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Gene loss in keratinization programs accompanies adaptation of cetacean skin to aquatic lifestyle

Experimental Dermatology2015Vol. 24(8), pp. 572–573

Citations Over TimeTop 14% of 2015 papers

Ji Won Oh, Oksung Chung, Yun Sung Cho, Grant R. MacGregor, Maksim V. Plikus

Abstract

The transition to a fully aquatic lifestyle in cetaceans, baleen and toothed whales, was accompanied by sweeping changes in their body plan, anatomy and physiology. Detailed fossil records of ancestral forms between land-dwelling mammals and modern-day cetaceans enshrine whales in biology textbooks as an example of macroevolution 1. The advent of mainstream sequencing technologies has allowed the whole genomes of several cetacean species to be assembled and provisionally annotated. This exciting advance enables studying the genetic basis of mammalian adaptation to life in water, including changes to skin. Genomewide profiles of adaptive mutations in cetaceans can facilitate identification of the genetic causes of rare inherited disorders in humans with whale-like skin manifestations: loss of epidermal barrier function and loss of appendages. Cetacean integument is uniquely suited for an aquatic lifestyle. Their epidermis is smooth and rubber-like on the outside. On the inside, it is exceedingly thick and forms deep, root-like projections into the underlying dermis. This anatomy produces a dramatically increased basal-to-outer surface ratio and results in an expanded basal progenitor compartment, enabling a high epidermal turnover rate. Cetacean skin also has a simplified repertoire of cutaneous appendages: pelage hairs, sweat glands and claws are absent, but few sensory vibrissae form. Interestingly, while in baleen whales vibrissa follicles cycle throughout life, in the majority of dolphins at birth they convert into small, highly innervated sensory pits 2. The general ability of cetaceans to form vibrissae suggests that their lack of body hair is likely caused by the suppression of hair patterning rather than a defect in the hair follicle morphogenesis program per se. Preservation of the follicle-forming program in dolphins for the sake of developing sensory pits highlights the overall importance of the tactile perception of skin appendages, a feature that also co-evolved in birds in form of filoplumes, sensory vibrissa-like feathers 3. Despite its thickness, cetacean epidermis is highly susceptible to dehydration. Indeed, the news commonly covers dramatic rescue attempts of dolphins and whales at high risk of dying once stranded on the beach, with need to be kept constantly wet. A recent study by Strasser et al. 4 lends new insight into the genetic basis of what appears to be an epidermal barrier defect in cetaceans. In most land mammals, the epidermis acquires its barrier function through a terminal differentiation program that includes: (i) aggregation of keratin filaments into bundles, (ii) assembly of the cornified envelope and (iii) sealing of the intercellular spaces with lipids 5. Keratin filament bundling in mammalian epidermis is coordinated by filaggrin, an abundant intermediate-filament binding protein. Genetically, the filaggrin precursor is encoded as part of the larger epidermal differentiation complex (EDC), a prominent gene cluster which includes: (a) multiple calcium-binding S100A proteins; (b) cornified envelope precursors, such as involucrin and loricrin; and (c) other intermediate-filament binding proteins, also known as S100 fused-type proteins (SFTPs) 6. However, in cetaceans things appear somewhat different. By comparing the genomes of five different cetacean species, Strasser et al. 4 made the striking observation that all SFTP genes, with the notable exception of filaggrin, become pseudogenized via introduction of premature stop codons, frameshifts, gaps in exonic sequences or a combination of sequence alterations. In many instances, SFTP homologs were not detected via sequence homology, suggesting these genes were deleted during evolution, or perhaps remain hidden in gaps in the current genome assembly. The latter possibility is a common challenge faced during assembly of highly repetitive genomic regions such as the EDC or HOX gene clusters 7. The assembled sequence size of the EDC is significantly larger in humans and cows, whose genome assemblies are more complete, as compared to cetaceans and pigs, whose genomes are assembled only provisionally and contain a large number of ambiguous bases (Fig. 1). While