Mouse lefty2 and zebrafish antivin are feedback inhibitors of nodal signaling during vertebrate gastrulation

被引:318
作者
Meno, C
Gritsman, K
Ohishi, S
Ohfuji, Y
Heckscher, E
Mochida, K
Shimono, A
Kondoh, H
Talbot, WS
Robertson, EJ
Schier, AF
Hamada, H [1 ]
机构
[1] NYU, Sch Med, Dept Cell Biol, Skirball Inst Biomol Med,Dev Genet Program, New York, NY 10016 USA
[2] Japan Sci & Technol Corp, CREST, Inst Mol & Cellular Biol, Div Mol Biol, Suita, Osaka, Japan
[3] Osaka Univ, Inst Mol & Cellular Biol, Div Dev Biol, Osaka 5650871, Japan
[4] Harvard Univ, Dept Mol & Cellular Biol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1097-2765(00)80331-7
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
Mammalian lefty and zebrafish antivin form a subgroup of the TGF beta superfamily. We report that mouse mutants for lefty2 have an expanded primitive! streak and form excess mesoderm, a phenotype opposite to that of mutants for the TGF beta gene nodal. Analogously, overexpression of Antivin or Lefty2 in zebrafish embryos blocks head and trunk mesoderm formation, a phenotype identical to that of mutants caused by loss of Nodal signaling. The lefty2 mutant phenotype is partially suppressed by heterozygosity for nodal. Similarly, the effects of Antivin and Lefty2 can be suppressed by overexpression of the nodal-related genes cyclops and squint or the extracellular domain of ActRIIB. Expression of antivin is dependent on Nodal signaling, revealing a feedback loop wherein Nodal signals induce their antagonists Lefty2 and Antivin to restrict Nodal signaling during gastrulation.
引用
收藏
页码:287 / 298
页数:12
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