Q 38 Reprinted—from Abstramm, 7th iIntexnaetene! Congress of Microbiolegy, Stockholm, 1958, pp. 58-60. Extranuclear transmission of the 7 compatibility fac- to in E. coli. Joshua Lederberg,”Departments of Genetics and Medical Genetics, University of Wiscon- sin, Madison 6, Wisconsin, U.S.A. The mating types of E. coli include F females and F males, the latter being determined by the presence of a readily contagious factor "F". A number of lines of evidence converge to suggest that this is inherited outside the chromosomal system of linked markers which encompasses most of the known heredity of E. coli: 1) in crosses of FY x F’, virtue ally all of the progeny arc F° while other markers segregate in characteristic ratios. 2) When an F culture is seeded with a few F’ cells, the F° charac- ter spreads through the entire population, indicating that it multiplies more rapidly than the other genes. 3) After pairing with an F' cell, an F cell gives rise to a pura F clone; in comparable matings of F x Hfr (high frequency of recombination with respect to other markers) the exconjugant F clone invariably segregates a mixture of unaltered parental and recombinant types. k) FY is transferred more rapidly and efficiently than any other known markers, and in F’ x F crosses, shows no linkage to any other marker. 5) As described by Y. Hirota, the F" factor can be efficiently removed from a population of F° cells by treating them with. acridine dyes, especially acridine orange. These findings suagest that the Ft cell carries an oxtra- nuclear factor, i.e., a plasmid, which is rapidly and efficiently transferred to F cells during bricf con- tact. Ia Tany respects, the inheritance of F is analogous to that of the factor which governs the trait colicinogeny as analysed by Fredericq. The mating behavior of Hfr mutants, the instability of some of these to give infective Ft reversions auld the segregation of the_Hfr in various linkage re lationships in Hfr x F crosses suggest that the. Hfr mating types represent the fixation of the F factor at specific chromosomal loci. The deerth of recombinants given by FY com- pared to Hfr has provoked the hypothesis that F is instrinsically sterile, and that its recombin- ational fertility depends on spontaneous mutation to Hfr. Such mutants undoubtedly occur, but it is difficult to assess their role in F fertility without an accurate measure of the mutation rate. The regularity with which F x F crosses give F' progeny argues against the necessary role of stable, non-infective Hfr mutants similar to the type. Hfro, Control] experiments have shown that the Cavallarity of F’ progeny is not duc to secondary reinfection. It is still possible that in addition to occasional Hfr mutations, the more fertile cells in an F° culture have experienced more transient changes in the quality or position of the F agent they carry.