Abstract

BackgroundThe cartilaginous fishes diverged from other jawed vertebrates ~ 450 million years ago (mya). Despite this key evolutionary position, the only high-quality cartilaginous fish genome available is for the elephant shark (Callorhinchus milii), a chimaera whose ancestors split from the elasmobranch lineage ~ 420 mya. Initial analysis of this resource led to proposals that key components of the cartilaginous fish adaptive immune system, most notably their array of T cell subsets, was primitive compared to mammals. This proposal is at odds with the robust, antigen-specific antibody responses reported in elasmobranchs following immunization. To explore this discrepancy, we generated a multi-tissue transcriptome for small-spotted catshark (Scyliorhinus canicula), a tractable elasmobranch model for functional studies. We searched this, and other newly available sequence datasets, for CD4+ T cell subset-defining genes, aiming to confirm the presence or absence of each subset in cartilaginous fishes.ResultsWe generated a new transcriptome based on a normalised, multi-tissue RNA pool, aiming to maximise representation of tissue-specific and lowly expressed genes. We utilized multiple transcriptomic datasets and assembly variants in phylogenetic reconstructions to unambiguously identify several T cell subset-specific molecules in cartilaginous fishes for the first time, including interleukins, interleukin receptors, and key transcription factors. Our results reveal the inability of standard phylogenetic reconstruction approaches to capture the site-specific evolutionary processes of fast-evolving immune genes but show that site-heterogeneous mixture models can adequately do so.ConclusionsOur analyses reveal that cartilaginous fishes are capable of producing a range of CD4+ T cell subsets comparable to that of mammals. Further, that the key molecules required for the differentiation and functioning of these subsets existed in the jawed vertebrate ancestor. Additionally, we highlight the importance of considering phylogenetic diversity and, where possible, utilizing multiple datasets for individual species, to accurately infer gene presence or absence at higher taxonomic levels.

Highlights

  • The cartilaginous fishes diverged from other jawed vertebrates ~ 450 million years ago

  • All assemblies lack some BUSCOs, the Mulley et al (MEA) assembly contains the fewest missing BUSCOs. Both the MEA and King et al (KEA) datasets were sequenced on the Illumina platform, raising the possibility that the increased number of transcripts in our assemblies is linked to the increased error rates under Ion Torrent sequencing [91, 92]

  • Our results indicate that two IL4/13-like lineages are present and expressed in small-spotted catshark (IL-4/13A and IL4/13B), having duplicated in the ancestor of cartilaginous fishes (BPP = 0.88; Ultrafast Bootstrap (UB) = 77%), but do not support clear orthology of these genes, or those of teleosts, to mammalian IL-4 or IL-13 (Fig. 4b)

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Summary

Introduction

The cartilaginous fishes diverged from other jawed vertebrates ~ 450 million years ago (mya). The cartilaginous fishes (Chondrichthyes) diverged from a common ancestor with other vertebrates around 450 million years ago (mya) and are comprised of Holocephali (chimaeras) and Elasmobranchii (sharks, skates, and rays), which likely split between 300 and 420 mya [1, 2] They represent the most phylogenetically-distant relatives of mammals to have an adaptive immune system based on somatically-rearranging immunoglobulins (i.e. antibodies) and T cell receptors, as well as major histocompatibility complex molecules [3, 4]. T cells expressing the CD4 co-receptor are vital for mounting an adaptive immune response [7], and are loosely split into two major groups:

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