IDENTIFICATION OF 2 BONE MORPHOGENETIC PROTEIN TYPE-I RECEPTORS IN DROSOPHILA AND EVIDENCE THAT BRK25D IS A DECAPENTAPLEGIC RECEPTOR

被引:235
作者
PENTON, A
CHEN, YJ
STAEHLINGHAMPTON, K
WRANA, JL
ATTISANO, L
SZIDONYA, J
CASSILL, JA
MASSAGUE, J
HOFFMANN, FM
机构
[1] UNIV WISCONSIN, SCH MED, GENET LAB, MADISON, WI 53706 USA
[2] MEM SLOAN KETTERING CANC CTR, HOWARD HUGHES MED INST, CELL BIOL & GENET PROGRAM, NEW YORK, NY 10021 USA
[3] UNIV HORT & FOOD IND, DEPT GENET & PLANT BREEDING, H-1518 BUDAPEST, HUNGARY
[4] UNIV TEXAS, DIV LIFE SCI, SAN ANTONIO, TX 78249 USA
关键词
D O I
10.1016/0092-8674(94)90294-1
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
Drosophila sequences at chromosomal positions 25D (Brk25D) and 43E (Brk43E) are similar to the TGF beta type I receptor serine/threonine kinases and are expressed broadly during embryogenesis. Brk25D binds dpp protein and bone morphogenetic protein 2 with high affinity. Mutations affecting Brk25D map to the gene thick veins and block the expression of two decapentaplegic-responsive (dpp-responsive) genes, dpp and labial, in the embryonic midgut. Defects in Brk25D receptor function combined with reduced expression of dpp ligand produce mutant phenotypes in the embryo and adult. Brk43E is the product of the gene saxophone, which also interacts with dpp. We conclude that dpp signaling in vivo is mediated by at least two receptors, Brk25D and Brk43E.
引用
收藏
页码:239 / 250
页数:12
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