Molecular cloning and characterization of mouse TIE and TEK receptor tyrosine kinase genes and their expression in hematopoietic stem cells

A Iwama, I Hamaguchi, M Hashiyama… - Biochemical and …, 1993 - Elsevier
A Iwama, I Hamaguchi, M Hashiyama, Y Murayama, K Yasunaga, T Suda
Biochemical and biophysical research communications, 1993Elsevier
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 …
Abstract
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.
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