Jolicoeur P, Baltimore D
Cell. 1976 Jan;7(1):33-9. doi: 10.1016/0092-8674(76)90252-x.
The production of virus and the synthesis of virus-specific RNA has been studied in Fv-1n/n (NIH/3T3, SIM) and Fv-1b/b (BALB/3T3, SIM-R) cell lines after infection with N- or B-tropic MuLV. It was found that virus production, measured by reverse transcriptase activity in the medium, was 70-100 fold lower in cells resistant at the Fv-1 locus than in permissive cells. The virus-specific RNA, detected by hybridization. In RNA excess with complementary DNA, was reduced by approximately 70-100 fold in cytoplasm of resistant cells compared to permissive cells. A reduction of the same magnitude was observed in the levels of virus-specific RNA extracted from nuclei of resistant cells. Our data therefore show that virus-specific RNA levels are reduced in cells nonpermissive at the Fv-1 locus, suggesting that restriction of the Fv-1 gene product occurs at the level of transcription of the viral genome or at a pre-integration step, or, alternatively, that the RNA transcripts are rapidly degraded after their synthesis.
在用 N-嗜性或 B-嗜性 MuLV 感染 Fv-1n/n(NIH/3T3,SIM)和 Fv-1b/b(BALB/3T3,SIM-R)细胞系后,对病毒产生及病毒特异性 RNA 的合成进行了研究。结果发现,通过培养基中的逆转录酶活性测定,Fv-1 位点抗性细胞中的病毒产生量比允许性细胞低 70 - 100 倍。通过与互补 DNA 在 RNA 过量情况下杂交检测到的病毒特异性 RNA,与允许性细胞相比,抗性细胞胞质中的病毒特异性 RNA 减少了约 70 - 100 倍。从抗性细胞核中提取的病毒特异性 RNA 水平也观察到了相同程度的降低。因此,我们的数据表明,Fv-1 位点非允许性细胞中的病毒特异性 RNA 水平降低,这表明 Fv-1 基因产物的限制发生在病毒基因组转录水平或整合前步骤,或者,RNA 转录本在合成后迅速降解。