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PMID: 2536956 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Isolation of a novel receptor cDNA establishes the existence of two PDGF receptor genes.

Science (New York, N.Y.) ·Vol. 243 ·No. 4892 ·1989-02-10 ·Pages 800-4

Matsui T, Heidaran M, Miki T, Popescu N, La Rochelle W, Kraus M, Pierce J, Aaronson S

Abstract

A genomic sequence and cloned complementary DNA has been identified for a novel receptor-like gene of the PDGF receptor/CSF1 receptor subfamily (platelet-derived growth factor receptor/colony-stimulating factor type 1 receptor). The gene recognized a 6.4-kilobase transcript that was coexpressed in normal human tissues with the 5.3-kilobase PDGF receptor messenger RNA. Introduction of complementary DNA of the novel gene into COS-1 cells led to expression of proteins that were specifically detected with antiserum directed against a predicted peptide. When the new gene was transfected into COS-1 cells, a characteristic pattern of binding of the PDGF isoforms was observed, which was different from the pattern observed with the known PDGF receptor. Tyrosine phosphorylation of the receptor in response to the PDGF isoforms was also different from the known receptor. The new PDGF receptor gene was localized to chromosome 4q11-4q12. The existence of genes encoding two PDGF receptors that interact in a distinct manner with three different PDGF isoforms likely confers considerable regulatory flexibility in the functional responses to PDGF.

MeSH Terms
Amino Acid Sequence Cells, Cultured Chromosomes, Human, Pair 4 Cloning, Molecular DNA/genetics Gene Expression Regulation Genes Humans Molecular Sequence Data Multigene Family Platelet-Derived Growth Factor/physiology Protein-Tyrosine Kinases/genetics RNA, Messenger/genetics Receptors, Cell Surface/genetics Receptors, Platelet-Derived Growth Factor Tissue Distribution
Chemicals
Platelet-Derived Growth Factor RNA, Messenger Receptors, Cell Surface DNA Protein-Tyrosine Kinases Receptors, Platelet-Derived Growth Factor
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Matsui T
Laboratory of Cellular and Molecular Biology, National Cancer Institute, Bethesda, MD 20892.
Heidaran M
Miki T
Popescu N
La Rochelle W
Kraus M
Pierce J
Aaronson S
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1989-02-10
Pages
800-4
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Databases
GENBANK
M21574
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