Lepage T, Sardet C, Gache C
Unité de Biologie Cellulaire Marine, URA 671, Centre National de la Recherche Scientifique et Université de Paris VI, Villefranche-sur-Mer, France.
Dev Biol. 1992 Mar;150(1):23-32. doi: 10.1016/0012-1606(92)90004-z.
The sea urchin embryo at the blastula stage hatches from its protective fertilization envelope which is degraded by a secreted protease, the hatching enzyme. We have previously purified the hatching enzyme from Paracentrotus lividus (Lepage and Gache (1989). J. Biol. Chem. 264, 4787-4793), cloned its cDNA, and analyzed the temporal expression of its gene (Lepage and Gache (1990). EMBO J. 9, 3003-3012). We study here the temporal and spatial expression of the hatching enzyme gene in whole embryos by immunolabeling with an affinity-purified polyclonal antibody and by in situ hybridization using nonradioactive RNA probes. The timing of expression is consistent with our data on the activation of the gene, the mRNA accumulation in the blastula, and the role of the enzyme. Immunolabeling was observed only in blastula stage embryos; neither before the 128-cell stage nor after hatching. The distribution of the enzyme varies with time from a diffuse labeling around the nucleus to a punctate localization between the nucleus and the apical face of the blastomeres, and finally at the time of hatching, to a submembranous apical location. Not all the cells of an embryo are labeled. The presence of the hatching enzyme is restricted to a sharply delimited continuous territory spanning about two-thirds of the blastula. The orientation of this territory has been determined with respect to the animal-vegetal axis of the embryo using as a landmark the subequatorial pigmented band of the P. lividus species. The synthesis of the hatching enzyme only takes place in the animal-most two-thirds of the blastula. By in situ hybridization, the mRNA coding for the hatching enzyme is only detected in early blastulas, in a limited area having the same size and shape as the territory in which the protein is found. Thus the hatching enzyme gene is likely to be spatially controlled at the transcriptional level: its expression is restricted to a region of the blastula that corresponds roughly to the presumptive ectoderm territory. To date, the hatching enzyme gene products constitute the earliest molecular markers of the sea urchin embryo spatial organization along the primordial egg axis.
囊胚期的海胆胚胎会从其保护性的受精膜中孵化出来,受精膜会被一种分泌型蛋白酶——孵化酶降解。我们之前已从地中海海胆中纯化出孵化酶(勒佩奇和加什(1989年)。《生物化学杂志》264卷,4787 - 4793页),克隆了其cDNA,并分析了其基因的时序表达(勒佩奇和加什(1990年)。《欧洲分子生物学组织杂志》9卷,3003 - 3012页)。我们在此通过用亲和纯化的多克隆抗体进行免疫标记以及使用非放射性RNA探针进行原位杂交,研究整个胚胎中孵化酶基因的时空表达。表达的时间与我们关于该基因激活、囊胚中mRNA积累以及该酶作用的数据一致。免疫标记仅在囊胚期胚胎中观察到;在128细胞期之前或孵化之后均未观察到。该酶的分布随时间变化,从细胞核周围的弥散标记到细胞核与卵裂球顶面之间的点状定位,最终在孵化时,定位到膜下顶端位置。并非胚胎的所有细胞都被标记。孵化酶的存在局限于一个界限分明的连续区域,该区域跨越囊胚的约三分之二。利用地中海海胆物种的赤道下色素带作为地标,已确定该区域相对于胚胎动植物轴的方向。孵化酶的合成仅发生在囊胚最靠动物端的三分之二区域。通过原位杂交,编码孵化酶的mRNA仅在早期囊胚中被检测到,位于一个与发现该蛋白质的区域大小和形状相同的有限区域内。因此,孵化酶基因可能在转录水平受到空间控制:其表达局限于囊胚中大致对应预定外胚层区域的一个区域。迄今为止,孵化酶基因产物构成了海胆胚胎沿原始卵轴空间组织的最早分子标记。