filaggrin was shown to be present, and tentatively functional, in bottlenose dolphins, killer whales and Chinese river dolphins, it was not detected (either due to being deleted in vivo, or not yet mapped in silico) in sperm whales and minke whales. Phylogenetically, sperm whales belong to the suborder of toothed whales (Odontoceti) together with dolphins, while the minke whale is a baleen whale (suborder of Mysticeti). Thus, filaggrin loss in sperm and minke whales would presumably require two independent evolutionary events, one in baleen whales and another in the subset of toothed whales. Studies in mice and humans indicate that pseudogenization of SFTPs can contribute to the disruption of the epidermal barrier. Prominently, a loss-of-function mutation in filaggrin in ‘flaky tail’ mice disrupts their epidermal barrier and enhances transepidermal antigen transfer 8. Similarly, filaggrin mutations in humans strongly predispose for the development of atopic dermatitis, which results from the increased transcutaneous antigen penetration and subsequent immune reaction 9. Loss of other SFTPs, such as filaggrin 2, was also shown to contribute to epidermal barrier disruption 10. Future studies comparing sequences of other EDC genes, especially components of the cornified envelope, are likely to provide additional insight into the loss of epidermal barrier function in cetaceans. Consistent with the findings of Strasser et al. 4, two recent studies reveal high levels of gene deletion and pseudogenization in other gene clusters involved in keratinization, α-keratin and keratin-associated protein (KRTAP) clusters. This suggests evolutionary relaxation of selection (i.e. disabling mutations are allowed to accumulate) as a general mechanism driving adaptation of mammalian integument to an extreme ecological niche change 11, 12 (see Data S1). In the future, cetacean pseudogene maps can be referenced to facilitate identification of the genetic causes of orphan human diseases manifested by defects in epidermis, sweat glands and hair follicles. Generally, emerging molecular data support the notion that loss of functional significance, that is, that of epidermal barrier function and fur coat in cetaceans, was accompanied by relaxation in evolutionary selection in related terminal differentiation pathways. Importantly, analogous genetic changes occurred during evolution of human skin – compared to chimpanzees, humans have a premature stop codon in the hair keratin gene KRT41P 13, a mutation that likely coincided with a decreased importance for body hair coverage in hominids. Does the dramatic loss of genes encoding keratinization proteins indicate a general trend for anatomical simplification of ectodermal structures? Not always. Palatal epithelium in baleen whales has evolved into a highly specialized keratinized derivative structure, the baleen, which acts as a massive filter. Baleen is organized into racks of parallel plates. Tongue movements abrade the lingual surface of baleen plates to expose individual hair-like keratinous tubules, which act as sifting units 14. Intriguingly, tensile properties of baleen tubules were shown to be substantial, albeit lower than that of hair. Moreover, baleen in some whales, such as the sei whale, was shown to be highly mineralized (close to 14%), and mineralization significantly contributes to its tensile properties (around 40%) 15. Taken together, the studies by Strasser et al. 4 and others 11, 12 identify cetacean skin as an attractive novel model system for examining the effects of gene loss on skin formation and function. Recent advances in induced-pluripotent stem cell (iPSC) technologies 16 may soon enable working with dolphin and whale iPSC-derived skin cells in the laboratory settings using organotypic culture assay for studying epidermal differentiation and barrier function, or ‘patch’ assay for studying hair formation and hair loss. MVP is supported by the NIH National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) grant R01-AR067273 and Edward Mallinckrodt Jr. Foundation grant. The authors are also thankful to Tsai-Ching Hsi for critical reading of the manuscript. JWO and MVP wrote the paper, OC, YSC and GRM critically revised the paper. The authors have declared no conflicting interests. Data S1. Supplementary Text Figure S1. Vibrissa hairs of Cetaceans. Supplementary References. S1-S4 Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

Citations Over TimeTop 14% of 2015 papers

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