Abstract

The velvet belly lanternshark (Etmopterus spinax) is a small deep-sea shark commonly found in the Eastern Atlantic and the Mediterranean Sea. This bioluminescent species is able to emit a blue-green ventral glow used in counter-illumination camouflage, mainly. In this study, paired-end Illumina HiSeqTM technology has been employed to generate transcriptome data from eye and ventral skin tissues of the lanternshark. About 64 and 49 million Illumina reads were generated from skin and eye tissues respectively. The assembly allowed us to predict 119,749 total unigenes including 94,569 for the skin transcriptome and 94,365 for the eye transcriptome while 74,753 were commonly found in both transcriptomes. A taxonomy filtering was applied to extract a reference transcriptome containing 104,390 unigenes among which 38,836 showed significant similarities to known sequences in NCBI non-redundant protein sequences database. Around 58% of the annotated unigenes match with predicted genes from the Elephant shark (Callorhinchus milii) genome. The transcriptome completeness has been evaluated by successfully capturing around 98% of orthologous genes of the « Core eukaryotic gene dataset » within the E. spinax reference transcriptome. We identified potential “light-interacting toolkit” genes including multiple genes related to ocular and extraocular light perception processes such as opsins, phototransduction actors or crystallins. Comparative gene expression analysis reveals eye-specific expression of opsins, ciliary phototransduction actors, crystallins and vertebrate retinoid pathway actors. In particular, mRNAs from a single rhodopsin gene and its potentially associated peropsin were detected in the eye transcriptome, only, confirming a monochromatic vision of the lanternshark. Encephalopsin mRNAs were mainly detected in the ventral skin transcriptome. In parallel, immunolocalization of the encephalopsin within the ventral skin of the shark suggests a functional relation with the photophores, i.e. epidermal light-producing organs. We hypothesize that extraocular photoreception might be involved in the bioluminescence control possibly acting on the shutter opening and/or the photocyte activity itself. The newly generated reference transcriptome provides a valuable resource for further understanding of the shark biology.

Highlights

  • Over the past 450 million years, cartilaginous fish have evolved to fill a large range of predatory niches in marine and freshwater ecosystems [1, 2]

  • For non-model or emerging model marine organisms, next-generation sequencing (NGS) technologies offer a great opportunity for rapid access to genetic information

  • Our study presents the first transcriptomes of the lanternshark E. spinax opening a window on a better understanding of the biology of this species

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Summary

Introduction

Over the past 450 million years, cartilaginous fish have evolved to fill a large range of predatory niches in marine and freshwater ecosystems [1, 2]. Studies reported that the retina of the majority of cartilaginous fishes contains only rod photoreceptors [8, 9]. These organisms were thought to have poor visual acuity with eyes that are specialized for scotopic vision (i.e., dim light condition) with no capacity for photopic vision (i.e., bright light condition) or color discrimination [4]. It was demonstrated that the majority of cartilaginous fishes are able to function under a range of photopic and scotopic light intensities and possess a duplex retina containing both rod and cone photoreceptors [7, 10,11,12,13,14]. Some deep-sea sharks and rajids appear to have all-rod retinas [15,16,17]

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