Regulation of classical HLA class I genes in human choriocarcinoma cells by nuclear proteins binding to MHC class I regulatory elements

Am J Reprod Immunol. 1995 Nov;34(5):323-31. doi: 10.1111/j.1600-0897.1995.tb00959.x.

Abstract

Problem: The regulation of classical HLA class I genes in choriocarcinoma have been reported.

Methods: We determined whether four choriocarcinoma cell lines expressed classical HLA class I or HLA-G by a reverse transcription-polymerase chain reaction (RT-PCR) and studied the regulatory mechanism of classical class I using a gel mobility shift assay.

Results: NUC1 and SCH expressed classical class I but not HLA-G. GCH1 and Jar did neither. Nuclear protein binding to the class I regulatory element (CRE) was detected in NUC1 and SCH. Interferon-gamma augmented both classical class I expression and the DNA-protein complex in NUC1. The DNA-protein complex was not observed in GCH1, and Jar showed a CRE-binding protein with different electrophoretic mobility and binding affinity from that of SCH and NUC1.

Conclusion: The CRE is one of the regulatory elements of classical HLA class I genes in choriocarcinoma cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Choriocarcinoma / chemistry
  • Choriocarcinoma / genetics*
  • Choriocarcinoma / immunology
  • Female
  • Gene Expression Regulation, Neoplastic / immunology*
  • Genes, MHC Class I / immunology*
  • HLA Antigens / biosynthesis
  • HLA Antigens / genetics*
  • HLA Antigens / metabolism*
  • Histocompatibility Antigens Class I / biosynthesis
  • Histocompatibility Antigens Class I / genetics*
  • Histocompatibility Antigens Class I / metabolism*
  • Humans
  • Molecular Sequence Data
  • Nuclear Proteins / metabolism
  • Nuclear Proteins / pharmacology*
  • Pregnancy
  • Protein Binding / immunology
  • RNA, Messenger / biosynthesis
  • Regulatory Sequences, Nucleic Acid / immunology*
  • Tumor Cells, Cultured

Substances

  • HLA Antigens
  • Histocompatibility Antigens Class I
  • Nuclear Proteins
  • RNA, Messenger