Evolutional imprints on the sequences of BMP2/4/DPP type proteins

被引:0
|
作者
Kunnapuu, Jaana [1 ]
Shimmi, Osamu [1 ]
机构
[1] Univ Helsinki, Inst Biotechnol, Helsinki, Finland
基金
芬兰科学院;
关键词
BMP2; BMP4; DPP; proprotein convertase; furin; DECAPENTAPLEGIC MORPHOGEN GRADIENT; PRODOMAIN; CLEAVAGE; EXPRESSION; SIGNAL; BMP-4;
D O I
暂无
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
Decapentaplegic (DPP) and bone morphogenetic protein (BMP)-2 and -4 type ligands form a branch of the transforming growth factor-beta (TGF beta) superfamily. They play prominent roles in metazoan developmental processes as diverse as cell proliferation, apoptosis, differentiation and cell-fate determination. Maturation of the BMP2/4/DPP type proteins requires proteolytic cleavage of their proproteins by furin-type proprotein convertases (PCs). Even though cleavage of the prodomain is critical for signaling, much less attention has been paid to the role of proteolytic processing. Our studies suggest that the cleavage sites of BMP2/4/DPP type proteins have been diversified and can be categorized into at least four different types. These findings indicate that the cleavage sites in BMP2/4/DPP prodomains are tolerant to mutations acquired through evolution and have adapted to diversified environments among species. These results provide insights for further studies of evolution and molecular diversity. In this Extra View we discuss the evolutional variation seen in the sequences of BMP2/4/DPP type proteins.
引用
收藏
页码:21 / 23
页数:3
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