Shemesh J, Rotem-Yehudar R, Ehrlich R
Department of Cell Research and Immunology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Israel.
J Virol. 1991 Oct;65(10):5544-8. doi: 10.1128/JVI.65.10.5544-5548.1991.
Transformation of rodent cells by human adenoviruses is a well-established model system for studying the expression, regulation, and function of class I antigens. In this report, we demonstrate that the highly oncogenic adenovirus type 12 operates at the transcriptional and posttranscriptional levels in regulating the activity of major histocompatibility complex class I genes and products in transformed cells. Adenovirus type 12 suppresses the cell surface expression of class I antigens in most cell lines. Nevertheless, in a number of cell lines suppression is the result of reduction in the amount of stable specific mRNA, while in another group of cell lines suppression involves interference with processing of a posttranscriptional product. The two mechanisms operate both for the endogenous H-2 genes and for a miniature swine class I transgene that is expressed in the cells.
人腺病毒对啮齿动物细胞的转化是用于研究I类抗原的表达、调控和功能的一个成熟的模型系统。在本报告中,我们证明了高致癌性的12型腺病毒在转录和转录后水平调控转化细胞中主要组织相容性复合体I类基因和产物的活性。12型腺病毒在大多数细胞系中抑制I类抗原的细胞表面表达。然而,在一些细胞系中,抑制是稳定的特异性mRNA量减少的结果,而在另一组细胞系中,抑制涉及对转录后产物加工的干扰。这两种机制对内源H-2基因和在细胞中表达的微型猪I类转基因均起作用。