Sun Zhihui, Jin Peng, Tian Tian, Gu Yi, Chen Ye-Guang, Meng Anming
State Key Laboratory of Biomembrane and Membrane Biotechnology, Department of Biological Sciences and Biotechnology, Tsinghua University, Beijing 100084, China.
Biochem Biophys Res Commun. 2006 Jun 30;345(2):694-703. doi: 10.1016/j.bbrc.2006.04.148. Epub 2006 May 4.
Activin, Nodal, and Vg1, members of the transforming growth factor beta (TGFbeta) superfamily, transduce signal through type I receptors ALK4 or ALK7 and play important roles in mesoderm induction and patterning during vertebrate embryogenesis. However, the timing and magnitude of the ALK4/ALK7-mediated maternal TGFbeta signals are not clear. SB-431542 is identified as an inhibitor of the ALK4/ALK5/ALK7-mediated TGFbeta signals and its specificity in vertebrate embryos has not been reported. We demonstrate that SB-431542 is able to specifically and reproducibly block the Smad2/3-mediated TGFbeta signals in zebrafish embryo. Embryos exposed to SB-431542 exhibit various defects phenocopying Nodal-deficient mutants. SB-431542 treatments starting at different cell cycles before the midblastula transition lead to different degrees of developmental defects in mesoderm induction and patterning, suggesting that maternal TGFbeta signals are activated right after fertilization and required for mesoderm formation and patterning.
激活素、Nodal和Vg1是转化生长因子β(TGFβ)超家族的成员,它们通过I型受体ALK4或ALK7转导信号,并在脊椎动物胚胎发育过程中的中胚层诱导和模式形成中发挥重要作用。然而,ALK4/ALK7介导的母体TGFβ信号的时间和强度尚不清楚。SB-431542被鉴定为ALK4/ALK5/ALK7介导的TGFβ信号的抑制剂,其在脊椎动物胚胎中的特异性尚未见报道。我们证明,SB-431542能够特异性且可重复地阻断斑马鱼胚胎中Smad2/3介导的TGFβ信号。暴露于SB-431542的胚胎表现出各种类似于Nodal缺陷突变体的缺陷。在中囊胚转换之前的不同细胞周期开始进行SB-431542处理会导致中胚层诱导和模式形成出现不同程度的发育缺陷,这表明母体TGFβ信号在受精后立即被激活,并且是中胚层形成和模式形成所必需的。