Stavnezer E, Barkas A E, Brennan L A, Brodeur D, Li Y
J Virol. 1986 Mar;57(3):1073-83. doi: 10.1128/JVI.57.3.1073-1083.1986.
The Sloan-Kettering viruses (SKVs) are replication-defective retroviruses that transform avian cells in vitro. Each of the three SKV isolates is a mixture of viruses with genomes ranging in size from 4.1 to 8.9 kilobases (kb) with a predominant genome of 5.7 kb. Using a cDNA representing a sequence, v-ski, that is SKV specific and held in common by the multiple SKV genomes, we generated a restriction map of the 5.7-kb SKV genome and molecularly cloned a ski-containing fragment from SKV proviral DNA. Southern hybridization and sequence analysis showed that the cloned DNA fragment consisted of the 1.3-kb ski sequence embedded in the p19gag sequence and followed by the remaining 5' half of the gag gene and small portions of both the pol and env genes. A large deletion encompassing the 3' half of gag and the 5' 80% of pol was mapped to a position about 1 kb downstream from the 3' ski-gag junction. To determine whether the cloned ski sequence had transforming activity, the ski-containing fragment and a cloned Rous-associated virus 1 (RAV-1) genome were used to construct an analog of the 5.7-kb SKV genome, RAV-SKV. Cotransfection of chicken embryo cells with RAV-SKV and RAV-1 yielded foci of transformed cells whose morphology was identical to that induced by the natural SKVs. The transformed transfected cells produced transforming virus with a 5.7-kb ski-containing genome and synthesized a gag-containing polyprotein of 110 kilodaltons (kDa). Several nonproducer clones of RAV-SKV-transformed cells were analyzed, and most were found to synthesize a 5.7-kb SKV RNA and a 110-kDa polyprotein. One clone was found to contain an 8.9-kb SKV RNA, and this clone synthesized a 125-kDa polyprotein. Since both the 5.7- and 8.9-kb genomes and the 110- and 125-kDa polyproteins had been identified in studies on the natural SKVs, the present results not only demonstrate the transforming activity of these individual SKVs but also suggest mechanisms for their generation.
斯隆 - 凯特琳病毒(SKVs)是复制缺陷型逆转录病毒,可在体外转化禽类细胞。三种SKV分离株中的每一种都是病毒混合物,其基因组大小从4.1到8.9千碱基(kb)不等,主要基因组为5.7 kb。利用代表一种序列(v-ski)的cDNA,该序列是SKV特异的且为多个SKV基因组所共有,我们构建了5.7 kb SKV基因组的限制性图谱,并从SKV前病毒DNA中分子克隆了一个含ski的片段。Southern杂交和序列分析表明,克隆的DNA片段由嵌入p19gag序列中的1.3 kb ski序列组成,其后是gag基因剩余的5' 半段以及pol和env基因的小部分。一个包含gag 3' 半段和pol 5' 80% 的大缺失被定位到3' ski - gag连接处下游约1 kb的位置。为了确定克隆的ski序列是否具有转化活性,含ski的片段和克隆的劳氏相关病毒1(RAV - 1)基因组被用于构建5.7 kb SKV基因组的类似物RAV - SKV。用RAV - SKV和RAV - 1共转染鸡胚细胞产生了转化细胞灶,其形态与天然SKVs诱导的相同。转化的转染细胞产生了含5.7 kb ski基因组的转化病毒,并合成了110千道尔顿(kDa)的含gag多蛋白。对几个RAV - SKV转化细胞的非产生性克隆进行了分析,发现大多数克隆合成了5.7 kb的SKV RNA和110 kDa多蛋白。发现一个克隆含有8.9 kb的SKV RNA,该克隆合成了125 kDa多蛋白。由于在对天然SKVs的研究中已经鉴定出了5.7 kb和8.9 kb基因组以及110 kDa和125 kDa多蛋白,目前的结果不仅证明了这些单个SKVs的转化活性,还提示了它们产生的机制。