Hsu I C, Yang W K, Tennant R W, Brown A
Proc Natl Acad Sci U S A. 1978 Mar;75(3):1451-5. doi: 10.1073/pnas.75.3.1451.
Whole-cell DNA preparations isolated from SC-1 cells chronically infected with N- or B-tropic murine leukemia viruses (MuLV) were tested for infectious activity in an Fv-1n (NIH-3T3) and two Fv-Ib (C57BL/6 and SV-A31) cell cultures. Efficiency of transfection for all DNAs was better in the NIH-3T3 cells than in C57BL/6 or SV-A31 cells; and an [N-tropic MuLV]SC-1 cell DNA preparation was slightly more infectious than a [B-tropic MuLV]SC-1 cell DNA preparation in all three cell cultures, regardless of their Fv-1 genotypes. Progeny viruses from the transfection showed N- or B-tropism corresponding to that of the parent viruses produced by the infected SC-1 cells that were used for the DNA preparation. DNA dose-response studies in NIH-3T3 cells revealed a one-hit mechanism for both the [B-tropic MuLV]SC-1 cell DNA and the [N-tropic MuLV]SC-1 cell DNA preparation. These results demonstrate that, in contrast to virion infection, transfection of N- and B-tropic MuLV with DNA preparations from chronically infected cells is not affected by the Fv-1 gene.
从长期感染N-或B-嗜性鼠白血病病毒(MuLV)的SC-1细胞中分离出的全细胞DNA制剂,在Fv-1n(NIH-3T3)和两种Fv-Ib(C57BL/6和SV-A31)细胞培养物中进行了感染活性测试。所有DNA在NIH-3T3细胞中的转染效率都比在C57BL/6或SV-A31细胞中更高;并且在所有三种细胞培养物中,无论其Fv-1基因型如何,[N-嗜性MuLV]SC-1细胞DNA制剂的传染性都略高于[B-嗜性MuLV]SC-1细胞DNA制剂。转染产生的子代病毒表现出与用于制备DNA的受感染SC-1细胞产生的亲本病毒相对应的N-或B-嗜性。在NIH-3T3细胞中进行的DNA剂量反应研究表明,[B-嗜性MuLV]SC-1细胞DNA制剂和[N-嗜性MuLV]SC-1细胞DNA制剂均存在单次打击机制。这些结果表明,与病毒粒子感染不同,用慢性感染细胞的DNA制剂转染N-和B-嗜性MuLV不受Fv-1基因的影响。