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首页> 外文期刊>Journal of Virology >Constitutive and retinoic acid-inducible expression of cytomegalovirus immediate-early genes in human teratocarcinoma cells.
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Constitutive and retinoic acid-inducible expression of cytomegalovirus immediate-early genes in human teratocarcinoma cells.

机译:人畸形瘤细胞中细胞病毒立即早期基因的组成型和视黄酸诱导表达。

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摘要

Human teratocarcinoma stem cells are nonpermissive for human cytomegalovirus (HCMV) but become permissive after being induced to differentiate by treatment with retinoic acid. We show that in uninduced teratocarcinoma stem cells, and also in transformed human 293 cells expressing adenovirus E1a gene products, the HCMV immediate-early (IE) 68,000-molecular-weight polypeptide (68K polypeptide) was not expressed, and consequently input viral genomes were not replicated. However, after differentiation of the teratocarcinoma cells, synthesis of the HCMV IE 68K polypeptide was induced, and viral DNA replication occurred. In contrast to our observations for HCMV, simian cytomegalovirus (SCMV) displayed constitutive expression of its analogous IE 94K polypeptide, and the input SCMV genomes were replicated in both uninduced stem cells and 293 cells. Since little, if any, HCMV IE RNA was detectable in human teratocarcinoma or 293 cells after infection under IE conditions, we suggest that a direct transcriptional block to permissivity occurs in these cells. The presence of tandemly repeated sequences which bind nuclear factor I protein in the promoter for the SCMV IE 94K polypeptide gene but not in the promoter for the HCMV IE 68K polypeptide gene may allow the expression of the simian but not of the human IE gene product in transformed cells.
机译:人类畸形瘤干细胞对于人巨细胞病毒(HCMV)是非诱导,但在诱导诱导以通过用视黄酸处理来分化后变得允许。我们表明,在不屈服的畸形瘤瘤干细胞中,并且在表达腺病毒E1A基因产物的转化后的人293细胞中,HCMV即时(即)68,000分子量多肽(68K多肽)未表达,因此输入病毒基因组没有复制。然而,在分化畸胎瘤细胞后,诱导HCMV IE 68K多肽的合成,并且发生病毒DNA复制。与我们对HCMV的观察结果相比,Simian CytomeGalovirus(SCMV)显示了其类似IE 94K多肽的组成型表达,并且在一个未被诱导的干细胞和293个细胞中复制了输入的SCMV基因组。由于在IE条件下感染后,如果在人类畸胎瘤或293个细胞中检测到少数,则在人类畸胎瘤或293个细胞中检测,我们表明这些细胞中发生直接转录嵌段。在SCMV的启动子中结合核因子I蛋白的串联反复序列的存在,但不在HCMV的启动子中,IE 68K多肽基因的启动子可以允许表达SIMIAN但不具有人IE基因产物转化细胞。

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