Taira M, Saint-Jeannet J P, Dawid I B
Laboratory of Molecular Genetics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Proc Natl Acad Sci U S A. 1997 Feb 4;94(3):895-900. doi: 10.1073/pnas.94.3.895.
Anteroposterior patterning of neural tissue is thought to be directed by the axial mesoderm which is functionally divided into head and trunk organizer. The LIM class homeobox gene Xlim-1 is expressed in the entire axial mesoderm, whereas the distinct transcription factor Xbra is expressed in the notochord but not in the prechordal mesoderm. mRNA injection experiments showed that Xenopus animal explants (caps) expressing an activated form of Xlim-1 (a LIM domain mutant named 3m) induce anterior neural markers whereas caps coexpressing Xlim-1/3m and Xbra induce posterior neural markers. These data indicate that, in terms of neural inducing ability, Xlim-1/3m-expressing caps correspond to the head organizer and Xlim-1/3m plus Xbra-coexpressing caps to the trunk organizer. Thus the expression domains of Xlim-1 and Xbra correlate with, and possibly define, the functional domains of the organizer. In animal caps Xlim-1/3m initiates expression of a neuralizing factor, chordin, whereas Xbra activates embryonic fibroblast growth factor (eFGF) expression, as reported previously; these factors could mediate the neural inducing and patterning effects that were observed. A dominant-negative FGF receptor (XFD) inhibits posteriorization by Xbra in a dose-dependent manner, supporting the suggestion that eFGF or a related factor has posteriorizing influence.
神经组织的前后模式形成被认为是由轴中胚层引导的,轴中胚层在功能上分为头部和躯干组织者。LIM类同源框基因Xlim-1在整个轴中胚层表达,而独特的转录因子Xbra在脊索中表达,但在前索中胚层中不表达。mRNA注射实验表明,表达活化形式的Xlim-1(一种名为3m的LIM结构域突变体)的非洲爪蟾动物外植体(帽)诱导前神经标记物,而共表达Xlim-1/3m和Xbra的帽诱导后神经标记物。这些数据表明,就神经诱导能力而言,表达Xlim-1/3m的帽相当于头部组织者,共表达Xlim-1/3m和Xbra的帽相当于躯干组织者。因此,Xlim-1和Xbra的表达域与组织者的功能域相关,并且可能定义了组织者的功能域。如先前报道的那样,在动物帽中,Xlim-1/3m启动神经化因子脊索蛋白的表达,而Xbra激活胚胎成纤维细胞生长因子(eFGF)的表达;这些因子可能介导了所观察到的神经诱导和模式形成效应。一种显性负性FGF受体(XFD)以剂量依赖的方式抑制Xbra引起的后化,支持了eFGF或相关因子具有后化影响的观点。