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Major histocompatibility complex in Osteichthyes Cover

Major histocompatibility complex in Osteichthyes

Open Access
|Mar 2020

Figures & Tables

Table 1

MHC class I and II gene loci in Atlantic salmon (5, 13) (a) against the background of the relevant data for humans (b)

(a)
Chr.*MHC I genes in Salmo salar (Sasa) (MhcSasa-U… or Z, S, L, P…)*MHC II genes in Salmo salar (Sasa) (MhcSasa-D…)
2NoneDCB1, DCA / DEA, DEB / DCB2
5NoneDEAψ, DEBψ
7PAAψNone
9SAANone
10LKAψNone
11LCA, LCAψNone
12LDADDA, DDB / **DAA, DAB1
13NoneDBB, DBA
14UDA1, UCA2 / UCA1, UGA / ZBAb, ZCAb, ZDAbψNone
20SAAψNone
21LIA / UHA1, UHA2None
22NoneDABψ
25LIAψ / LLAψNone
26LFA, LGA, LHANone
27ULA, **UBA, ZAAa, ZBAa, ZCAa, ZDAaNone
(b)
Chr.MHC I genes in humansMHC II genes in humans
6**HLA-A, HLA-B, HLA-C HLA-E, HLA-F, HLA-G, MICA and MICB**HLA-DP, HLA-DQ and HLA-DR HLA-DM and HLA-DO

Chr. – chromosome no.; symbol ( / ) – divides genes with separate loci;

* – the constituents of the nomenclature of MHC class I and class II genes are listed in Tables 2 and 4;

* – the constituents of the nomenclature of MHC class I and class II genes are listed in Tables 2 and 4;

** – genes of the classical MHC molecules

** – genes of the classical MHC molecules

** – genes of the classical MHC molecules

** – genes of the classical MHC molecules

Table 2

Constituents of the nomenclature of MHC class I genes (table cells with grey underlay) in fish on the example of Atlantic salmon (11, 13)

MHCFish genus and species symbolMHC class I gene lineageMHC class I gene sublineageLocusSubclassGeneFull name / symbol of gene
BUBA**MhcSasa-UBA
CUCA1***, UCA2MhcSasa-UCA1, MhcSasa-UCA2
DUDA1MhcSasa-UDA1
GUGAMhcSasa-UGA
UNoneHUHA1, UHA2MhcSasa-UHA1, MhcSasa-UHA2
AZAAaMhcSasa-ZAAa
BZBAa, ZBAbMhcSasa-ZBAa, MhcSasa-ZBAb
ZZ1*CZCAa, ZCAbMhcSasa-ZCAa, MhcSasa-ZCAb
CLCA, LCAψMhcSasa-LCA, MhcSasa-LCAψ
DLDAMhcSasa-LDA
FLFAMhcSasa-LFA
GLGAMhcSasa-LGA
HLHAMhcSasa-LHA
LNoneILIA, LIAψMhcSasa-LIA, LIAψ
KLKAψMhcSasa-LKAψ
PNoneAPAAψMhcSasa-PAAψ

** – a gene of an MHC Ia molecule;

*** – locus no.;

* – sublineage Z1 with a typical sequence, isolated in, inter alia, Salmo salar;

ψ – pseudogenes

ψ – pseudogenes

ψ – pseudogenes

ψ – pseudogenes

ψ – pseudogenes

ψ – pseudogenes

ψ – pseudogenes

ψ – pseudogenes

ψ – pseudogenes

ψ – pseudogenes

ψ – pseudogenes

ψ – pseudogenes

ψ – pseudogenes

ψ – pseudogenes

Table 3

Occurrence of MHC I and MHC II genes in selected species of Osteichthyes (11, 13)

Lungfish (subclass Dipnoi)x*
Paddlefish (family Polyodontidae)xx
Sturgeon (family Acipenseridae)xx*x
Spotted gar (Lepisosteus oculatus)xx*0xxxx
Zebrafish (Danio rerio)xx0x0xx0
Carp (Cyprinus carpio)xxxxx
Mexican tetra (Astyanax mexicanus)xxxxxx
Atlantic salmon (Salmo salar)xxxxxxxx
Medaka (Oryzias latipes)xx000xx0
Stickleback (Gasterosteus aculeatus)xx000xx0

symbol ( – ) – lack of sufficient data to deduce that MHC genes of a specific lineage or sublineage are present or absent; 0 – lack of MHC genes of a specific lineage or sublineage; x – occurrence of MHC genes of a specific lineage or sublineage

