Xu R H, Dong Z, Maeno M, Kim J, Suzuki A, Ueno N, Sredni D, Colburn N H, Kung H F
Laboratory of Biochemical Physiology, National Cancer Institute-Frederick Cancer Research and Development Center, MD 21702-1201, USA.
Proc Natl Acad Sci U S A. 1996 Jan 23;93(2):834-8. doi: 10.1073/pnas.93.2.834.
Previously, we elucidated the role of bone morphogenetic protein 4 (BMP-4) in the dorsal-ventral patterning of the Xenopus embryo by using a dominant negative mutant of the BMP-4 receptor (DN-BR). The present paper describes the involvement of Ras, Raf, and activator protein 1 (AP-1) in BMP-4 signaling during Xenopus embryonic development. The AP-1 activity was determined by injecting an AP-1-dependent luciferase reporter gene into two-cell-stage Xenopus embryos and measuring the luciferase activity at various developmental stages. We found that injection of BMP-4 mRNA increased AP-1 activity, whereas injection of DN-BR mRNA inhibited AP-1 activity. Similar inhibitory effects were seen with injection of mRNAs encoding dominant negative mutants of c-Ha-Ras, c-Raf, or c-Jun. These results suggest that the endogenous AP-1 activity is regulated by BMP-4/Ras/Raf/Jun signals. We next investigated the effects of Ras/Raf/AP-1 signals on the biological functions of BMP-4. DN-BR-induced dorsalization of the embryo, revealed by the formation of a secondary body axis or dorsalization of the ventral mesoderm explant analyzed by histological and molecular criteria, was significantly reversed by coinjection of [Val12]Ha-Ras, c-Raf, or c-Jun mRNA. Furthermore, the BMP-4-stimulated erythroid differentiation in the ventral mesoderm was substantially inhibited by coinjection with the dominant negative c-Ha-Ras, c-Raf, or c-Jun mutant. Our results suggest the involvement of Ras/Raf/AP-1 in the BMP-4 signaling pathway.
此前,我们通过使用骨形态发生蛋白4(BMP - 4)受体的显性负性突变体(DN - BR)阐明了BMP - 4在非洲爪蟾胚胎背腹模式形成中的作用。本文描述了Ras、Raf和激活蛋白1(AP - 1)在非洲爪蟾胚胎发育过程中参与BMP - 4信号传导的情况。通过将一个依赖AP - 1的荧光素酶报告基因注射到两细胞期的非洲爪蟾胚胎中,并在不同发育阶段测量荧光素酶活性来确定AP - 1活性。我们发现注射BMP - 4 mRNA可增加AP - 1活性,而注射DN - BR mRNA则抑制AP - 1活性。注射编码c - Ha - Ras、c - Raf或c - Jun显性负性突变体的mRNA也观察到类似的抑制作用。这些结果表明内源性AP - 1活性受BMP - 4/Ras/Raf/Jun信号调控。接下来,我们研究了Ras/Raf/AP - 1信号对BMP - 4生物学功能的影响。通过形成次生体轴或根据组织学和分子标准分析腹侧中胚层外植体的背化来揭示,DN - BR诱导的胚胎背化可被共注射[Val12]Ha - Ras、c - Raf或c - Jun mRNA显著逆转。此外,与显性负性c - Ha - Ras、c - Raf或c - Jun突变体共注射可显著抑制BMP - 4刺激的腹侧中胚层红细胞分化。我们的结果表明Ras/Raf/AP - 1参与了BMP - 4信号通路。