4.3 Article

Holosteans contextualize the role of the teleost genome duplication in promoting the rise of evolutionary novelties in the ray-finned fish innate immune system

Journal

IMMUNOGENETICS
Volume 73, Issue 6, Pages 479-497

Publisher

SPRINGER
DOI: 10.1007/s00251-021-01225-6

Keywords

Bowfin and gar; Multigene families; Diverse immunoglobulin domain-containing proteins (DICPs); Novel immune-type receptors (NITRs); V(D)J recombination; MHC

Funding

  1. National Science Foundation [IOS-1755242, IOS-1755330]
  2. Triangle Center for Evolutionary Medicine (TriCEM)
  3. National Institutes of Health [R01OD011116]

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The study investigates the receptor diversity of two innate immune gene families in the teleost sister lineage, Holostei, providing insights into the evolutionary history and linkage of these gene clusters. The findings reveal a diversity in these immune receptors in Holostei that rivals that of many teleosts, challenging prevailing expectations regarding the consequences of genome duplication during actinopterygian evolution.
Over 99% of ray-finned fishes (Actinopterygii) are teleosts, a clade that comprises half of all living vertebrate species that have diversified across virtually all fresh and saltwater ecosystems. This ecological breadth raises the question of how the immunogenetic diversity required to persist under heterogeneous pathogen pressures evolved. The teleost genome duplication (TGD) has been hypothesized as the evolutionary event that provided the substrate for rapid genomic evolution and innovation. However, studies of putative teleost-specific innate immune receptors have been largely limited to comparisons either among teleosts or between teleosts and distantly related vertebrate clades such as tetrapods. Here we describe and characterize the receptor diversity of two clustered innate immune gene families in the teleost sister lineage: Holostei (bowfin and gars). Using genomic and transcriptomic data, we provide a detailed investigation of the phylogenetic history and conserved synteny of gene clusters encoding diverse immunoglobulin domain-containing proteins (DICPs) and novel immune-type receptors (NITRs). These data demonstrate an ancient linkage of DICPs to the major histocompatibility complex (MHC) and reveal an evolutionary origin of NITR variable-joining (VJ) exons that predate the TGD by at least 50 million years. Further characterizing the receptor diversity of Holostean DICPs and NITRs illuminates a sequence diversity that rivals the diversity of these innate immune receptor families in many teleosts. Taken together, our findings provide important historical context for the evolution of these gene families that challenge prevailing expectations concerning the consequences of the TGD during actinopterygiian evolution.

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