Jüttermann R, Hosokawa K, Kochanek S, Doerfler W
Institute of Genetics, University of Cologne, Federal Republic of Germany.
J Virol. 1991 Apr;65(4):1735-42. doi: 10.1128/JVI.65.4.1735-1742.1991.
Sequence-specific methylation of the promoter and adjacent regions in mammalian genes transcribed by RNA polymerase II leads to the inhibition of these genes. So far, RNA polymerase III-transcribed genes have not been investigated in depth. We therefore studied methylation effects on the RNA polymerase III-transcribed VAI gene of adenovirus type 2 DNA. The VAI gene contains 20 5'-CG-3' dinucleotides, of which 4 (20%) can be methylated by HpaII (5'-CCGG-3') and HhaI (5'-GCGC-3'). Three of these 5'-CG-3' sequences are located close to the internal regulatory region of the VAI segment. An unmethylated, a 5'-CCGG-3'- and 5'-GCGC-3'-methylated, and a 5'-CG-3'-methylated pUC18 construct containing the VAI and VAII regions were transfected into mammalian cells. In many experiments, an inactivating effect of 5'-CCGG-3' and 5'-GCGC-3' DNA methylation on the VAI region was not observed. In contrast, methylation of all 20 5'-CG-3' sequences in the VAI region by a CpG-specific DNA methyltransferase from Spiroplasma species did interfere with VAI transcription. Transcription of the VAI- and VAII- and of the VAI-containing constructs was also shown to be inhibited in an in vitro cell-free transcription system after the constructs had been methylated at the 5'-CCGG-3' and 5'-GCGC-3' sequences or at all 5'-CG-3' sequences. When an oligodeoxyribonucleotide which carried the internal control block A of the VAI region was methylated at three 5'-CG-3' sequences, the formation of a complex with HeLa nuclear proteins was abrogated. The results presented support the notion that the VAI gene transcribed by the DNA-dependent RNA polymerase III is also inactivated by methylation of the decisive 5'-CG-3' sequences.
RNA聚合酶II转录的哺乳动物基因启动子及相邻区域的序列特异性甲基化会导致这些基因受到抑制。到目前为止,对于RNA聚合酶III转录的基因尚未进行深入研究。因此,我们研究了甲基化对2型腺病毒DNA中RNA聚合酶III转录的VAI基因的影响。VAI基因含有20个5'-CG-3'二核苷酸,其中4个(20%)可被HpaII(5'-CCGG-3')和HhaI(5'-GCGC-3')甲基化。这20个5'-CG-3'序列中的3个位于VAI片段的内部调控区域附近。将一个未甲基化的、一个经5'-CCGG-3'和5'-GCGC-3'甲基化的、以及一个经5'-CG-3'甲基化的包含VAI和VAII区域的pUC18构建体转染到哺乳动物细胞中。在许多实验中,未观察到5'-CCGG-3'和5'-GCGC-3' DNA甲基化对VAI区域有失活作用。相反,来自螺原体属的一种CpG特异性DNA甲基转移酶对VAI区域中所有20个5'-CG-3'序列进行甲基化确实会干扰VAI转录。在构建体在5'-CCGG-3'和5'-GCGC-3'序列或所有5'-CG-3'序列处甲基化后,在体外无细胞转录系统中也显示VAI、VAII以及含VAI的构建体的转录受到抑制。当一个携带VAI区域内部对照A的寡脱氧核糖核苷酸在3个5'-CG-3'序列处甲基化时,与HeLa核蛋白形成复合物的过程被消除。所呈现的结果支持这样一种观点:由DNA依赖性RNA聚合酶III转录的VAI基因也会因决定性的5'-CG-3'序列甲基化而失活。