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PMID: 2139735 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Organization of the human and mouse low-affinity Fc gamma R genes: duplication and recombination.

Science (New York, N.Y.) ·Vol. 248 ·No. 4956 ·1990-05-11 ·Pages 732-5

Qiu WQ, de Bruin D, Brownstein BH, Pearse R, Ravetch JV

Abstract

Receptors for immunoglobulin G immune complexes (Fc gamma RII and Fc gamma RIII) are expressed on most hematopoietic cells and show much structural and functional diversity. In order to determine the genetic basis for this diversity, a family of genes encoding the human and mouse receptors was isolated and characterized. Humans have five distinct genes for low-affinity Fc gamma Rs, in contrast to two in the mouse. With the use of yeast artificial chromosomes, the genes encoding the human receptors were oriented and linked, which established the structure of this complex locus. Comparison of the human and mouse genes generated a model for the evolutionary amplification of this locus.

MeSH Terms
Animals Antigens, Differentiation/genetics,metabolism Base Sequence Blotting, Southern Exons Genome, Human Humans Immunoglobulin G/metabolism Introns Mice Molecular Sequence Data Multigene Family Mutation Receptors, Fc/genetics,metabolism Receptors, IgG Recombination, Genetic Restriction Mapping Spleen/immunology
Chemicals
Antigens, Differentiation Immunoglobulin G Receptors, Fc Receptors, IgG
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Qiu W Q
Division of Molecular Biology, Sloan-Kettering Institute, New York, NY 10021.
de Bruin D
Brownstein B H
Pearse R
Ravetch J V
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1990-05-11
Pages
732-5
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIGMS NIH HHS · GM 36306 · United States
NIGMS NIH HHS · GM 39256 · United States
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