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PMID: 8124717 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

A novel member of the interferon receptor family complements functionality of the murine interferon gamma receptor in human cells.

Cell ·Vol. 76 ·No. 5 ·1994-03-11 ·Pages 803-10

Hemmi S, Böhni R, Stark G, Di Marco F, Aguet M

Abstract

Expression of the human interferon gamma receptor (IFN-gamma R) in mouse cells is not sufficient to confer biological responsiveness to human IFN-gamma and vice versa. An additional species-specific component is required for signal transduction. We identified this cofactor by expression cloning in simian COS cells stably transfected with the nonfunctional murine IFN-gamma R and a IFN-gamma-inducible reporter construct encoding the human Tac antigen (interleukin-2 receptor alpha chain, CD25). A cDNA clone was obtained that, upon stable transfection, rendered human HEp-2 cells expressing the murine IFN-gamma R fully responsive to murine IFN-gamma. This cDNA encodes a novel 332 amino acid type I transmembrane protein that belongs to the IFN receptor family and that we designate IFN-gamma R beta chain.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Chromosomes, Human, Pair 21 Cloning, Molecular DNA, Complementary/genetics Genes Genetic Complementation Test Humans Mice Molecular Sequence Data Receptors, Interferon/chemistry,genetics Sequence Alignment Sequence Homology, Amino Acid
Chemicals
DNA, Complementary Receptors, Interferon interferon gamma receptor
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hemmi S
Institute of Molecular Biology I, University of Zürich, Switzerland.
Böhni R
Stark G
Di Marco F
Aguet M
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1994-03-11
Pages
803-10
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Databases
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