首页> 美国卫生研究院文献>Journal of Virology >Human adenovirus type 9 E4 open reading frame 1 encodes a cytoplasmic transforming protein capable of increasing the oncogenicity of CREF cells.
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Human adenovirus type 9 E4 open reading frame 1 encodes a cytoplasmic transforming protein capable of increasing the oncogenicity of CREF cells.

机译:人类9型腺病毒E4开放阅读框1编码一种能够提高CREF细胞致癌性的胞质转化蛋白。

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摘要

The induction of estrogen-dependent rat mammary tumors by human adenovirus type 9 (Ad9) requires the Ad9 E4 open reading frame 1 (9ORF1) protein, which alone can transform that rat embryo fibroblast cell line CREF in vitro. In the present study, independent pools of both 9ORF1-expressing and control CREF cells were generated by selection with G418 and compared with respect to transformed properties. Indirect immunofluorescence analyses revealed that more than 99% of the cells that made up the 9ORF1-transfected pools expressed 9ORF1 protein and, together with confocal laser scanning microscopy, indicated that this E4 protein was located predominantly within the cytoplasm of cells. With regard to transformation, cells of the 9ORF1-expressing pools differed from those of control pools by forming foci, displaying morphological alterations, growing more efficiently in soft agar, and reaching higher saturation densities. Following injection into immunocompetent syngeneic rats, the 9ORF1-expressing pool cells exhibited greatly enhanced oncogenicity compared with control pool cells. These results show that 9ORF1 protein (i) localizes predominantly within the cytoplasm, (ii) confers multiple general transformed characteristics to CREF cells in vitro, and (iii) increases the tumorigenic properties of these cells in vivo.
机译:人类9型腺病毒(Ad9)诱导雌激素依赖性大鼠乳腺肿瘤需要Ad9 E4开放阅读框1(9ORF1)蛋白,仅此蛋白就可以在体外转化该大鼠胚胎成纤维细胞系CREF。在本研究中,通过G418的选择产生了9ORF1表达细胞和对照CREF细胞的独立库,并就转化后的特性进行了比较。间接免疫荧光分析表明,组成9ORF1转染池的细胞中有99%以上都表达9ORF1蛋白,并与共聚焦激光扫描显微镜一起显示该E4蛋白主要位于细胞的细胞质内。关于转化,表达9ORF1的库的细胞与对照库的细胞不同,其形成灶,显示形态变化,在软琼脂中更有效地生长并达到更高的饱和密度。注射到具有免疫能力的同系大鼠中后,表达9ORF1的池细胞与对照池细胞相比,其致癌性大大增强。这些结果表明9ORF1蛋白(i)主要定位在细胞质内,(ii)在体外赋予CREF细胞多种一般转化的特性,并且(iii)在体内增加了这些细胞的致瘤特性。

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