Abstract

Squamates are a diverse order of vertebrates, representing more than 7,000 species. Yet, descriptions of full-length major histocompatibility complex (MHC) genes in this group are nearly absent from the literature, while the number of MHC studies continues to rise in other vertebrate taxa. The lack of basic information about MHC organization in squamates inhibits investigation into the relationship between MHC polymorphism and disease, and leaves a large taxonomic gap in our understanding of amniote MHC evolution. Here, we use both cDNA and genomic sequence data to characterize a class I MHC gene (Amcr-UA) from the Galápagos marine iguana, a member of the squamate subfamily Iguaninae. Amcr-UA appears to be functional since it is expressed in the blood and contains many of the conserved peptide-binding residues that are found in classical class I genes of other vertebrates. In addition, comparison of Amcr-UA to homologous sequences from other iguanine species shows that the antigen-binding portion of this gene is under purifying selection, rather than balancing selection, and therefore may have a conserved function. A striking feature of Amcr-UA is that both the cDNA and genomic sequences lack the transmembrane and cytoplasmic domains that are necessary to anchor the class I receptor molecule into the cell membrane, suggesting that the product of this gene is secreted and consequently not involved in classical class I antigen-presentation. The truncated and conserved character of Amcr-UA lead us to define it as a nonclassical gene that is related to the few available squamate class I sequences. However, phylogenetic analysis placed Amcr-UA in a basal position relative to other published classical MHC genes from squamates, suggesting that this gene diverged near the beginning of squamate diversification.

Highlights

  • Class I major histocompatibility complex (MHC) molecules are well known for their pivotal role in the recognition of altered self cells by T cytotoxic (TC) cells

  • The Tm/Cyt domains are essential for the standard antigen presentation function of class I molecules because they anchor the receptor structure into the cell membrane of altered selfcells where they can be recognized by CD8+ TC cells [1,2]

  • In the Amcr-UA Complementary DNA (cDNA) sequence, the Tm/Cyt domains are largely missing, except for an 11 amino acid extension of the a-3 domain that is followed by a stop codon

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Summary

Introduction

Class I major histocompatibility complex (MHC) molecules are well known for their pivotal role in the recognition of altered self cells (e.g. virus-infected cells) by T cytotoxic (TC) cells. In this process, short peptide fragments derived from pathogens within the host cell are bound to class I receptor structures and transported to the cell surface. An additional characteristic of the genes encoding class I receptors is a high level of polymorphism, which enables the host to recognize and bind a wide array of foreign peptides [4]. As the number of descriptions of vertebrate MHC loci has increased, it has become clear that many class I genes do not possess the features described above

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