Bioinformatics 14: 378–379.
- 38. Krogh A, Larsson B, von Heijne G, Sonnhammer EL (2001) Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes. J Mol Biol 305: 567–580.
- 39. Hofmann K, Stoffel W (1993) TMbase - A database of membrane spanning proteins segments. Biol Chem Hoppe-Seyler 347: 166.