PUBLICATION

A contig map of the mhc class I genomic region in the zebrafish reveals ancient synteny

Authors
Michalova, V., Murray, B.W., Sültmann, H., and Klein, J.
ID
ZDB-PUB-000510-8
Date
2000
Source
Journal of immunology (Baltimore, Md. : 1950)   164(10): 5296-5305 (Journal)
Registered Authors
Klein, Jan, Sültmann, Holger
Keywords
none
MeSH Terms
  • Animals
  • Bacteriophage P1/genetics
  • Base Sequence
  • Chromosomes, Artificial, Yeast/genetics
  • Chromosomes, Bacterial/genetics
  • Cloning, Molecular
  • Contig Mapping*
  • Evolution, Molecular
  • Genes, MHC Class I*
  • Genes, MHC Class II
  • Genetic Linkage/immunology
  • Genetic Markers
  • Humans
  • Major Histocompatibility Complex/genetics*
  • Molecular Sequence Data
  • Multigene Family/immunology
  • Sequence Homology, Nucleic Acid*
  • Zebrafish/genetics*
  • Zebrafish/immunology*
PubMed
10799891 Full text @ J. Immunol.
Abstract
In contrast to the human and mouse Mhc, in which the clusters of class I and class II loci reside in close vicinity to one another, in the zebrafish, Danio rerio, they are found in different linkage groups. Chromosome walking using BAC (bacterial artificial chromosome) and PAC (P1 artificial chromosome) clones reveals the zebrafish class I region to occupy a segment of approximately 450 kb and to encompass at least 19 loci. These include three class I (Dare-UDA, -UEA, -UFA), five proteasome subunit beta (PSMB8, -9A, -9C, -11, -12), two TAPs (TAP2A, TAP2B), and one TAP binding protein (TAPBP). This arrangement contrasts with the arrangements found in human and mouse Mhc, in which the orthologues of the PSMB, TAP, and TAPBP loci reside within the class II region. In addition to this main zebrafish class I contig, a shorter contig of about 150 kb contains two additional class I (UBA, UCA) and at least five other loci. It probably represents a different haplotype of part of the class I region. The previously identified UAA gene shares an identical 5' part with UEA, but the two genes differ in their 3' parts. One of them is probably the result of an unequal crossing over. The described organization has implications for the persistence of syntenic relationships, coevolution of loci, and interpretation of the origin of the human/mouse Mhc organization.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping