Evidence map›Paper›PMID 15045471›Full record

ArticleImmunogenetics2004

Murine MHC class Ib gene, H2-M2, encodes a conserved surface-expressed glycoprotein.

Yuki F Moore, Doris Lambracht-Washington, Piotr Tabaczewski, Kirsten Fischer Lindahl

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Immunogenetics, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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.

Yuki F MooreHoward Hughes Medical Institute and Center for Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9050, USA.
Doris Lambracht-Washington
Piotr Tabaczewski
Kirsten Fischer Lindahl

Funding

STRUCTURE AND FUNCTION OF MHC CLASS IB HAPLOTYPESP01AI037818 · NIAID · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI FORMAN, JAMES M · 1995 to 2002
$1.9M
NIAID NIH HHS AI 37818
6 · The paper itself

Abstract

We have determined the genomic sequence of H2-M2 in seven haplotypes from nine inbred strains of mice and in five wild-derived haplotypes. Except for the spretus haplotype sp1 with a premature stop codon, we found only limited polymorphism. Four of the five amino acid substitutions in the alpha-helices are at positions that would point out from the antigen-binding groove, indicating that the polymorphism might influence receptor recognition rather than antigen binding. The rat homologue, RT1.M2(lv1), has 89% identity to H2-M2 at the nucleotide level and 91% at the amino acid level, and it also encodes an intact MHC class I glycoprotein. Chimeric proteins with alpha(1)alpha(2) or alpha(3)-transmembrane domains encoded by H2-Q9 were detectable on the surface of transfectants with monoclonal antibodies against Qa2, and the full-length M2 protein, labeled by fusion with green fluorescent protein, was detectable with S19.8 monoclonal antibodies. The H2-M2 protein was thus expressed on the cell surface, even in TAP-deficient RMA-S cells at 37 degrees C, suggesting that it is TAP-independent. We conclude that H2-M2 is a conserved mouse class Ib gene that is translated to a surface-expressed MHC class I molecule with a function still to be elucidated.

Indexed as

Genes, MHC Class IAlternative SplicingAmino Acid SequenceAnimalsBase SequenceCloning, MolecularConserved SequenceDNA, ComplementaryHeLa CellsHistocompatibility AntigensHistocompatibility Antigens Class IIHumansMembrane GlycoproteinsMiceMice, Inbred StrainsMolecular Sequence DataDNA, ComplementaryH2-M antigensHistocompatibility AntigensHistocompatibility Antigens Class IIhistocompatibility antigens RT, ratMembrane GlycoproteinsRecombinant Fusion Proteins

Identifiers

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.