Joore J, Timmermans A, van de Water S, Folkers G E, van der Saag P T, Zivkovic D
Hubrecht Laboratory, The Netherlands Institute for Developmental Biology, Utrecht, The Netherlands.
Biochem Cell Biol. 1997;75(5):601-12.
Retinoid signalling plays an important role in embryonic pattern formation. Excess of retinoic acid during gastrulation results in axial defects in vertebrate embryos, suggesting that retinoids are involved in early anteroposterior patterning. To study retinoid signalling in zebrafish embryos, we developed a novel method to detect endogenous retinoids in situ in embryos, using a fusion protein of the ligand inducible transactivation domain of a retinoic acid receptor and a heterologous DNA binding domain. Using this method, we show that retinoid signalling is localized in zebrafish embryos in the region of the embryonic shield, and towards the end of gastrulation in a posterior dorsal domain. To investigate the relationships between the spatial distribution of retinoid signalling and the regulation of retinoid target genes, we studied the downregulation by retinoic acid of two genes expressed in anterior regions of the embryo, goosecoid and otx1. These experiments show that expression of both genes is strongly downregulated in the anterior neurectoderm of zebrafish embryos treated with retinoic acid, whereas mesendodermal expression is only mildly affected. Interestingly, a significant downregulation of goosecoid expression by retinoic acid was observed only during midgastrulation but not in earlier stages. In agreement with these results, spatial expression of goosecoid and otx1 does not overlap with the region of retinoid signalling in the late gastrula. Our data support the hypothesis that a localized retinoid signal is involved in axial patterning during early development, at least in part through the repression of anterior genes in posterior regions of the embryo. Furthermore, our data suggest that the action of retinoids is spatially as well as temporally regulated in the developing embryo.
视黄酸信号通路在胚胎模式形成中起着重要作用。原肠胚形成过程中视黄酸过量会导致脊椎动物胚胎出现轴向缺陷,这表明视黄酸参与了早期前后模式的形成。为了研究斑马鱼胚胎中的视黄酸信号通路,我们开发了一种新方法,利用视黄酸受体的配体诱导反式激活结构域与异源DNA结合结构域的融合蛋白,原位检测胚胎中的内源性视黄酸。使用这种方法,我们发现视黄酸信号通路在斑马鱼胚胎中定位于胚盾区域,并在原肠胚形成后期定位于后背部区域。为了研究视黄酸信号通路的空间分布与视黄酸靶基因调控之间的关系,我们研究了视黄酸对胚胎前部表达的两个基因——鹅膏菌素和otx1的下调作用。这些实验表明,在用视黄酸处理的斑马鱼胚胎的前神经外胚层中,这两个基因的表达均受到强烈下调,而中内胚层的表达仅受到轻微影响。有趣的是,仅在原肠胚中期观察到视黄酸对鹅膏菌素表达有显著下调,而在早期阶段则没有。与这些结果一致,在晚期原肠胚中,鹅膏菌素和otx1的空间表达与视黄酸信号通路的区域不重叠。我们的数据支持这样一种假设,即局部视黄酸信号在早期发育过程中参与轴向模式的形成,至少部分是通过抑制胚胎后部区域的前部基因来实现的。此外,我们的数据表明,视黄酸在发育中的胚胎中的作用在空间和时间上都是受到调控的。