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Ga14-gene-dependent alterations of embryo development and cell growth in primary culture of sea urchins

机译:Ga14基因依赖性海胆原代培养中胚胎发育和细胞生长的变化

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摘要

Primary cell cultures from sea urchins have a low proliferative level that prevents the establishment of long-term cultures. To increase expression levels of the genes regulating cell growth in sea urchins, and thus enhance cell growth, we used the transcriptional activator gene Gal4 found earlier in yeast. Sea urchin embryos were treated with plasmid DNA containing the Gal4 gene. Expression of the transgene was confirmed by reverse transcriptase polymerase chain reaction. When the fully functional gene was used, embryos effectively formed teratoma-like structures after 50 to 55 hours of cultivation. In contrast, the Gal4 gene, devoid of acidic activating regions, possessed little activity as a teratogen. The Gal4-treated cells in blastula-derived culture showed higher DNA synthesis and higher proliferative activity than control cells. We suggest that formation of the teratoma-like structures in embryos, activation of DNA synthesis, and significant increase of cell number in embryo-derived cell cultures could be attributed to Gal4 gene action.
机译:海胆的原代细胞培养物的增殖水平较低,因此无法建立长期培养物。为了增加调节海胆中细胞生长的基因的表达水平,从而增强细胞生长,我们使用了酵母中较早发现的转录激活基因Gal4。用含有Gal4基因的质粒DNA处理海胆胚胎。通过逆转录酶聚合酶链反应证实了转基因的表达。当使用全功能基因时,胚胎在培养50至55小时后有效地形成了畸胎瘤样结构。相反,没有酸性激活区的Gal4基因作为致畸剂几乎没有活性。囊胚来源培养物中经Gal4处理的细胞比对照细胞显示出更高的DNA合成和更高的增殖活性。我们认为,胚胎中畸胎瘤样结构的形成,DNA合成的激活以及胚胎衍生细胞培养物中细胞数量的显着增加可能归因于Gal4基因的作用。

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