Bone morphogenetic protein-3 family members and their biological functions

被引:32
|
作者
Hino, J
Kangawa, K
Matsuo, H
Nohno, T
Nishimatsu, S
机构
[1] Natl Cardiovasc Ctr, Res Inst, Dept Biochem, Osaka 5658565, Japan
[2] Kawasaki Med Sch, Dept Mol Biol, Okayama 7010192, Japan
来源
关键词
BMP-3; osteogenin; BMP-3b; GDF-10; TGF-beta; osteogenic activity; osteoblast; ALPase; dorsalizing activity; cerberus; head formation; neural inducer; precursor processing; embryos; review;
D O I
10.2741/1355
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
Bone morphogenetic protein-3 and 3b (BMP-3 and BMP-3b) together represent a unique subgroup of the BMP family. BMP-3b shares 82% amino acid identity with BMP-3 in the mature region (ligand domain), but only 37% in the pro-region (pro-domain). In osteoblasts, BMP-3 and 3b have similar antagonistic activity against BMP-2, but they are differentially regulated. In developing embryos, BMP-3 and 3b have different dorsalizing activities. BMP-3b triggers secondary head formation in an autonomous manner, whereas BMP-3 induces aberrant tail formation. Loss-of-function analysis demonstrates that coordinated activity of xBMP-3b and cerberus, a head inducer, are required for head formation in Xenopus embryos. At the molecular level, BMP-3b antagonizes both nodal-like proteins (Xnr1 and derriere) and ventralizing BMPs (BMP-2 and ADMP), whereas BMP-3 only antagonizes ventralizing BMPs. Moreover, BMP-3b, but not BMP-3, associates with the monomeric form of Xnr1, a nodal-like protein. These molecular features of BMP-3 and 3b are due to their distinct pro-regions. These findings suggest that the processing of precursor regions and assembly of BMP-3 and 3b are important in various developmental processes and organogenesis.
引用
收藏
页码:1520 / 1529
页数:10
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