Twu J S, Schloemer R H
Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis 46223.
J Virol. 1989 Jul;63(7):3065-71. doi: 10.1128/JVI.63.7.3065-3071.1989.
The manner by which the trans-acting factor encoded by the 1,828-base-pair (bp) BamHI DNA fragment of hepatitis B virus (HBV) suppresses the production of human beta interferon was determined. Steady-state levels of RNA specific for human beta interferon were decreased in cells that contained the 1,828-bp BamHI DNA fragment of HBV. The reduced accumulation of interferon-specific RNA was due to an inhibition of transcription of the interferon gene by the HBV trans-acting moiety. The expression of the interferon gene that is under the control of a heterologous promoter such as the simian virus 40 early promoter was not altered by the presence of the 1,828-bp BamHI HBV DNA fragment. In contrast, the HBV moiety inhibited the expression of the cat gene, whose expression is controlled by the regulatory DNA region of the human beta interferon gene. These results indicate that the HBV trans-acting moiety suppresses the expression of the human beta interferon gene at the transcriptional level by interacting with the regulatory DNA sequences 5' to the coding sequences for beta interferon.
已确定乙型肝炎病毒(HBV)1828碱基对(bp)的BamHI DNA片段编码的反式作用因子抑制人β干扰素产生的方式。在含有HBV 1828 bp BamHI DNA片段的细胞中,人β干扰素特异性RNA的稳态水平降低。干扰素特异性RNA积累减少是由于HBV反式作用部分对干扰素基因转录的抑制。由异源启动子如猿猴病毒40早期启动子控制的干扰素基因的表达不受1828 bp BamHI HBV DNA片段存在的影响。相反,HBV部分抑制了cat基因的表达,该基因的表达受人类β干扰素基因调控DNA区域的控制。这些结果表明,HBV反式作用部分通过与β干扰素编码序列5'端的调控DNA序列相互作用,在转录水平上抑制人β干扰素基因的表达。