Surin V L, Sats N V, Tagiev A F
Mol Biol (Mosk). 1994 Mar-Apr;28(2):350-4.
In this investigation the primary structure of E1A and E1B regions of SA7 (C8) simian adenovirus integrated in malignant SH2 rat cell line was studied. Southern blotting revealed at least two copies of the SA7 oncogene integrated in the SH2 genome. PCR analysis of E1A and E1B regions showed heteroduplex structures, proving the different structure of the integrated copies. The heteroduplex molecules with different electrophoretic mobility were separated, and chains corresponding to different copies were sequenced according to the modified Sanger method. We found that two copies differ mainly in microsatellite regions, in E1A between positions 894-902 (GCG)3/(GCG)4, in E1B between positions 2037-2048 (GCA)3/(GCA)4. It is necessary to stress that all deviations found belong to the coding regions of the SA7 oncogene.
在本研究中,对整合于恶性SH2大鼠细胞系中的SA7(C8)猿猴腺病毒的E1A和E1B区域的一级结构进行了研究。Southern印迹分析显示,SH2基因组中整合了至少两个拷贝的SA7癌基因。对E1A和E1B区域的PCR分析显示出异源双链结构,证明了整合拷贝的结构不同。分离出具有不同电泳迁移率的异源双链分子,并根据改良的桑格方法对对应于不同拷贝的链进行测序。我们发现,两个拷贝主要在微卫星区域存在差异,在E1A区域中位于894 - 902位之间,为(GCG)3/(GCG)4;在E1B区域中位于2037 - 2048位之间,为(GCA)3/(GCA)4。需要强调的是,所有发现的偏差均属于SA7癌基因的编码区域。