Literature DB >> 30767303

Phototactic tails: Evolution and molecular basis of a novel sensory trait in sea snakes.

Jenna M Crowe-Riddell1,2, Bruno F Simões1,3, Julian C Partridge4, David M Hunt4,5, Steven Delean1, Julian G Schwerdt1, James Breen6,7,8, Alastair Ludington1,7, David J Gower9, Kate L Sanders1.   

Abstract

Dermal phototaxis has been reported in a few aquatic vertebrate lineages spanning fish, amphibians and reptiles. These taxa respond to light on the skin of their elongate hind-bodies and tails by withdrawing under cover to avoid detection by predators. Here, we investigated tail phototaxis in sea snakes (Hydrophiinae), the only reptiles reported to exhibit this sensory behaviour. We conducted behavioural tests in 17 wild-caught sea snakes of eight species by illuminating the dorsal surface of the tail and midbody skin using cold white, violet, blue, green and red light. Our results confirmed phototactic tail withdrawal in the previously studied Aipysurus laevis, revealed this trait for the first time in A. duboisii and A. tenuis, and suggested that tail photoreceptors have peak spectral sensitivities between blue and green light (457-514 nm). Based on these results, and an absence of photoresponses in five Aipysurus and Hydrophis species, we tentatively infer that tail phototaxis evolved in the ancestor of a clade of six Aipysurus species (comprising 10% of all sea snakes). Quantifying tail damage, we found that the probability of sustaining tail injuries was not influenced by tail phototactic ability in snakes. Gene profiling showed that transcriptomes of both tail skin and body skin lacked visual opsins but contained melanopsin (opn4x) in addition to key genes of the retinal regeneration and phototransduction cascades. This work suggests that a nonvisual photoreceptor (e.g., Gq rhabdomeric) signalling pathway underlies tail phototaxis, and provides candidate gene targets for future studies of this unusual sensory innovation in reptiles.
© 2019 John Wiley & Sons Ltd.

Entities:  

Keywords:  dermal photoreception; dermal phototaxis; extraocular; melanopsin; sea snakes

Mesh:

Substances:

Year:  2019        PMID: 30767303     DOI: 10.1111/mec.15022

Source DB:  PubMed          Journal:  Mol Ecol        ISSN: 0962-1083            Impact factor:   6.185


  5 in total

1.  Inside the head of snakes: influence of size, phylogeny, and sensory ecology on endocranium morphology.

Authors:  Marion Segall; Raphaël Cornette; Arne R Rasmussen; Christopher J Raxworthy
Journal:  Brain Struct Funct       Date:  2021-07-21       Impact factor: 3.270

2.  Ultrastructural evidence of a mechanosensory function of scale organs (sensilla) in sea snakes (Hydrophiinae).

Authors:  Jenna M Crowe-Riddell; Ruth Williams; Lucille Chapuis; Kate L Sanders
Journal:  R Soc Open Sci       Date:  2019-04-10       Impact factor: 2.963

3.  Characterization of the melanopsin gene (Opn4x) of diurnal and nocturnal snakes.

Authors:  Einat Hauzman; Venkatasushma Kalava; Daniela Maria Oliveira Bonci; Dora Fix Ventura
Journal:  BMC Evol Biol       Date:  2019-08-28       Impact factor: 3.260

Review 4.  Melanopsin phototransduction: beyond canonical cascades.

Authors:  Ely Contreras; Alexis P Nobleman; Phyllis R Robinson; Tiffany M Schmidt
Journal:  J Exp Biol       Date:  2021-11-29       Impact factor: 3.312

5.  New Environment, New Invaders-Repeated Horizontal Transfer of LINEs to Sea Snakes.

Authors:  James D Galbraith; Alastair J Ludington; Alexander Suh; Kate L Sanders; David L Adelson
Journal:  Genome Biol Evol       Date:  2020-12-06       Impact factor: 3.416

  5 in total

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