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Inactive complex formation between E. coli RNA polymerase and inhibitor protein purified from T7 phage infected cells

Abstract

THE “host shut-off” function of T7 phage has been thought to result from an inhibition of the host Escherichia coli RNA polymerase, which transcribes host RNA and T7 early mRNA, by an early T7 protein presumably the product of gene 0.7, or the “host shut-off” gene1–4. When T7 infection proceeds, early mRNA synthesis is shut off and the T7-specific RNA polymerase5, the product of an early gene of T7 (gene 1), transcribes late mRNA. Thus, “host shut-off” is another control factor involved in the early–late switch of T7 gene expression in addition to the switch of two RNA polymerases from the host to the phage-coded enzyme transcribing early mRNA and late mRNA, respectively, at different times of infection3.

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HESSELBACH, B., NAKADA, D. Inactive complex formation between E. coli RNA polymerase and inhibitor protein purified from T7 phage infected cells. Nature 258, 354–357 (1975). https://doi.org/10.1038/258354a0

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