RETRACTED: Mouse Crossveinless-2 is the vertebrate homolog of a Drosophila extracellular regulator of BMP signaling (Retracted Article)

被引:35
作者
Coffinier, Catherine [1 ]
Ketpura, Nan [1 ]
Tran, Uyen [1 ]
Geissert, Douglas [1 ]
De Robertis, E. M. [1 ]
机构
[1] Univ Calif Los Angeles, Howard Hughes Med Inst, Dept Biol Chem, Los Angeles, CA 90095 USA
关键词
crossveinless-2; chordin; twisted gastrulation; short gastrulation; BMP; Dpp; tolloid; CR domain; von Willebrand factor type D domain; TIL domain; extracellular matrix; organogenesis; somite; sclerotome; notochord; neural crest; dorsal root ganglion; branchial arch; cartilage; vertebra; intervertebral disc; lung;
D O I
10.1016/S0925-4773(03)00113-8
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Dpp/BMP signaling pathway is highly conserved between vertebrates and invertebrates. The recent molecular characterization of the Drosophila crossveinless-2 (cv-2) mutation by Conley and colleagues introduced a novel regulatory step in the Dpp/BMP pathway ( Development 127 ( 2000) 3945). The CV-2 protein is secreted and contains five cysteine-rich (CR) domains similar to those observed in the BMP antagonist Short gastrulation (Sog) of Drosophila and Chordin (Chd) of vertebrates. The mutant phenotype in Drosophila suggests that CV-2 is required for the differentiation of crossvein structures in the wing which require high Dpp levels. Here we present the mouse and human homologs of the Drosophila cv-2 protein. The mouse gene is located on chromosome 9A3 while the human locus maps on chromosome 7p14. CV-2 is expressed dynamically during mouse development, in particular in regions of high BMP signaling such as the posterior primitive streak, ventral tail bud and prevertebral cartilages. We conclude that CV-2 is an evolutionarily conserved extracellular regulator of the Dpp/BMP signaling pathway. (c) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:S179 / S184
页数:6
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