Evidence map›Paper›PMID 8118101›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society1993

High-resolution mapping of a minor histocompatibility antigen gene on mouse chromosome 2.

A R Zuberi, D C Roopenian

Abstract read
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In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

  1. Article
  2. Structure and polymorphism of the mouse prion protein gene.Proceedings of the National Academy of Sciences of the United States of America · 1994
    Article
  3. Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice.Proceedings of the National Academy of Sciences of the United States of America · 1994
    Article
  4. 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

2 authors.

A R ZuberiJackson Laboratory, Bar Harbor, Maine 04609.
D C Roopenian

Funding

NON H-2 HISTOCOMPATIBILITY GENES AND ANTIGENSR01AI028802 · NIAID · JACKSON LABORATORY · PI ROOPENIAN, DERRY CHARLES · 1990 to 2007
$2.1M
EXPERIMENTAL HEMATOLOGY-IMMUNOLOGYT32DK007449 · NIDDK · JACKSON LABORATORY · PI HARRISON, DAVID E · 1986 to 2012
$1.4M
MOLECULAR GENETICS AND MECHANISM OF PROTEIN ANTIBIOTICSR01AI024454 · NIAID · UNIVERSITY OF MARYLAND COLLEGE PK CAMPUS · PI HANSEN, J NORMAN · 1987 to 2001
$344k
MOLECULAR GENETICS &MECHANISM OF PROTEIN ANTIBIOTICSR55AI024454 · NIAID · UNIVERSITY OF MARYLAND COLLEGE PK CAMPUS · PI HANSEN, J NORMAN · 1991 to 1991
–
NIAID NIH HHS AI24454NIAID NIH HHS AI28802NIDDK NIH HHS DK07449
6 · The paper itself

Abstract

Minor histocompatibility (H) loci are significant tissue transplantation barriers but are poorly understood at the genetic and molecular level. We describe the construction of a high-resolution genetic map that positions a class II MHC-restricted minor H antigen locus and orders 12 other genes and genetic markers within the we-un interval of mouse Chromosome (Chr) 2. An intersubspecific backcross between B10.UW/Sn-H-3b and CAST/Ei, an inbred stock of Mus musculus castaneus, was used for this purpose. A total of 1168 backcross mice were generated, and 71 we-un recombinants were identified. Significant compression of the genetic map in males versus females and transmission distortion of CAST-derived we, un, and Aw genes were observed. Monoclonal T cell lines specific for two minor H alloantigens, Hd-1a and Hd-2a, encoded by gene(s) that map to the we-un interval were used to antigen type the backcross mice. The results suggest the Hd-1a and Hd-2a antigens are most likely encoded by a single gene, now referred to as H-3b. The determined gene order is we-0.09 +/- 0.09-Itp-0.62 +/- 0.23-D2Mit77-0.26 +/- 0.15-[Evi-4, Pcna, Prn-p]-0.26 +/- 0.15-Scg-1-0.44 +/- 0.19-[Bmp2a, D2Mit70]-0.09 +/-. 0.09-[D2Mit19, D2Mit46]-1.59 +/- 0.36-D2Mit28-0.97 +/- 0.28-D2Ler1-1.50 +/- 0.35-H-3b-0.26 +/- 0.15-un (% recombination +/- 1 SE). Because the average resolution of the backcross is 0.09 cM, the backcross panel should facilitate the physical mapping and molecular identification of a number of genes in this chromosome region.

Indexed as

Chromosome MappingAnimalsCrosses, GeneticFemaleHeterozygoteMaleMiceMice, Inbred StrainsMinor Histocompatibility AntigensPolymorphism, GeneticRecombination, GeneticMinor Histocompatibility Antigens

Identifiers

PMID8118101

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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.