Literature DB >> 25888517

A comprehensive analysis of teleost MHC class I sequences.

Unni Grimholt1, Kentaro Tsukamoto2, Teruo Azuma3, Jong Leong4, Ben F Koop5, Johannes M Dijkstra6.   

Abstract

BACKGROUND: MHC class I (MHCI) molecules are the key presenters of peptides generated through the intracellular pathway to CD8-positive T-cells. In fish, MHCI genes were first identified in the early 1990's, but we still know little about their functional relevance. The expansion and presumed sub-functionalization of cod MHCI and access to many published fish genome sequences provide us with the incentive to undertake a comprehensive study of deduced teleost fish MHCI molecules.
RESULTS: We expand the known MHCI lineages in teleosts to five with identification of a new lineage defined as P. The two lineages U and Z, which both include presumed peptide binding classical/typical molecules besides more derived molecules, are present in all teleosts analyzed. The U lineage displays two modes of evolution, most pronouncedly observed in classical-type alpha 1 domains; cod and stickleback have expanded on one of at least eight ancient alpha 1 domain lineages as opposed to many other teleosts that preserved a number of these ancient lineages. The Z lineage comes in a typical format present in all analyzed ray-finned fish species as well as lungfish. The typical Z format displays an unprecedented conservation of almost all 37 residues predicted to make up the peptide binding groove. However, also co-existing atypical Z sub-lineage molecules, which lost the presumed peptide binding motif, are found in some fish like carps and cavefish. The remaining three lineages, L, S and P, are not predicted to bind peptides and are lost in some species.
CONCLUSIONS: Much like tetrapods, teleosts have polymorphic classical peptide binding MHCI molecules, a number of classical-similar non-classical MHCI molecules, and some members of more diverged MHCI lineages. Different from tetrapods, however, is that in some teleosts the classical MHCI polymorphism incorporates multiple ancient MHCI domain lineages. Also different from tetrapods is that teleosts have typical Z molecules, in which the residues that presumably form the peptide binding groove have been almost completely conserved for over 400 million years. The reasons for the uniquely teleost evolution modes of peptide binding MHCI molecules remain an enigma.

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Year:  2015        PMID: 25888517      PMCID: PMC4364491          DOI: 10.1186/s12862-015-0309-1

Source DB:  PubMed          Journal:  BMC Evol Biol        ISSN: 1471-2148            Impact factor:   3.260


  91 in total

1.  Mhc class I gene of African lungfish.

Authors:  A Sato; H Sültmann; W E Mayer; J Klein
Journal:  Immunogenetics       Date:  2000-05       Impact factor: 2.846

2.  Spidey: a tool for mRNA-to-genomic alignments.

Authors:  S J Wheelan; D M Church; J M Ostell
Journal:  Genome Res       Date:  2001-11       Impact factor: 9.043

3.  Classical MHC class I genes composed of highly divergent sequence lineages share a single locus in rainbow trout (Oncorhynchus mykiss).

Authors:  Kazuhiko Aoyagi; Johannes M Dijkstra; Chun Xia; Ikuo Denda; Mitsuru Ototake; Keiichiro Hashimoto; Teruyuki Nakanishi
Journal:  J Immunol       Date:  2002-01-01       Impact factor: 5.422

4.  Thermodynamic stability of HLA-B*2705. Peptide complexes. Effect of peptide and major histocompatibility complex protein mutations.

Authors:  S Dédier; S Reinelt; T Reitinger; G Folkers; D Rognan
Journal:  J Biol Chem       Date:  2000-09-01       Impact factor: 5.157

5.  Ab initio gene finding in Drosophila genomic DNA.

Authors:  A A Salamov; V V Solovyev
Journal:  Genome Res       Date:  2000-04       Impact factor: 9.043

6.  Modes of salmonid MHC class I and II evolution differ from the primate paradigm.

Authors:  B P Shum; L Guethlein; L R Flodin; M A Adkison; R P Hedrick; R B Nehring; R J Stet; C Secombes; P Parham
Journal:  J Immunol       Date:  2001-03-01       Impact factor: 5.422

7.  A contig map of the Mhc class I genomic region in the zebrafish reveals ancient synteny.

Authors:  V Michalová; B W Murray; H Sültmann; J Klein
Journal:  J Immunol       Date:  2000-05-15       Impact factor: 5.422

