TY - JOUR
T1 - Molecular cloning and characterization of mouse TIE and TEK receptor tyrosine kinase genes and their expression in hematopoietic stem cells
AU - Iwama, Atsushi
AU - Hamaguchi, Isao
AU - Hashiyama, Motohiro
AU - Murayama, Yuko
AU - Yasunaga, Kunio
AU - Suda, Toshio
PY - 1993/8/31
Y1 - 1993/8/31
N2 - To identify receptor tyrosine kinases (RTKs) critical to early hematopoiesis, we performed polymerase chain reaction-based cloning from yolk sac and highly enriched bone marrow hematopoietic stem cells (HSCs). Characterization of two novel genes of their full-length cDNA sequences revealed that they were mouse homologues of the endothelial cell RTK genes, TIE and TEK. They shared a unique structural property of coexistent immunoglobulin-like domain, epidermal growth factor-like repeats, and fibronectin type III repeats in their extracellular domains. Both genes were expressed in a similar fashion in adult tissues and primitive hematopoietic cells, predominantly in the bone marrow HSCs.
AB - To identify receptor tyrosine kinases (RTKs) critical to early hematopoiesis, we performed polymerase chain reaction-based cloning from yolk sac and highly enriched bone marrow hematopoietic stem cells (HSCs). Characterization of two novel genes of their full-length cDNA sequences revealed that they were mouse homologues of the endothelial cell RTK genes, TIE and TEK. They shared a unique structural property of coexistent immunoglobulin-like domain, epidermal growth factor-like repeats, and fibronectin type III repeats in their extracellular domains. Both genes were expressed in a similar fashion in adult tissues and primitive hematopoietic cells, predominantly in the bone marrow HSCs.
UR - http://www.scopus.com/inward/record.url?scp=0027326213&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0027326213&partnerID=8YFLogxK
U2 - 10.1006/bbrc.1993.2045
DO - 10.1006/bbrc.1993.2045
M3 - Article
C2 - 8395828
AN - SCOPUS:0027326213
SN - 0006-291X
VL - 195
SP - 301
EP - 309
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 1
ER -