Molecular cloning and characterization of a novel stromal cell-derived cDNA encoding a protein that facilitates gene activation of recombination activating gene (RAG)-1 in human lymphoid progenitors

Biochem Biophys Res Commun. 1996 Apr 25;221(3):744-9. doi: 10.1006/bbrc.1996.0667.

Abstract

The activation and expression of recombination activation genes (RAGs) in lymphoid progenitors are regulated by signals from surface molecules of stromal cells and/or cytokines. Using a mRNA differential display method, we isolated a novel stromal cell-derived cDNA clone, C2.3, whose transcripts were intensively expressed in RAG-1-inducible stromal cell line, but rarely expressed in RAG-1-non inducible mutant cell line (PA6). The cDNA sequence had no homology to the known genes. The sequence revealed an open reading frame that encodes a 221 amino acid protein with 4 potential transmembrane domains, suggesting a possible role of C2.3 product as a membrane receptor. Introduction of C2.3 cDNA into PA6 mutant line restored the ability to activate RAG-1 gene in lymphoid progenitors, indicating that a C2.3 product may be involved in the induction of RAG-1 gene activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cell Line
  • Cloning, Molecular
  • DNA, Complementary
  • Gene Expression Regulation / physiology
  • Hematopoietic Stem Cells / metabolism*
  • Homeodomain Proteins*
  • Humans
  • Lymphocytes / metabolism*
  • Membrane Proteins / genetics*
  • Membrane Proteins / physiology
  • Mice
  • Molecular Sequence Data
  • Monosaccharide Transport Proteins
  • Proteins / genetics*
  • Transcriptional Activation*

Substances

  • DNA, Complementary
  • Homeodomain Proteins
  • Membrane Proteins
  • Monosaccharide Transport Proteins
  • Proteins
  • SLC50A1 protein, human
  • RAG-1 protein

Associated data

  • GENBANK/X96618