Howard Hughes Medical Institute and Department of Biological Chemistry, University of California, Los Angeles, CA 90095-1662, USA.
Mech Dev. 2002 Dec;119 Suppl 1(Suppl 1):S179-84. doi: 10.1016/s0925-4773(03)00113-8.
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.
Dpp/BMP 信号通路在脊椎动物和无脊椎动物之间高度保守。最近,Conley 及其同事对果蝇横脉缺失-2(cv-2)突变的分子特征进行了描述,这为 Dpp/BMP 途径引入了一个新的调控步骤(Development 127(2000)3945)。CV-2 蛋白是分泌性的,含有五个富含半胱氨酸(CR)的结构域,类似于果蝇中的 BMP 拮抗剂短体节(Short gastrulation, Sog)和脊椎动物中的 Chordin (Chd)。果蝇中的突变表型表明,CV-2 是翅膀中横脉结构分化所必需的,而这些结构分化需要高水平的 Dpp。本文介绍了果蝇 cv-2 蛋白的小鼠和人类同源物。小鼠基因位于 9A3 号染色体上,而人类基因定位于 7p14 号染色体上。CV-2 在小鼠发育过程中动态表达,特别是在高 BMP 信号区域,如后原肠胚、尾芽腹侧和前脊椎软骨。我们的结论是,CV-2 是 Dpp/BMP 信号通路的一种进化上保守的细胞外调节因子。