Twisted gastrulation can function as a BMP antagonist

被引:156
作者
Chang, CB
Holtzman, DA
Chau, S
Chickering, T
Woolf, EA
Holmgren, LM
Bodorova, J
Gearing, DP
Holmes, WE
Brivanlou, AH
机构
[1] Rockefeller Univ, Lab Vertebrate Mol Embryol, New York, NY 10021 USA
[2] Millennium Pharmaceut, Cambridge, MA 02139 USA
关键词
D O I
10.1038/35068583
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bone morphogenetic proteins (BMPs), including the fly homologue Decapentaplegic (DPP), are important regulators of early vertebrate and invertebrate dorsal-ventral development(1-6). An evolutionarily conserved BMP regulatory mechanism operates from fly to fish, frog and mouse to control the dorsal-ventral axis determination. Several secreted factors, including the BMP antagonist chordin/Short gastrulation (SOG)(7-12), modulate the activity of BMPs. In Drosophila, Twisted gastrulation (TSG) is also involved in dorsal-ventral patterning(13-15), yet the mechanism of its function is unclear. Here we report the characterization of the vertebrate Tsg homologues. We show that Tsg can block BMP function in Xenopus embryonic explants and inhibits several ventral markers in whole-frog embryos. Tsg binds directly to BMPs and forms a ternary complex with chordin and BMPs. Coexpression of Tsg with chordin leads to a more efficient inhibition of the BMP activity in ectodermal explants. Unlike other known BMP antagonists, however, Tsg also reduces several anterior markers at late developmental stages. Our data suggest that Tsg can function as a BMP inhibitor in Xenopus; furthermore, Tsg may have additional functions during frog embryogenesis.
引用
收藏
页码:483 / 487
页数:6
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