Structural analysis of the human interferon gamma receptor: a small segment of the intracellular domain is specifically required for class I major histocompatibility complex antigen induction and antiviral activity

Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11317-21. doi: 10.1073/pnas.89.23.11317.

Abstract

Mutations of the human interferon gamma (IFN-gamma) receptor intracellular domain have permitted us to define a restricted region of that domain as necessary for both induction of class I major histocompatibility complex antigen by IFN-gamma and protection against encephalomyocarditis virus. This region consists of five amino acids (YDKPH), all of which are conserved in the human and murine receptors. Tyr-457 and His-461 are essential for activity. Approximately 80% of the amino acids of the intracellular domain of the receptor is not required for major histocompatibility complex class I antigen induction or for antiviral protection against encephalomyocarditis virus. The observation that there was no protection by IFN-gamma against vesiculostomatitis virus indicates that other factors, in addition to chromosome 21 accessory factor(s), are required to generate the full complement of transduction signals from the human IFN-gamma receptor.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • CHO Cells
  • Cricetinae
  • Cytoplasm
  • DNA Mutational Analysis
  • Histocompatibility Antigens Class I / metabolism*
  • Humans
  • Interferon gamma Receptor
  • Interferon-gamma / metabolism*
  • Molecular Sequence Data
  • Receptors, Interferon / chemistry*
  • Receptors, Interferon / physiology
  • Recombinant Proteins / metabolism
  • Structure-Activity Relationship
  • Transfection
  • Viral Interference*

Substances

  • Histocompatibility Antigens Class I
  • Receptors, Interferon
  • Recombinant Proteins
  • Interferon-gamma