Eldon E D, Angerer L M, Angerer R C, Klein W H
Department of Biochemistry and Molecular Biology, University of Texas, M.D. Anderson Hospital and Tumor Institute, Houston 77030.
Genes Dev. 1987 Dec;1(10):1280-92. doi: 10.1101/gad.1.10.1280.
We have characterized the temporal and spatial expression of Spec3 mRNA in embryos of the sea urchin, Strongylocentrotus purpuratus. This mRNA, 2.0 kb in length, is present at low levels in unfertilized eggs but accumulates rapidly during cleavage, increasing 50-fold by hatching blastula stage. Message levels then decline abruptly, remain constant during mesenchyme blastula and gastrula stages, and increase again during prism and pluteus stages. This accumulation pattern is quite similar to that of the ectodermally expressed beta-tubulin mRNAs described recently by Harlow and Nemer (1987a). In situ hybridization shows that although Spec3 message accumulates in all blastomeres at early blastula stages, it later becomes restricted to ectoderm. By late blastula stage, hybridization is strongest in the animal hemisphere. At gastrula, signals are variable over ectoderm, and by pluteus, grains are concentrated in the ciliary band, though present in other ectodermal cells as well. Deciliation and regeneration of cilia in gastrula-stage embryos results in a four- to fivefold increase in Spec3 mRNA levels, implying that the Spec3 gene product is associated with ciliogenesis. Spec3 mRNA is encoded by a single gene in the haploid genome, and characterization of the gene shows that it contains three exons that encode an open reading frame for a hydrophobic protein of 21.6 kD. The reading frame reveals that the carboxy-terminal part of the protein contains two long hydrophobic stretches, 31 and 37 residues long, separated by short hydrophilic regions of six to eight residues. The presence of these two distinct hydrophobic stretches suggests that the Spec3 protein contains two alpha-helical domains that either span the lipid bilayer or are associated with some other hydrophobic environment.
我们已经对紫海胆胚胎中Spec3 mRNA的时空表达进行了表征。这种长度为2.0 kb的mRNA在未受精卵中含量较低,但在卵裂过程中迅速积累,到囊胚孵化阶段增加了50倍。随后信息水平急剧下降,在间充质囊胚和原肠胚阶段保持恒定,并在棱柱体和长腕幼虫阶段再次增加。这种积累模式与Harlow和Nemer(1987a)最近描述的外胚层表达的β-微管蛋白mRNA的积累模式非常相似。原位杂交显示,尽管Spec3信息在囊胚早期的所有卵裂球中积累,但后来仅限于外胚层。到囊胚后期,动物半球的杂交最强。在原肠胚阶段,外胚层的信号变化不定,到长腕幼虫阶段,颗粒集中在纤毛带,尽管在其他外胚层细胞中也有。原肠胚阶段胚胎的纤毛脱失和再生导致Spec3 mRNA水平增加四到五倍,这意味着Spec3基因产物与纤毛发生有关。Spec3 mRNA由单倍体基因组中的一个基因编码,该基因的表征表明它包含三个外显子,编码一个21.6 kD疏水蛋白的开放阅读框。阅读框显示该蛋白的羧基末端部分包含两个长疏水片段,分别为31和37个残基长,由六到八个残基的短亲水区域隔开。这两个不同疏水片段的存在表明Spec3蛋白包含两个α-螺旋结构域,它们要么跨越脂质双层,要么与其他一些疏水环境相关。