Katz R A, Mitsialis S A, Guntaka R V
J Gen Virol. 1983 Feb;64 (Pt 2):429-35. doi: 10.1099/0022-1317-64-2-429.
The extent of methylation of several avian oncogenic proviruses was determined by using the restriction endonucleases HpaII and MspI. The results indicated that the transformation-defective proviruses (RAV-O or B77-td), which are exogenously introduced into avian host cells, were not methylated. However, endogenous proviruses (RAV-O) or ASV proviruses present in non-permissive host cells were found to be partly or completely methylated. The methyl-sensitive restriction endonuclease PvuI, which recognizes a unique site within the long terminal repeat in the ASV genome, failed to cleave proviruses present in several non-permissive host cells. From these results we suggest that modification of the sequence around the PvuI site results in reduced levels of transcription.
通过使用限制性内切酶HpaII和MspI来确定几种禽类致癌性前病毒的甲基化程度。结果表明,外源导入禽类宿主细胞的转化缺陷型前病毒(RAV - O或B77 - td)未发生甲基化。然而,发现非允许性宿主细胞中存在的内源性前病毒(RAV - O)或ASV前病毒部分或完全甲基化。甲基敏感的限制性内切酶PvuI可识别ASV基因组长末端重复序列内的一个独特位点,但未能切割几种非允许性宿主细胞中存在的前病毒。根据这些结果,我们认为PvuI位点周围序列的修饰会导致转录水平降低。