Cowan K, Tegtmeyer P, Anthony D D
Proc Natl Acad Sci U S A. 1973 Jul;70(7):1927-30. doi: 10.1073/pnas.70.7.1927.
RNA produced by the Simian Virus 40 (SV40) mutant tsA30 during lytic infection of kidney cells of African green monkeys was examined by RNA-DNA competition-hybridization. This mutant is temperature-sensitive in a function (gene A) that regulates synthesis of viral DNA. No detectable difference between mutant RNA synthesized at the permissive temperature (33 degrees ) and wild-type viral RNA was found. During continuous infection with the mutant at the restrictive temperature (41 degrees ) only early viral RNA was produced. When mutant DNA and late RNA synthesis were initiated at the permissive temperature, a shift to the restrictive temperature rapidly terminated synthesis of viral DNA but not that of late viral RNA. The data indicate that the function of gene A is required before synthesis of late viral RNA and that after initiation, the production of late RNA continues without further expression of gene A or concomittant viral DNA synthesis.
通过RNA-DNA竞争杂交法检测了猿猴病毒40(SV40)突变体tsA30在非洲绿猴肾细胞裂解感染期间产生的RNA。该突变体在调节病毒DNA合成的功能(基因A)上对温度敏感。在允许温度(33摄氏度)下合成的突变体RNA与野生型病毒RNA之间未发现可检测到的差异。在限制温度(41摄氏度)下用该突变体连续感染期间,仅产生早期病毒RNA。当在允许温度下启动突变体DNA和晚期RNA合成时,转移到限制温度会迅速终止病毒DNA的合成,但不会终止晚期病毒RNA的合成。数据表明,在晚期病毒RNA合成之前需要基因A的功能,并且在启动后,晚期RNA的产生会继续,而无需基因A的进一步表达或伴随的病毒DNA合成。