* – lineage Z;

* – lineage Z;

* – lineage Z;

Table 4

Constituents of the nomenclature of MHC class II genes (table cells with grey underlay) in fish on the example of Salmo salar and Oryzias latipes

MHCFish genus and species symbolMHC class II gene lineageMHC class II gene sublineageLocusSubclassGeneFull name / symbol of gene
A*DAADABMhcOrla-DAADAB
E**DEADEBMhcOrla-DEADEB

* – genes of the classical MHC II molecule;

*** – pairs of Oryzias latipes genes with limited expression and low polymorphism, clustering in sublineage A (5)

*** – pairs of Oryzias latipes genes with limited expression and low polymorphism, clustering in sublineage A (5)

** – gene clustering based on the domain α1 sequence, according to Dijkstra et al. (5) and Grimholt (11), with preservation of sublineage E for sequences making up a cluster with DEA–DEB in Salmo salar and with creation of sublineage B with sequences forming a cluster with DEA–DEB in Oryzias latipes;

** – gene clustering based on the domain α1 sequence, according to Dijkstra et al. (5) and Grimholt (11), with preservation of sublineage E for sequences making up a cluster with DEA–DEB in Salmo salar and with creation of sublineage B with sequences forming a cluster with DEA–DEB in Oryzias latipes;

Table 5

Genes from selected MHC regions, identified in humans and fish (5, 13)

HumansSpotted garAtlantic salmonShared genes**
MHC IMHC IIMHC IMHC IIMHC IMHC IIMHC IMHC II***
HLA-GHLA-DRαU (3 loci) (2 loci)U*PSMB8PBX2
HLA-AHLA-DRβP (3 loci) (2 loci)TUBBTAP1
HLA-EHLA-DQαL (2 loci)A/BαFLOT1RGL2
HLA-CHLA-DQβu.s.A/BβTCF19PHF1
HLA-BHLA-DPαu.s. αTAP2BRD2
HLA-DPβPSMB9SYNGAP-like
HLA-DMαBRD2
HLA-DMβTAPBP
HLA-DoαRXRB
HLA-DoβHSD17B8
PSMB10

u.s. – undefined sequence; PSMB8 – protein-coding gene, proteasome subunit β type-8; TUBB – protein-coding gene, tubulin β-chain; FLOT1 – protein-coding gene, flotillin-1; TCF19 – protein-coding gene, transcription factor 19; TAP2 – protein-coding gene, antigen peptide transporter 2; PSMB9 – protein-coding gene, proteasome subunit β type-9; BRD2 – protein-coding gene, bromodomain-containing protein 2; TAPBP – protein-coding gene, TAP-associated glycoprotein, also known as tapasin; RXRB – gene, retinoid X reflex point β (RXR-β); HSD17B8 – enzyme, oestradiol 17 β-dehydrogenase 8; PSMB10 – protein coding gene, proteasome subunit β type-10; PBX2 – protein-coding gene, pre-B-cell leukaemia transcription factor 2; TAP1 – protein-coding gene, transporter associated with antigen processing 1; RGL2 – protein-coding gene, ral guanine nucleotide dissociation stimulator-like 2; PHF1 – protein-coding gene, PHD finger protein 1; SYNGAP-like – Ras GTPase-activating protein SynGap-like;

** – selected genes shared by humans (MHC region sized ~ 4Mb) and Salmo salar (MHC I and MHC II), as well as by Danio rerio and Oryzias latipes (MHC I);

*** – genes occurring within sublineage E in Salmonidae

* – syntenic gene;

DOI: https://doi.org/10.2478/jvetres-2020-0025 | Journal eISSN: 2450-8608 (formerly 2300-3235)
Language: English
Page range: 127 - 136
Submitted on: Aug 16, 2019
Accepted on: Mar 6, 2020
Published on: Mar 24, 2020
Published by: National Veterinary Research Institute in Pulawy
In partnership with: Paradigm Publishing Services

© 2020 Michał Stosik, Beata Tokarz-Deptuła, Wiesław Deptuła, published by National Veterinary Research Institute in Pulawy
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.