Cloning of the β2-microglobulin gene in the zebrafish

Hideki Ono, Felipe Figueroa, Colm O'hUigin, Jan Klein

Research output: Contribution to journalArticle

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Abstract

The β2-microglobulin (β2m) is a protein found in the serum in a free form and on the cell surface in a form noncovalently associated with the α chain of the class I major histocompatibility complex (Mhc) molecules. In mammals, the β2m-encoding gene (B2m) is found on a chromosome different from the Mhc proper. We have isolated and characterized the B2m gene of the zebrafish, Brachydanio rerio, family Cyprinidae. We obtained both cDNA and genomic clones of the Brre-B2m gene. The cDNA clones contained the entire coding sequence, the entire 3′ untranslated (UT) region, and at least part of the 5′UT region. The genomic clone contained the entire Brre-B2m gene. The coding sequence specifies 97 amino acid residues of the mature protein so that the zebrafish β2m is two residues shorter than human and one residue shorter than cattle, fowl, or turkey β2m (codons at positions 85 and 86 have been deleted in the Brre-B2m. gene). The amino acid and nucleotide sequence similarities between zebrafish and human β2m (B2m) are 45% and 59%, respectively. Approximately 24% of the positions are invariant and an additional 9% show only conservative substitutions in comparisons which include all known β2m sequences (fish, avian, and mammalian). Most of the conserved positions are in the β strands (some 47% of the β-strand positions are conserved in the three vertebrate classes). The Brre-B2m gene consists of four exons separated by three introns. All of the introns are considerably shorter than the corresponding introns in the mammalian B2m genes. The coding sequences of the cDNA and the genomic clones are almost identical but the sequences of the 3'UT regions differ at 1.7% of the sites, suggesting that the genes borne by these clones might have diverged at least 0.7 million years (my) ago. In contrast to the human B2m gene, the Brre-B2m gene shows no bias in the distribution of the CpG dinucleotides: the dinucleotides are distributed evenly along the entire available sequence. The haploid genome of the zebrafish contains only one copy of the B2m gene.

Original languageEnglish (US)
Pages (from-to)1-10
Number of pages10
JournalImmunogenetics
Volume38
Issue number1
DOIs
StatePublished - Jan 1 1993

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Zebrafish
Organism Cloning
Genes
Clone Cells
Introns
Complementary DNA
3' Untranslated Regions
Major Histocompatibility Complex
Zebrafish Proteins
Cyprinidae
Haploidy
Codon
Vertebrates
Mammals
Amino Acid Sequence
Exons
Fishes
Chromosomes
Genome
Amino Acids

All Science Journal Classification (ASJC) codes

  • Immunology
  • Genetics

Cite this

Ono, H., Figueroa, F., O'hUigin, C., & Klein, J. (1993). Cloning of the β2-microglobulin gene in the zebrafish. Immunogenetics, 38(1), 1-10. https://doi.org/10.1007/BF00216384
Ono, Hideki ; Figueroa, Felipe ; O'hUigin, Colm ; Klein, Jan. / Cloning of the β2-microglobulin gene in the zebrafish. In: Immunogenetics. 1993 ; Vol. 38, No. 1. pp. 1-10.
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Ono, H, Figueroa, F, O'hUigin, C & Klein, J 1993, 'Cloning of the β2-microglobulin gene in the zebrafish', Immunogenetics, vol. 38, no. 1, pp. 1-10. https://doi.org/10.1007/BF00216384

Cloning of the β2-microglobulin gene in the zebrafish. / Ono, Hideki; Figueroa, Felipe; O'hUigin, Colm; Klein, Jan.

In: Immunogenetics, Vol. 38, No. 1, 01.01.1993, p. 1-10.

Research output: Contribution to journalArticle

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N2 - The β2-microglobulin (β2m) is a protein found in the serum in a free form and on the cell surface in a form noncovalently associated with the α chain of the class I major histocompatibility complex (Mhc) molecules. In mammals, the β2m-encoding gene (B2m) is found on a chromosome different from the Mhc proper. We have isolated and characterized the B2m gene of the zebrafish, Brachydanio rerio, family Cyprinidae. We obtained both cDNA and genomic clones of the Brre-B2m gene. The cDNA clones contained the entire coding sequence, the entire 3′ untranslated (UT) region, and at least part of the 5′UT region. The genomic clone contained the entire Brre-B2m gene. The coding sequence specifies 97 amino acid residues of the mature protein so that the zebrafish β2m is two residues shorter than human and one residue shorter than cattle, fowl, or turkey β2m (codons at positions 85 and 86 have been deleted in the Brre-B2m. gene). The amino acid and nucleotide sequence similarities between zebrafish and human β2m (B2m) are 45% and 59%, respectively. Approximately 24% of the positions are invariant and an additional 9% show only conservative substitutions in comparisons which include all known β2m sequences (fish, avian, and mammalian). Most of the conserved positions are in the β strands (some 47% of the β-strand positions are conserved in the three vertebrate classes). The Brre-B2m gene consists of four exons separated by three introns. All of the introns are considerably shorter than the corresponding introns in the mammalian B2m genes. The coding sequences of the cDNA and the genomic clones are almost identical but the sequences of the 3'UT regions differ at 1.7% of the sites, suggesting that the genes borne by these clones might have diverged at least 0.7 million years (my) ago. In contrast to the human B2m gene, the Brre-B2m gene shows no bias in the distribution of the CpG dinucleotides: the dinucleotides are distributed evenly along the entire available sequence. The haploid genome of the zebrafish contains only one copy of the B2m gene.

AB - The β2-microglobulin (β2m) is a protein found in the serum in a free form and on the cell surface in a form noncovalently associated with the α chain of the class I major histocompatibility complex (Mhc) molecules. In mammals, the β2m-encoding gene (B2m) is found on a chromosome different from the Mhc proper. We have isolated and characterized the B2m gene of the zebrafish, Brachydanio rerio, family Cyprinidae. We obtained both cDNA and genomic clones of the Brre-B2m gene. The cDNA clones contained the entire coding sequence, the entire 3′ untranslated (UT) region, and at least part of the 5′UT region. The genomic clone contained the entire Brre-B2m gene. The coding sequence specifies 97 amino acid residues of the mature protein so that the zebrafish β2m is two residues shorter than human and one residue shorter than cattle, fowl, or turkey β2m (codons at positions 85 and 86 have been deleted in the Brre-B2m. gene). The amino acid and nucleotide sequence similarities between zebrafish and human β2m (B2m) are 45% and 59%, respectively. Approximately 24% of the positions are invariant and an additional 9% show only conservative substitutions in comparisons which include all known β2m sequences (fish, avian, and mammalian). Most of the conserved positions are in the β strands (some 47% of the β-strand positions are conserved in the three vertebrate classes). The Brre-B2m gene consists of four exons separated by three introns. All of the introns are considerably shorter than the corresponding introns in the mammalian B2m genes. The coding sequences of the cDNA and the genomic clones are almost identical but the sequences of the 3'UT regions differ at 1.7% of the sites, suggesting that the genes borne by these clones might have diverged at least 0.7 million years (my) ago. In contrast to the human B2m gene, the Brre-B2m gene shows no bias in the distribution of the CpG dinucleotides: the dinucleotides are distributed evenly along the entire available sequence. The haploid genome of the zebrafish contains only one copy of the B2m gene.

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