TY - JOUR
T1 - 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
AU - Tagoh, Hiromi
AU - Kishi, Hiroyuki
AU - Muraguchi, Atsushi
N1 - Funding Information:
The authors thank Konomi Iwaki for her technical assistance and Miki Kiyohara for preparing the manuscript. This work was in part supported by grants-in-aid from the Ministry of Education, Science, Sports and Culture of Japan.
PY - 1996/4/25
Y1 - 1996/4/25
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=0029929017&partnerID=8YFLogxK
U2 - 10.1006/bbrc.1996.0667
DO - 10.1006/bbrc.1996.0667
M3 - 学術論文
C2 - 8630032
AN - SCOPUS:0029929017
SN - 0006-291X
VL - 221
SP - 744
EP - 749
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -