Evidence map›Paper›PMID 1672162›Full record

ArticleJournal of virology1991

Localization of the human gene allowing infection by gibbon ape leukemia virus to human chromosome region 2q11-q14 and to the homologous region on mouse chromosome 2.

M Kaelbling, R Eddy, T B Shows, N G Copeland, D J Gilbert, N A Jenkins, H P Klinger, B O'Hara

Abstract read
In one paragraph

Article in Journal of virology, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Cell-surface receptors for retroviruses and implications for gene transfer.Proceedings of the National Academy of Sciences of the United States of America · 1996
    Review
  6. Review
  7. Article
  8. A human amphotropic retrovirus receptor is a second member of the gibbon ape leukemia virus receptor family.Proceedings of the National Academy of Sciences of the United States of America · 1994
    Article
  9. Cloning of the cellular receptor for amphotropic murine retroviruses reveals homology to that for gibbon ape leukemia virus.Proceedings of the National Academy of Sciences of the United States of America · 1994
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Mouse chromosome 2.Mammalian genome : official journal of the International Mammalian Genome Society · 1992
    Review
  15. Mouse chromosome 2.Mammalian genome : official journal of the International Mammalian Genome Society · 1991
    Review
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

8 authors.

M KaelblingDepartment of Molecular Genetics, Albert Einstein College of Medicine, Bronx, New York 10461.
R Eddy
T B Shows
N G Copeland
D J Gilbert
N A Jenkins
H P Klinger
B O'Hara

Funding

PROVIDE BASIC CANCER RESEARCHN01CO074101 · CO · ADVANCED BIOSCIENCE LABORATORIES, INC. · PI VANDE WOUDE, GEORGE F · 1987 to 1994
–
GENE REGULATION &INTERACTION--NORMAL &MALIGNANT CELLR01CA016720 · NCI · YESHIVA UNIVERSITY · PI KLINGER, HAROLD P · 1985 to 1990
–
MOLECULAR CLONING OF RETROVIRAL RECEPTOR GENESR01CA043951 · NCI · YESHIVA UNIVERSITY · PI KLINGER, HAROLD P · 1987 to 1989
–
NCI NIH HHS CA16720NCI NIH HHS CA43951NCI NIH HHS N01-CO-74101
6 · The paper itself

Abstract

Retrovirus receptors remain a largely unexplored group of proteins. Of the receptors which allow infection of human and murine cells by various retroviruses, only three have been identified at the molecular level. These receptors include CD4 for human immunodeficiency virus, Rec-1 for murine ecotropic virus, and GLVR1 for gibbon ape leukemia virus. These three proteins show no homology to one another at the DNA or protein level. Therefore, work to date has not shown any general relationship or structural theme shared by retroviral receptors. Genes for two of these receptors (CD4 and Rec-1) and several others which have not yet been cloned have been localized to specific chromosomes. In order to assess the relationship between GLVR1 and other retroviral receptors, we mapped the chromosome location of GLVR1 in human and mouse. GLVR1 was found to map to human chromosome 2q11-q14 by in situ hybridization and somatic-cell hybrid analysis. This location is distinct from those known for receptors for retroviruses infecting human cells. Glvr-1 was then mapped in the mouse by interspecies backcrosses and found to map to chromosome 2 in a region of linkage conservation with human chromosome 2. This mouse chromosome carries Rec-2, the likely receptor for M813, a retrovirus derived from a feral Asian mouse. These data raise the interesting possibility that Rec-2 and Glvr-1 are structurally related.

Indexed as

Sequence Homology, Nucleic AcidAnimalsCD4-Positive T-LymphocytesChromosome MappingChromosomesChromosomes, Human, Pair 2Crosses, GeneticGenetic LinkageHumansHybrid CellsHylobatesMetaphaseMiceMice, Inbred C57BLReceptors, VirusRetroviridaeReceptors, Virus

Identifiers

PMID1672162
PMCPMC239979

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.