Newfeld S J, Chartoff E H, Graff J M, Melton D A, Gelbart W M
Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Development. 1996 Jul;122(7):2099-108. doi: 10.1242/dev.122.7.2099.
The proteins necessary for signal transduction in cells responding to ligands of the TGF-beta family are largely unknown. We have previously identified Mad (Mothers against dpp), a gene that interacts with the TGF-beta family member encoded by decapentaplegic (dpp) in Drosophila. Assay of Mad's role in the DPP-dependent events of embryonic midgut development demonstrates that Mad is required for any response of the visceral mesoderm or endoderm to DPP signals from the visceral mesoderm. Replacement of the normal DPP promoter with a heterologous (hsp70) promoter fails to restore DPP-dependent responses in Mad mutant midguts. Experiments utilizing Mad transgenes regulated by tissue-specific promoters show that MAD is required specifically in cells responding to DPP. Immunohistochemical studies localize MAD to the cytoplasm in all tissues examined. Experiments in Xenopus embryos demonstrate that Drosophila MAD can function in the signaling pathway of BMP-4, a vertebrate homolog of dpp. Based on these results, we propose that Mad is a highly conserved and essential element of the DPP signal transduction pathway.
在细胞对转化生长因子-β(TGF-β)家族配体作出反应时,信号转导所需的蛋白质很大程度上尚不清楚。我们之前已鉴定出Mad(对抗dpp的母体),这是一个与果蝇中由“截瘫”(dpp)编码的TGF-β家族成员相互作用的基因。对Mad在胚胎中肠发育的DPP依赖性事件中的作用进行检测表明,Mad是内脏中胚层或内胚层对来自内脏中胚层的DPP信号作出任何反应所必需的。用异源(hsp70)启动子替换正常的DPP启动子无法恢复Mad突变中肠的DPP依赖性反应。利用受组织特异性启动子调控的Mad转基因进行的实验表明,MAD在对DPP作出反应的细胞中是特异性必需的。免疫组织化学研究将MAD定位到所有检测组织的细胞质中。非洲爪蟾胚胎实验表明,果蝇MAD可在BMP-4(dpp的脊椎动物同源物)的信号通路中发挥作用。基于这些结果,我们提出Mad是DPP信号转导通路中一个高度保守且必不可少的元件。