Reuss F U, Coffin J M
Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
J Virol. 1998 Jul;72(7):6073-82. doi: 10.1128/JVI.72.7.6073-6082.1998.
Expression of mouse mammary tumor virus (MMTV)-encoded superantigens in B lymphocytes is required for viral transmission and pathogenesis. The mechanism of superantigen expression from the viral sag gene in B cells is largely unknown, due to problems with detection and quantification of these low-abundance proteins. We have established a sensitive superantigen-luciferase reporter assay to study the expression and regulation of the MMTV sag gene in B-cell lymphomas. The regulatory elements for retroviral gene expression are generally located in the 5' long terminal repeat (LTR) of the provirus. However, we found that neither promoters nor enhancers in the MMTV 5' LTR play a significant role in superantigen expression in these cells. Instead, the essential regulatory regions are located in the pol and env genes of MMTV. We report here that maximal sag expression in B-cell lines depends on an enhancer within the viral pol gene which can be localized to a minimal 183-bp region. Regulation of sag gene expression differs between B-cell lymphomas and pro-B cells, where an enhancer within the viral LTRs is involved. Thus, MMTV sag expression during B-cell development is achieved through the use of two separate enhancer elements.
小鼠乳腺肿瘤病毒(MMTV)编码的超抗原在B淋巴细胞中的表达是病毒传播和发病机制所必需的。由于检测和定量这些低丰度蛋白存在问题,B细胞中病毒sag基因超抗原表达的机制在很大程度上尚不清楚。我们建立了一种灵敏的超抗原-荧光素酶报告基因检测方法,以研究B细胞淋巴瘤中MMTV sag基因的表达和调控。逆转录病毒基因表达的调控元件通常位于前病毒的5'长末端重复序列(LTR)中。然而,我们发现MMTV 5' LTR中的启动子和增强子在这些细胞的超抗原表达中均未发挥重要作用。相反,关键的调控区域位于MMTV的pol和env基因中。我们在此报告,B细胞系中sag的最大表达取决于病毒pol基因内的一个增强子,该增强子可定位于一个最小的183碱基对区域。B细胞淋巴瘤和前B细胞中sag基因表达的调控有所不同,后者涉及病毒LTR内的一个增强子。因此,B细胞发育过程中的MMTV sag表达是通过使用两个独立的增强子元件实现的。