RESTRICTION INSENSITIVITY IN BACTERIOPHAGE-T5 .3. CHARACTERIZATION OF ECORI-SENSITIVE MUTANTS BY RESTRICTION ANALYSIS

Despite the fact that its DNA carries six EcoRI cleavage sites, bacteriophage T5 is able to grow on an EcoRI restricting host, suggesting that it specifies a restriction protection system. In the hope of identifying this protection system, mutants of T5 have been isolated which are unable to grow on an EcoRI restricting host. Analysis of the DNA of such mutants shows that they have each acquired two new EcoRI sites per molecule as a consequence of a single EcoRI site (ris) mutation located in the terminally repetitious, first step transfer (FST) region of the genome. The EcoRI sites generated by the ris mutations differ from the natural EcoRI sites in that the latter are situated on the second step transfer (SST) DNA, which suggests that the in vivo sensitivity of ris mutants is a consequence of having an EcoRI site on the FST DNA. This is understandable, if the hypothetical restriction protection genes are also located on the FST DNA. While expression of these genes would protect natural sites on the SST DNA, the ris sites would, on the contrary, enter an environment in which the protection, products had not yet been synthesized. Construction of double and triple ris mutants has allowed the ordering of the ris sites and the construction of an EcoRI restriction map of the FST region. In addition, the ris mutants allow estimation of the size of the terminal repetition of T5 DNA as 5.9 × 106 to 6.0 × 106 daltons. Correlation of the physical map of the FST region with the already established genetic map of this region allows orientation of the pre-early genes on the genetic and physical maps, and approximate localization of two amber mutations on the physical map. © 1979.