Durnam D M, Menninger J C, Chandler S H, Smith P P, McDougall J K
Program in Experimental Pathology, Fred Hutchinson Cancer Research Center, Seattle, Washington 98104.
Mol Cell Biol. 1988 May;8(5):1863-7. doi: 10.1128/mcb.8.5.1863-1867.1988.
Using in situ hybridization, we found that the U2 small nuclear RNA gene cluster mapped very close to and was frequently disrupted by the gaps and breaks induced specifically in the human 17q21-q22 region by highly oncogenic adenovirus type 12 (Ad12). Restriction mapping revealed no structural alterations in the U2 gene locus as a result of Ad12 infection. Likewise, no Ad12-induced alterations in U2 RNA levels were detected. We estimate that the maximum size of the region specifically disrupted by this virus was less than 350 to 700 kilobases. A comparison of these data with similar data regarding biochemically induced fragile sites was made.
通过原位杂交,我们发现U2小核RNA基因簇定位非常接近且经常被高致癌性12型腺病毒(Ad12)特异性诱导的人类17q21 - q22区域的间隙和断裂所破坏。限制性图谱分析显示,Ad12感染后U2基因位点没有结构改变。同样,未检测到Ad12诱导的U2 RNA水平变化。我们估计该病毒特异性破坏区域的最大大小小于350至700千碱基。并将这些数据与关于生化诱导的脆性位点的类似数据进行了比较。