MAST-CELL GROWTH-FACTOR MAPS NEAR THE STEEL LOCUS ON MOUSE CHROMOSOME-10 AND IS DELETED IN A NUMBER OF STEEL ALLELES

被引:601
作者
COPELAND, NG
GILBERT, DJ
CHO, BC
DONOVAN, PJ
JENKINS, NA
COSMAN, D
ANDERSON, D
LYMAN, SD
WILLIAMS, DE
机构
[1] IMMUNEX CORP,DEPT EXPTL HEMATOL,SEATTLE,WA 98101
[2] IMMUNEX CORP,DEPT MOLEC BIOL,SEATTLE,WA 98101
关键词
D O I
10.1016/0092-8674(90)90298-S
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many spontaneous, chemical-induced, and radiation-induced dominant white spotting (W) and steel (SI) mutations have been identified in the mouse. W and SI mutations have similar phenotypic effects including deficiencies in pigment cells, germ cells, and blood cells. Numerous studies have suggested that W acts within the affected cell while SI instead exerts its effects in the extracellular environment. Recent findings demonstrating that W encodes the c-kit proto-oncogene, a tyrosine kinase membrane receptor, have suggested that SI encodes a ligand for c-kit. In the accompanying article we report the identification and purification of mast cell growth factor (MGF), a c-kit ligand. Here we describe the cloning of sequences encoding MGF. Furthermore, we show that Mgf maps near SI in the distal region of mouse chromosome 10 and is deleted in a number of SI alleles. These findings strongly support the notion that SI encodes the mast cell growth factor. © 1990.
引用
收藏
页码:175 / 183
页数:9
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