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2,3,7,8-四氯二苯并-对-二恶英的差异显示分析鉴定出Ras相关核蛋白结合蛋白2(RanBP2)基因的诱导。

Differential Display Analysis of 2,3,7,8-Tetrachlorodibenzo--dioxin Identified Induction of Ras-related Nuclear Protein Binding Protein2 (RanBP2) Gene.

作者信息

Kim Donghak, Lim Young-Ran, Park Hyoung-Goo, Kim Beom Joon, Chun Young-Jin

机构信息

16Department of Biological Sciences, Konkuk University, Seoul, 143-701 Korea.

Department of Dermatology, College of Medicine, Korea.

出版信息

Toxicol Res. 2009 Mar;25(1):35-40. doi: 10.5487/TR.2009.25.1.035. Epub 2009 Mar 1.

Abstract

TCDD (2,3,7,8-tetrachlorodibenzo--dioxin) and related halogenated aromatic hydrocarbons elicit a diverse spectrum of biochemical and toxic responses in laboratory animals and mammalian cells in culture. Toxicity and carcinogenicity of TCDD is well established but the molecular mechanism is still poorly understood. Here, we found the noble responsive genes to TCDD using the differential display analysis. Treatment of HepG2 cells with TCDD showed a significantly different mRNA expression pattern from the untreated cells in differential display analysis. The differentially displayed bands were isolated and used as probes in dot blot and Northern blot analyses. Of thirty-five isolated differentially displayed bands, only two bands were confirmed as positive in dot blot and Northern blot analyses. The nucleotides sequences of these clones were analyzed and the search of Genebank database revealed that one clone is highly homologous with RanBP2 (Ras-related nuclear protein binding protein2; 92%) and the other is an unknown gene. RanBP2 is a nucleoporin with SUMO E3 ligase activity that functions in both nucleocytoplasmic transport and mitosis and its role as a novel tumor suppressor has been recently proposed. Thus, these results may suggest the clue elucidating the toxic mechanism of TCDD through RanBP2.

摘要

2,3,7,8-四氯二苯并对二恶英(TCDD)及相关卤代芳烃在实验动物和培养的哺乳动物细胞中引发了多种生物化学和毒性反应。TCDD的毒性和致癌性已得到充分证实,但其分子机制仍知之甚少。在此,我们利用差异显示分析法找到了对TCDD有反应的基因。在差异显示分析中,用TCDD处理HepG2细胞后,其mRNA表达模式与未处理细胞有显著差异。分离出差异显示的条带,并将其用作点杂交和Northern杂交分析的探针。在分离出的35条差异显示条带中,只有两条在点杂交和Northern杂交分析中被确认为阳性。对这些克隆的核苷酸序列进行了分析,通过搜索基因库数据库发现,一个克隆与RanBP2(Ras相关核蛋白结合蛋白2;92%)高度同源,另一个是未知基因。RanBP2是一种具有SUMO E3连接酶活性的核孔蛋白,在核质运输和有丝分裂中均起作用,最近有人提出它作为一种新型肿瘤抑制因子的作用。因此,这些结果可能为通过RanBP2阐明TCDD的毒性机制提供线索。

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