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J Virol. 1974 February; 13(2): 378-385
Copyright © 1974 American Society for Microbiology. All Rights Reserved.
1 Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111
ABSTRACT
The inability of T7 to develop in cells of Escherichia coli containing F+ or substituted F' episomes is a result of the failure to synthesize late proteins; no in vivo translation of mRNA species synthesized by the T7 RNA polymerase occurs. Further experiments have been performed to measure the amount of late mRNA in T7-infected F'(PIF+) cells. (We have designated the property of phage inhibition of F factors as PIF; the wild-type episome is therefore F'[PIF+].) T7 late proteins were synthesized in vitro by using a system programed with RNA extracted from T7-infected F and F'(PIF+) cells. The T7 lysozyme, product of gene 3.5, and the gene 10 head protein were assayed. The following results were obtained: (i) mRNA capable of supporting in vitro synthesis of lysozyme and the gene 10 head protein is present in T7-infected F'(PIF+) cells; (ii) lysozyme mRNA extracted from T7-infected F'(PIF+) cells is present at 70 to 75% of the level found in T7-infected F cells; (iii) gene 10 mRNA is present at 35 to 78% of the level found in T7-infected F cells. No in vivo synthesis of either lysozyme or gene 10 protein can be detected in T7-infected F'(PIF+) cells although normal synthesis of these proteins occurs in F cells. These findings confirm that the block in T7 development in F'(PIF+) cells results from the failure to translate late classes of T7 RNA.
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