Cellular Responses to Sodium Butyrate Exhibit the Dominance of One Parental Phenotype in Somatic Cell Hybrids

G.Stanley Cox
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Abstract

The glycoprotein hormone α-subunit (GPHα) gene is inducible by sodium butyrate (NaBtr) in nontrophoblastic tumor cell lines such as HeLa (cervical carcinoma) but not in trophoblastic tumor cell lines such as JEG-3 (choriocarcinoma). The studies summarized in this report examined the ability of NaBtr to induce GPHα expression in somatic cell hybrids between HeLa SR3hyg and JEG-3neo. The hybrid cells, pooled clones resistant to both hygromycin B and G418 sulfate, have been named JELA and were indistinguishable from the SR3 parent with regard to induction of the GPHα gene. The effects of NaBtr on cell proliferation were also similar in HeLa and JELA but different from those in JEG-3. The GPHα gene could be induced by NaBtr in the JEG-3 parent only when they were simultaneously treated with cycloheximide (CHX). The ability of NaBtr to induce GPHα in CHX-treated JEG-3 cells occurred concomitantly with a change in the electrophoretic mobility of enhancer binding proteins as determined in gel shift assays. The DNA–protein complexes generated between a trophoblast specific element (TSE) and nuclear proteins in HeLa SR3 and JELA migrated significantly more slowly than the complex generated by JEG-3 nuclear proteins. However, when nuclear extracts were prepared from CHX-treated JEG-3 cells, the complex generated with the TSE oligonucleotide migrated more slowly than the complex from untreated JEG-3 cells and coincident with the complexes produced with nuclear extracts from HeLa SR3 and JELA cells. Together, these data demonstrate that inducibility of the GPHα gene by NaBtr in JELA cell hybrids resembles that of the HeLa SR3 parent and that its inducibility in the JEG-3 parent parallels the status of an enhancer binding protein (TSEB) as judged from changes in electrophoretic mobility. The results are consistent with a model in which the status of TSEB has a profound influence on the gene's response to NaBtr.

细胞对丁酸钠的反应在体细胞杂交中表现出一种亲本表型的优势
糖蛋白激素α-亚基(GPHα)基因在非滋养层肿瘤细胞系如HeLa(宫颈癌)中可被丁酸钠(NaBtr)诱导,而在滋养层肿瘤细胞系如JEG-3(绒毛膜癌)中不能被诱导。本研究总结了NaBtr在HeLa SR3hyg和JEG-3neo体细胞杂交中诱导GPHα表达的能力。杂交细胞是对潮霉素B和硫酸G418都有抗性的克隆,被命名为JELA,在诱导GPHα基因方面与SR3亲本没有区别。NaBtr对HeLa和JELA细胞增殖的影响相似,但与JEG-3不同。在JEG-3亲本中,NaBtr仅在与环己亚胺(CHX)同时处理时才能诱导GPHα基因。在chx处理的JEG-3细胞中,NaBtr诱导GPHα的能力与增强子结合蛋白的电泳迁移率的变化同时发生。在HeLa SR3和JELA中,滋养细胞特异性元件(TSE)与核蛋白之间产生的dna -蛋白复合物的迁移速度明显慢于JEG-3核蛋白产生的复合物。然而,从chx处理的JEG-3细胞中制备核提取物时,TSE寡核苷酸生成的复合物比未处理的JEG-3细胞的复合物迁移速度慢,并且与HeLa SR3和JELA细胞的核提取物产生的复合物一致。综上所述,这些数据表明,NaBtr在JELA细胞杂交中诱导GPHα基因的能力与HeLa SR3亲本相似,并且从电泳迁移率的变化判断,其在JEG-3亲本中的诱导能力与增强子结合蛋白(TSEB)的状态相似。该结果与一个模型一致,即TSEB的状态对该基因对NaBtr的反应有深远的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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