8.  Characterization of the MHC class I region of the Japanese pufferfish (Fugu rubripes).

Authors:  M S Clark; L Shaw; A Kelly; P Snell; G Elgar
Journal:  Immunogenetics       Date:  2001       Impact factor: 2.846

9.  Major histocompatibility complex and immunoglobulin loci visualized by in situ hybridization on Xenopus chromosomes.

Authors:  M Courtet; M Flajnik; L Du Pasquier
Journal:  Dev Comp Immunol       Date:  2001-03       Impact factor: 3.636

10.  Nucleotide sequence of the MHC class I genomic region of a teleost, the medaka (Oryzias latipes).

Authors:  Megumi Y Matsuo; Shuichi Asakawa; Nobuyoshi Shimizu; Hiroshi Kimura; Masaru Nonaka
Journal:  Immunogenetics       Date:  2002-01-29       Impact factor: 2.846

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  37 in total

Review 1.  MHC and adaptive immunity in teleost fishes.

Authors:  Anthony B Wilson
Journal:  Immunogenetics       Date:  2017-07-10       Impact factor: 2.846

Review 2.  Ancient features of the MHC class II presentation pathway, and a model for the possible origin of MHC molecules.

Authors:  Johannes M Dijkstra; Takuya Yamaguchi
Journal:  Immunogenetics       Date:  2018-10-30       Impact factor: 2.846

3.  Comparative MHC nomenclature: report from the ISAG/IUIS-VIC committee 2018.

Authors:  Keith T Ballingall; Ronald E Bontrop; Shirley A Ellis; Unni Grimholt; John A Hammond; Chak-Sum Ho; Jim Kaufman; Lorna J Kennedy; Giuseppe Maccari; Donald Miller; James Robinson; Steven G E Marsh
Journal:  Immunogenetics       Date:  2018-07-24       Impact factor: 2.846

4.  Distribution of ancient α1 and α2 domain lineages between two classical MHC class I genes and their alleles in grass carp.

Authors:  Zibin Li; Nan Zhang; Lizhen Ma; Zehui Qu; Xiaohui Wei; Zixin Liu; Minghu Tang; Nianzhi Zhang; Yinan Jiang; Chun Xia
Journal:  Immunogenetics       Date:  2019-04-02       Impact factor: 2.846

5.  Alternative haplotypes of antigen processing genes in zebrafish diverged early in vertebrate evolution.

Authors:  Sean C McConnell; Kyle M Hernandez; Dustin J Wcisel; Ross N Kettleborough; Derek L Stemple; Jeffrey A Yoder; Jorge Andrade; Jill L O de Jong
Journal:  Proc Natl Acad Sci U S A       Date:  2016-08-04       Impact factor: 11.205

6.  Conservation of sequence motifs suggests that the nonclassical MHC class I lineages CD1/PROCR and UT were established before the emergence of tetrapod species.

Authors:  Johannes M Dijkstra; Takuya Yamaguchi; Unni Grimholt
Journal:  Immunogenetics       Date:  2017-12-21       Impact factor: 2.846

7.  Evolution of the immune system influences speciation rates in teleost fishes.

Authors:  Martin Malmstrøm; Michael Matschiner; Ole K Tørresen; Bastiaan Star; Lars G Snipen; Thomas F Hansen; Helle T Baalsrud; Alexander J Nederbragt; Reinhold Hanel; Walter Salzburger; Nils C Stenseth; Kjetill S Jakobsen; Sissel Jentoft
Journal:  Nat Genet       Date:  2016-08-22       Impact factor: 38.330

Review 8.  A cold-blooded view of adaptive immunity.

Authors:  Martin F Flajnik
Journal:  Nat Rev Immunol       Date:  2018-07       Impact factor: 53.106

Review 9.  Coevolution of MHC genes (LMP/TAP/class Ia, NKT-class Ib, NKp30-B7H6): lessons from cold-blooded vertebrates.

Authors:  Yuko Ohta; Martin F Flajnik
Journal:  Immunol Rev       Date:  2015-09       Impact factor: 12.988

10.  A nonclassical MHC class I U lineage locus in zebrafish with a null haplotypic variant.

Authors:  Hayley Dirscherl; Jeffrey A Yoder
Journal:  Immunogenetics       Date:  2015-08-09       Impact factor: 2.846

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