Willer A, Saussele S, Gimbel W, Seifarth W, Kister P, Leib-Mösch C, Hehlmann R
III rd. Medizinische Klinik, Klinikum Mannheim, Universität Heidelberg, Germany.
Virus Genes. 1997;15(2):123-33. doi: 10.1023/a:1007910924177.
The human genome contains at least 50 copies of the human endogenous retrovirus K (HERV-K) family which is related to the mouse mammary tumor virus (MMTV). Some members have been shown to be transcriptionally active and to have large open reading frames. Using the RT-PCR method we have investigated the HERV-K env transcription pattern in several malignant tissues and in peripheral blood mononuclear cells PBMCs). Samples were derived from chronic myelogenous leukemia (CML), breast cancer, colon cancer, high and low grade non-Hodgkin's lymphomas, Hodgkin's disease, myelodysplastic syndrome, thyroid adenoma (TA) and from PBMCs of patients with breast cancer, gastric cancer, and of healthy individuals. We found abundant HERV-K env transcripts in all tissues under investigation. Using HERV-K 10 specific primers for amplification we detected in addition to transcripts with high homology to HERV-K 10 (ca. 96% homology on the amino acid level) also transcripts of low homology to HERV-K10 (ca. 71%). Interestingly, all solid tissues containing high percentages of malignant cells such as breast cancer, colon carcinoma, low and high grade non-Hodgkin's lymphomas showed exclusively HERV-K env related transcripts with low homology to HERV-K 10. In contrast, in samples containing only a low proportion of malignant cells or no malignant cells at all we observed both types of transcripts. Thus, our data suggest that the expression pattern of HERV-K elements in human cells is very heterogenous and subjected to a complex transcriptional regulation.
人类基因组包含至少50个拷贝的人类内源性逆转录病毒K(HERV-K)家族,该家族与小鼠乳腺肿瘤病毒(MMTV)相关。一些成员已被证明具有转录活性并拥有大的开放阅读框。我们使用逆转录聚合酶链反应(RT-PCR)方法研究了HERV-K env在几种恶性组织和外周血单个核细胞(PBMC)中的转录模式。样本来源于慢性粒细胞白血病(CML)、乳腺癌、结肠癌、高低级别非霍奇金淋巴瘤、霍奇金病、骨髓增生异常综合征、甲状腺腺瘤(TA),以及乳腺癌、胃癌患者和健康个体的PBMC。我们发现在所有被研究的组织中都有丰富的HERV-K env转录本。使用HERV-K 10特异性引物进行扩增,我们除了检测到与HERV-K 10具有高度同源性的转录本(氨基酸水平上约96%同源)外,还检测到与HERV-K10具有低同源性的转录本(约71%)。有趣的是,所有含有高比例恶性细胞的实体组织,如乳腺癌、结肠癌、高低级别非霍奇金淋巴瘤,仅显示出与HERV-K 10具有低同源性的HERV-K env相关转录本。相比之下,在仅含有低比例恶性细胞或根本没有恶性细胞的样本中,我们观察到了两种类型的转录本。因此,我们的数据表明,HERV-K元件在人类细胞中的表达模式非常异质,并受到复杂的转录调控。