Cavin C, Buetti E
Swiss Institute for Experimental Cancer Research, Epalinges.
J Virol. 1995 Jun;69(6):3759-70. doi: 10.1128/JVI.69.6.3759-3770.1995.
Steroid hormones complexed with their receptors play an essential role in the regulation of mouse mammary tumor virus (MMTV) transcription. However, the need for additional tissue-specific regulatory factors is suggested by the lack of virus expression in liver, in which glucocorticoid receptors are highly abundant, and by the tissue-specific transcription of reporter genes linked to an MMTV long terminal repeat in transgenic mice. In this study, we characterized two distal-region regulatory elements, DRa and DRc, which, together with the distal glucocorticoid receptor binding site (DRb), increased transcription from the MMTV promoter in permissive cells. This was demonstrated by transfection of these sequences (DRa, DRb, and DRc) in different combinations with the natural MMTV promoter in mouse fibroblasts and mammary epithelial cells, followed by quantitative S1 nuclease mapping of the transcripts. We further showed by DNase I footprinting, methylation interference, and gel retardation assays with various nuclear extracts from permissive or nonpermissive tissues and cell lines that the factors binding to the DRa site are distinct and tissue-specific whereas those binding to DRc are ubiquitous.
与受体复合的类固醇激素在小鼠乳腺肿瘤病毒(MMTV)转录调控中起重要作用。然而,肝脏中缺乏病毒表达(其中糖皮质激素受体高度丰富)以及转基因小鼠中与MMTV长末端重复序列相连的报告基因的组织特异性转录表明,还需要其他组织特异性调节因子。在本研究中,我们鉴定了两个远端区域调节元件DRa和DRc,它们与远端糖皮质激素受体结合位点(DRb)一起,可增加允许细胞中MMTV启动子的转录。通过将这些序列(DRa、DRb和DRc)与天然MMTV启动子以不同组合转染到小鼠成纤维细胞和乳腺上皮细胞中,随后对转录本进行定量S1核酸酶作图,证明了这一点。我们通过DNase I足迹法、甲基化干扰以及用来自允许或非允许组织和细胞系的各种核提取物进行凝胶阻滞试验进一步表明,与DRa位点结合的因子是不同的且具有组织特异性,而与DRc结合的因子是普遍存在的。