Evidence map›Paper›PMID 8462988›Full record

ArticleImmunogenetics1993

Cloning of the beta 2-microglobulin gene in the zebrafish.

H Ono, F Figueroa, C O'hUigin, J Klein

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Immunogenetics, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.5field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Frontiers in immunology · 2024
    Article
  3. Methodological considerations for aqueous environmental RNA collection, preservation, and extraction.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2023
    Article
  4. Article
  5. Review
  6. Article
  7. Primordial linkage of β2-microglobulin to the MHC.Journal of immunology (Baltimore, Md. : 1950) · 2011
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. The conundrum of nonclassical major histocompatibility complex genes.Proceedings of the National Academy of Sciences of the United States of America · 1994
    Review
  19. Isolation and characterization of major histocompatibility complex class IIB genes from the nurse shark.Proceedings of the National Academy of Sciences of the United States of America · 1994
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

H OnoMax-Planck-Institut für Biologie, Abteilung Immungenetik, Tübingen, Germany.
F Figueroa
C O'hUigin
J Klein
Max Planck Institute for Biology · DEUniversity of Miami · US

Funding

POLYMORPHISM OF THE MAJOR HISTOCOMPATIBILITY COMPLEXR01AI023667 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI KLEIN, JAN · 1986 to 1995
–
NIAID NIH HHS AI 23667
6 · The paper itself

Abstract

The beta 2-microglobulin (beta 2m) is a protein found in the serum in a free form and on the cell surface in a form noncovalently associated with the alpha chain of the class I major histocompatibility complex (Mhc) molecules. In mammals, the beta 2m-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 beta 2m is two residues shorter than human and one residue shorter than cattle, fowl, or turkey beta 2m (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 beta 2m (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 beta 2m sequences (fish, avian, and mammalian). Most of the conserved positions are in the beta strands (some 47% of the beta-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.

Indexed as

Amino Acid SequenceAnimalsBase Sequencebeta 2-MicroglobulinCloning, MolecularConsensus SequenceDNAGenesHumansMolecular Sequence DataOligodeoxyribonucleotidesPhylogenyPolymerase Chain ReactionProtein Structure, TertiaryRestriction MappingSequence Alignmentbeta 2-MicroglobulinDNAOligodeoxyribonucleotides

Identifiers

PMID8462988
OpenAlexW1997165401

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.