» Articles » PMID: 20614118

A Molecule in Teleost Fish, Related with Human MHC-encoded G6F, Has a Cytoplasmic Tail with ITAM and Marks the Surface of Thrombocytes and in Some Fishes Also of Erythrocytes

Overview
Journal Immunogenetics
Date 2010 Jul 9
PMID 20614118
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

In teleost fish, a novel gene G6F-like was identified, encoding a type I transmembrane molecule with four extracellular Ig-like domains and a cytoplasmic tail with putative tyrosine phosphorylation motifs including YxN and an immunoreceptor tyrosine-based activation motif (ITAM). G6F-like maps to a teleost genomic region where stretches corresponding to human chromosomes 6p (with the MHC), 12p (with CD4 and LAG-3), and 19q are tightly linked. This genomic organization resembles the ancestral "Ur-MHC" proposed for the jawed vertebrate ancestor. The deduced G6F-like molecule shows sequence similarity with members of the CD4/LAG-3 family and with the human major histocompatibility complex-encoded thrombocyte marker G6F. Despite some differences in molecular organization, teleost G6F-like and tetrapod G6F seem orthologous as they map to similar genomic location, share typical motifs in transmembrane and cytoplasmic regions, and are both expressed by thrombocytes/platelets. In the crucian carps goldfish (Carassius auratus auratus) and ginbuna (Carassius auratus langsdorfii), G6F-like was found expressed not only by thrombocytes but also by erythrocytes, supporting that erythroid and thromboid cells in teleost fish form a hematopoietic lineage like they do in mammals. The ITAM-bearing of G6F-like suggests that the molecule plays an important role in cell activation, and G6F-like expression by erythrocytes suggests that these cells have functional overlap potential with thrombocytes.

Citing Articles

CD4 and LAG-3 from sharks to humans: related molecules with motifs for opposing functions.

Takizawa F, Hashimoto K, Miyazawa R, Ohta Y, Verissimo A, Flajnik M Front Immunol. 2024; 14:1267743.

PMID: 38187381 PMC: 10768021. DOI: 10.3389/fimmu.2023.1267743.


Structural Comparison Between MHC Classes I and II; in Evolution, a Class-II-Like Molecule Probably Came First.

Wu Y, Zhang N, Hashimoto K, Xia C, Dijkstra J Front Immunol. 2021; 12:621153.

PMID: 34194421 PMC: 8236899. DOI: 10.3389/fimmu.2021.621153.


Major Histocompatibility Complex (MHC) Genes and Disease Resistance in Fish.

Yamaguchi T, Dijkstra J Cells. 2019; 8(4).

PMID: 31027287 PMC: 6523485. DOI: 10.3390/cells8040378.


Nucleated red blood cells: Immune cell mediators of the antiviral response.

Nombela I, Ortega-Villaizan M PLoS Pathog. 2018; 14(4):e1006910.

PMID: 29698529 PMC: 5919432. DOI: 10.1371/journal.ppat.1006910.


The identification of additional zebrafish DICP genes reveals haplotype variation and linkage to MHC class I genes.

Rodriguez-Nunez I, Wcisel D, Litman R, Litman G, Yoder J Immunogenetics. 2016; 68(4):295-312.

PMID: 26801775 PMC: 7188334. DOI: 10.1007/s00251-016-0901-6.


References
1.
Jagadeeswaran P, Lin S, Weinstein B, Hutson A, Kim S . Loss of GATA1 and gain of FLI1 expression during thrombocyte maturation. Blood Cells Mol Dis. 2010; 44(3):175-80. PMC: 2829368. DOI: 10.1016/j.bcmd.2009.12.012. View

2.
Trowsdale J . Genetic and functional relationships between MHC and NK receptor genes. Immunity. 2001; 15(3):363-74. DOI: 10.1016/s1074-7613(01)00197-2. View

3.
Kasahara M . The chromosomal duplication model of the major histocompatibility complex. Immunol Rev. 1999; 167:17-32. DOI: 10.1111/j.1600-065x.1999.tb01379.x. View

4.
Kammerer R, Zimmermann W . Coevolution of activating and inhibitory receptors within mammalian carcinoembryonic antigen families. BMC Biol. 2010; 8:12. PMC: 2832619. DOI: 10.1186/1741-7007-8-12. View

5.
Panagos P, Dobrinski K, Chen X, Grant A, Traver D, Djeu J . Immune-related, lectin-like receptors are differentially expressed in the myeloid and lymphoid lineages of zebrafish. Immunogenetics. 2006; 58(1):31-40. DOI: 10.1007/s00251-005-0064-3. View