Meijer I, Boot A J, Mahabir G, Zantema A, van der Eb A J
Laboratory for Molecular Carcinogenesis, Sylvius Laboratory, University of Leiden, The Netherlands.
Cell Immunol. 1992 Nov;145(1):56-65. doi: 10.1016/0008-8749(92)90312-d.
The early region 1 (E1) of human adenovirus (Ad) type 12 represses the expression of major histocompatibility (MHC) Class I genes in transformed primary rodent cells. In this paper we show that both NF-kappa B and KBF1 (p50 dimer) binding activity to the H2TF1 element in the Class I promoter is reduced in Ad12-13S-E1A-transformed cells compared to Ad5E1- or Ad12-12S-E1A-transformed cells. Consistently, in Ad12E1A-13S-transformed cells the H2TF1 element does not contribute to transcriptional activity in transient expression assays, whereas it does contribute in Ad12E1A-12S-transformed cells. Therefore, the most likely explanation is that reduced binding of NF-kappa B and KBF1 to the H2TF1 element accounts for the down-regulation of MHC Class I expression in Ad12E1- and Ad12E1A-13S-transformed cells.
12型人腺病毒(Ad)的早期区域1(E1)可抑制原代啮齿动物细胞转化过程中主要组织相容性(MHC)I类基因的表达。在本文中,我们发现,与Ad5 E1或Ad12 - 12S - E1A转化细胞相比,Ad12 - 13S - E1A转化细胞中NF-κB和KBF1(p50二聚体)与I类启动子中H2TF1元件的结合活性降低。同样,在Ad12 E1A - 13S转化细胞中,H2TF1元件在瞬时表达试验中对转录活性没有贡献,而在Ad12 E1A - 12S转化细胞中则有贡献。因此,最可能的解释是,NF-κB和KBF1与H2TF1元件的结合减少导致了Ad12 E1和Ad12 E1A - 13S转化细胞中MHC I类表达的下调。