EcoRI analysis of bacteriophage P22 DNA packaging.

Bacteriophage P22 linear DNA molecules are a set of circularly permuted sequences with ends located in a limited region of the physical map. This mature form of the viral chromosome is cut in headful lengths from a concatemeric precursor during DNA encapsulation. Packaging of P22 DNA begins at a specific site, which we have termed pat, and then proceeds sequentially to cut lengths of DNA slightly longer than one complete set of P22 genes (Tye et al., 1974b). The sites of DNA maturation events have been located on the physical map of EcoRI cleavage sites in P22 DNA. EcoRI digestion products of mature P22 wild-type DNA were compared with EcoRI fragments of two deletion and two insertion mutant DNAs. These mutations decrease or increase the length of the genome, but do not alter the DNA encapsulation mechanism. Thus the position of mature molecular ends relative to EcoRI restriction sites is different in each mutant, and comparison of the digests shows which fragments come from the ends of linear molecules. From the positions of the ends of molecules processed in sequential headfuls, the location of pat and the direction of encapsulation relative to the I’22 map were deduced. The pat site lies in EcoRI fragment A, 4.1 x lo3 basepairs from EcoRI cleavage site 1. Sequential packaging of the concatemer is initiated at pat and proceeds in the counterclockwise direction relative to the circular map of P22. One-third of the linears in a population are cut from the concatemer at poac, and most packaging sequences do not extend beyond four headfuls. Fragment D is produced by &oRI cleavage at a site near the end of a linear chromosome which has been encapsulated starting at pat. The position of the pat site is therefore defined by one end of fragment D. The pat site is not located near genes 12 and 18, the only known site for initiation of P22 DNA replication, but lies among late genes at a position on the physical gene map approximately analogous to the cohesive end site (~08) of bacteriophage h at which X DNA is cleaved during encapsulation. Our results suggest that P22 and X DNA maturation mechanisms have many common properties.