Chinsky J, Soeiro R
J Virol. 1982 Jul;43(1):182-90. doi: 10.1128/JVI.43.1.182-190.1982.
The murine gene Fv-1 exerts a major control over the replication of Friend murine leukemia virus (F-MuLV). An effect of the gene product has been determined to be at the level of accumulation and integration of viral DNA. Aphidicolin, an inhibitor of eucaryotic DNA polymerase alpha, was studied in murine cells infected either permissively or nonpermissively with regard to the Fv-1 genotype. Results indicated that inhibition of DNA polymerase alpha did not affect the accumulation of form III viral DNA in either permissive or nonpermissive cells. However, the normal accumulation of circular form I DNA in permissive cells was inhibited. The block in the accumulation of form I DNA resembled that occurring in some F-MuLV Fv-1-nonpermissive infections. Additionally, aphidicolin treatment resulted in the accumulation of novel low-molecular-weight viral DNA species, normally detectable in a nonpermissive infection of NIH cells with B-tropic F-MuLV. These data suggest that the Fv-1 gene product may interact with host DNA polymerase alpha to prevent viral replication.
小鼠基因Fv-1对Friend小鼠白血病病毒(F-MuLV)的复制起着主要控制作用。已确定该基因产物的作用是在病毒DNA的积累和整合水平上。真核DNA聚合酶α的抑制剂阿非迪霉素,在感染了Fv-1基因型的允许或非允许的小鼠细胞中进行了研究。结果表明,DNA聚合酶α的抑制在允许或非允许细胞中均不影响III型病毒DNA的积累。然而,允许细胞中环状I型DNA的正常积累受到抑制。I型DNA积累的阻断类似于在一些F-MuLV Fv-1非允许感染中发生的情况。此外,阿非迪霉素处理导致了新型低分子量病毒DNA种类的积累,这种积累通常在NIH细胞被B嗜性F-MuLV非允许感染时可检测到。这些数据表明,Fv-1基因产物可能与宿主DNA聚合酶α相互作用以阻止病毒复制。