Vasiliev O L, Lukyanov S A, Belyavsky A V, Kazanskaya O V, Zaraisky A G
Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow.
Int J Dev Biol. 1997 Dec;41(6):877-82.
To understand the molecular mechanism underlying in the earliest steps of the embryonic ectoderm subdivision into epidermis and neuroectoderm, it would be important to isolate differentially expressed genes in presumptive neuroectoderm and epidermis at the gastrula stage, the period of the divergence of the two adjacent ectodermal compartments. Meanwhile, the most direct approach for such a task, i.e. subtractive enrichment of cDNA from neuroectodermal and epidermal explants with differentially expressed gene sequences, was difficult to realize because of the high number of explants needed for this technique. In the present paper we report a novel effective and quite simple method of cDNA subtractive enrichment, based on amplification of cDNA in vitro by polymerase chain reaction (PCR) and allowing to use a very small amount of initial cDNA samples. With this method we have cloned cDNA of a novel gene of Xenopus laevis, which was named XEP-1 for its specific expression in the presumptive epidermis starting from the midgastrula stage.
为了了解胚胎外胚层分化为表皮和神经外胚层的最早步骤背后的分子机制,在原肠胚阶段(即两个相邻外胚层隔室分化的时期),分离推定神经外胚层和表皮中差异表达的基因非常重要。同时,完成这项任务最直接的方法,即从神经外胚层和表皮外植体中减去富含差异表达基因序列的cDNA,由于该技术需要大量外植体而难以实现。在本文中,我们报道了一种新颖、有效且非常简单的cDNA消减富集方法,该方法基于通过聚合酶链反应(PCR)在体外扩增cDNA,并允许使用极少量的初始cDNA样本。通过这种方法,我们克隆了非洲爪蟾一个新基因的cDNA,由于其从原肠胚中期开始在推定表皮中特异性表达,故将其命名为XEP-1。