Steinbeisser H, De Robertis E M, Ku M, Kessler D S, Melton D A
Molecular Biology Institute, University of California, Los Angeles 90024-1737.
Development. 1993 Jun;118(2):499-507. doi: 10.1242/dev.118.2.499.
In this study, we compare the effects of three mRNAs-goosecoid, activin and Xwnt-8- that are able to induce partial or complete secondary axes when injected into Xenopus embryos. Xwnt-8 injection produces complete secondary axes including head structures whereas activin and goosecoid injection produce partial secondary axes at high frequency that lack head structures anterior to the auditory vesicle and often lack notochord. Xwnt-8 can activate goosecoid only in the deep marginal zone, i.e., in the region in which this organizer-specific homeobox gene is normally expressed on the dorsal side. Activin B mRNA, however, can turn on goosecoid in all regions of the embryo. We also tested the capacity of these gene products to restore axis formation in embryos in which the cortical rotation was blocked by UV irradiation. Whereas Xwnt-8 gives complete rescue of anterior structures, both goosecoid and activin give partial rescue. Rescued axes including hindbrain structures up to level of the auditory vesicle can be obtained at high frequency even in the absence of notochord structures. The possible functions of Wnt-like and activin-like signals and of the goosecoid homeobox gene, and their order of action in the formation of Spemann's organizer are discussed.
在本研究中,我们比较了三种mRNA——鹅膏蕈氨酸、激活素和Xwnt-8——注入非洲爪蟾胚胎时诱导部分或完整次级轴的效果。注射Xwnt-8可产生包括头部结构的完整次级轴,而注射激活素和鹅膏蕈氨酸则高频产生缺乏听泡前方头部结构且常缺乏脊索的部分次级轴。Xwnt-8仅能在深层边缘区激活鹅膏蕈氨酸,即在背侧正常表达该组织者特异性同源盒基因的区域。然而,激活素B mRNA能在胚胎的所有区域开启鹅膏蕈氨酸的表达。我们还测试了这些基因产物恢复经紫外线照射阻断皮层旋转的胚胎中轴形成的能力。虽然Xwnt-8能完全挽救前部结构,但鹅膏蕈氨酸和激活素均只能部分挽救。即使没有脊索结构,也能高频获得包括直至听泡水平后脑结构的挽救轴。讨论了Wnt样和激活素样信号以及鹅膏蕈氨酸同源盒基因的可能功能,以及它们在斯佩曼组织者形成中的作用顺序。