Lindqvist B H
Proc Natl Acad Sci U S A. 1974 Jul;71(7):2752-5. doi: 10.1073/pnas.71.7.2752.
The DNA of helper-dependent coliphage P4 and the DNA of its helper-P2-show no detectable sequence homology as measured by DNA.DNA hybridization. The lack of cross-hybridization permits direct analysis of P4 as well as of P2 transcription in P4-infected P2 lysogens by RNA.DNA hybridization. P4-transactivated P2 transcription can be detected around 20 min after P4 infection of the P2 lysogen and the rate (per infected cell) of that transcription becomes equal to that of the P4 transcription at the end of the latent period of P4. Furthermore, P4 transcription appears to be stimulated by the presence of the helper. Conceivably, P2 codes for a stimulator of P4 transcription. Rifamycin has been used to investigate the role of the host RNA polymerase during P4 transactivation of P2 transcription. The results exclude the participation of a P4-coded RNA polymerase and indicate that the original host RNA polymerase is responsible for the bulk of P4 and P2 transcription during transactivation.
通过DNA-DNA杂交检测发现,辅助依赖型大肠杆菌噬菌体P4的DNA与其辅助噬菌体P2的DNA没有可检测到的序列同源性。缺乏交叉杂交使得通过RNA-DNA杂交能够直接分析P4感染的P2溶原菌中P4以及P2的转录情况。在P4感染P2溶原菌约20分钟后,可以检测到P4反式激活的P2转录,并且在P4潜伏期结束时,该转录(每个感染细胞)的速率与P4转录的速率相等。此外,P4转录似乎受到辅助噬菌体存在的刺激。可以想象,P2编码一种P4转录的刺激因子。利福平已被用于研究宿主RNA聚合酶在P4反式激活P2转录过程中的作用。结果排除了P4编码的RNA聚合酶的参与,并表明在反式激活过程中,最初的宿主RNA聚合酶负责大部分P4和P2的转录。