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

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.

[1]  J. Ravetch,et al.  Structure and expression of human IgG FcRII(CD32). Functional heterogeneity is encoded by the alternatively spliced products of multiple genes , 1989, The Journal of experimental medicine.

[2]  J. Kinet,et al.  Complete structure of the mouse mast cell receptor for IgE (Fc epsilon RI) and surface expression of chimeric receptors (rat-mouse-human) on transfected cells. , 1989, The Journal of biological chemistry.

[3]  G. Trinchieri,et al.  Murine natural killer cells express functional Fc gamma receptor II encoded by the Fc gamma R alpha gene , 1989, The Journal of experimental medicine.

[4]  B. Scallon,et al.  A human immunoglobulin G receptor exists in both polypeptide-anchored and phosphatidylinositol-glycan-anchored forms. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[5]  D. Schlessinger,et al.  Isolation of single-copy human genes from a library of yeast artificial chromosome clones. , 1989, Science.

[6]  J. Kinet Antibody-cell interactions: Fc receptors , 1989, Cell.

[7]  P. Leder,et al.  The gene for the rat mast cell high affinity IgE receptor alpha chain. Structure and alternative mRNA splicing patterns. , 1989, The Journal of biological chemistry.

[8]  G. Barsh,et al.  Human Fc gamma RIII: cloning, expression, and identification of the chromosomal locus of two Fc receptors for IgG. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[9]  B. Seed,et al.  Isolation and expression of functional high-affinity Fc receptor complementary DNAs. , 1989, Science.

[10]  J. Kinet,et al.  Receptors for Fc epsilon and Fc gamma are linked on mouse chromosome 1. , 1988, Journal of immunology.

[11]  T. Huizinga,et al.  The Pi-linked receptor FcRIII is released on stimulation of neutrophils , 1988, Nature.

[12]  T. Springer,et al.  The major Fc receptor in blood has a phosphatidylinositol anchor and is deficient in paroxysmal nocturnal haemoglobinuria , 1988, Nature.

[13]  B. Seed,et al.  The Fcγ receptor of natural killer cells is a phospholipid-linked membrane protein , 1988, Nature.

[14]  M. Hibbs,et al.  Molecular cloning of a human immunoglobulin G Fc receptor. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[15]  David,et al.  Isolation and expression of cDNA clones encoding a human receptor for IgG (Fc gamma RII) , 1987, The Journal of experimental medicine.

[16]  M. Olson,et al.  Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors. , 1987, Science.

[17]  D. Portnoy,et al.  Structural heterogeneity and functional domains of murine immunoglobulin G Fc receptors. , 1986, Science.

[18]  I. Mellman,et al.  A complementary DNA clone for a macrophage-lymphocyte Fc receptor , 1986, Nature.

[19]  M. Hibbs,et al.  The murine Fc receptor for immunoglobulin: purification, partial amino acid sequence, and isolation of cDNA clones. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[20]  J. Unkeless,et al.  Structure and function of human and murine receptors for IgG. , 1988, Annual review of immunology.

[21]  M. Seldin,et al.  Establishment of a molecular genetic map of distal mouse chromosome 1: further definition of a conserved linkage group syntenic with human chromosome 1q. , 1988, Genomics.