Onichtchouk D, Glinka A, Niehrs C
Division of Molecular Embryology, Deutsches Krebforschungszentrum, Heidelberg, Germany.
Development. 1998 Apr;125(8):1447-56. doi: 10.1242/dev.125.8.1447.
Xvent-1 and Xvent-2 are members of a novel homeobox subfamily that have been implicated in dorsoventral patterning in Xenopus mesoderm and are thought to function in BMP signalling. Here we investigate the requirement for Xvent function by employing two dominant-negative strategies. Loss of Xvent function dorsalizes ventral mesoderm, induces secondary embryonic axes and directly neuralizes ectoderm. We further find that (1) Xvents act as transcriptional repressors, (2) Xvents function in an additive fashion and (3) a surprising number of genes are able to rescue dominant-negative Xvent phenotypes including Bmp-4, Smad-1 and wild-type Xvents and Xhox3, but not Xwnt-8. The results show that Xvent-1 and Xvent-2 are essential for ventral mesoderm formation and for preventing neural differentiation. A model is suggested to explain how Bmp-4 positional information is converted into distinct cellular responses.
Xvent-1和Xvent-2是一个新的同源异型框亚家族的成员,它们与非洲爪蟾中胚层的背腹模式形成有关,并且被认为在骨形态发生蛋白(BMP)信号传导中发挥作用。在这里,我们通过采用两种显性负性策略来研究Xvent功能的必要性。Xvent功能的丧失会使腹侧中胚层背化,诱导次级胚胎轴,并直接使外胚层神经化。我们进一步发现:(1)Xvent作为转录抑制因子发挥作用;(2)Xvent以累加方式发挥作用;(3)数量惊人的基因能够挽救显性负性Xvent的表型,包括Bmp-4、Smad-1以及野生型Xvent和Xhox3,但不包括Xwnt-8。结果表明,Xvent-1和Xvent-2对于腹侧中胚层的形成以及防止神经分化至关重要。我们提出了一个模型来解释Bmp-4的位置信息是如何转化为不同的细胞反应的。