Partial replicas of UV-irradiated bacteriophage T4 genomes and their role in multiplicity reactivation

A physicochemical study was made of the replication and transmission of UV-irradiated T4 genomes. The data presented in this paper justify the following conclusions. (i) For both low and high multiplicity of infection there was abundant replication from UV-irradiated parental templates. It exceeded by far the efficiency predicted by the hypothesis that a single lethal hit completely prevents replication of the killed phage DNA: i.e., some dead phage particles must replicate parts of thier DNA. (ii) Replication of the UV-irradiated DNA was repetitive as shown by density reversal experiments. (iii) Newly synthesized progeny DNA originating from UV-irradiated templates appeared as significantly shorter segments of the genomes than progeny DNA produced from non-UV-irradiated templates. A good correlation existed between the number of UV hits and the number of random cuts that would be needed to reduce replication fragments to the length observed. (iv) The contribution of UV-irradiated parental DNA among progeny phage in multiplicity reactivation was disposed in shorter subunits than was the DNA from unirradiated parental phage. It is important to emphasize that it was mainly in the form of replicative hybrid. These conclusions appear to justify excluding interparental recombination as a prerequisite for multiplicity reactivation. They lead directly to some form of partial replica hypothesis for multiplicity reactivation.

[1]  R. Miller,et al.  Marker rescue and partial replication of bacteriophage T7 DNA. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[2]  A. Doermann,et al.  Absence of interparental recombination in multiplicity reconstitution from incomplete bacteriophage T4 genomes , 1976, Journal of virology.

[3]  A. Doermann,et al.  Repetitive DNA replication of the incomplete genomes of phage T4 petite particles. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[4]  T. R. Broker,et al.  Molecular and genetic recombination of bacteriophage T4. , 1975, Annual review of genetics.

[5]  K. Carlson,et al.  Host-Mediated Repair of Discontinuities in DNA From T4 Bacteriophage , 1973, Journal of virology.

[6]  K. Carlson,et al.  Multiple and Specific Initiation of T4 DNA Replication , 1973, Journal of virology.

[7]  H. Delius,et al.  Structure of the replicating DNA from bacteriophage T4. , 1971, Proceedings of the National Academy of Sciences of the United States of America.

[8]  S. Litwin,et al.  Molecular Recombination in T4 Bacteriophage Deoxyribonucleic Acid , 1970, Journal of virology.

[9]  M. Mitchell,et al.  Restoration by Chloramphenicol of Bacteriophage Production in Escherichia coli B Infected with a Ligase-Deficient Amber Mutant , 1969, Journal of virology.

[10]  S. Litwin,et al.  Interpretation of Sucrose Gradient Sedimentation Pattern of Deoxyribonucleic Acid Fragments Resulting from Random Breaks , 1969, Journal of virology.

[11]  A. Kozinski Molecular recombination in the ligase negative T4 amber mutant. , 1968, Cold Spring Harbor Symposia on Quantitative Biology.

[12]  R. James,et al.  Molecular Recombination in T4 Bacteriophage Deoxyribonucleic Acid I. Tertiary Structure of Early Replicative and Recombining Deoxyribonucleic Acid , 1967, Journal of virology.

[13]  A. Kozinski,et al.  Fragmentary transfer of P32 labeled parental DNA to progeny phage. 3. Incorporation of a single parental fragment to the progeny molecule. , 1966, Virology.

[14]  N. A. Barricelli,et al.  Radiation-genetic evidence that only one of the two DNAstrands injected by phage T4 transmits the genetic information to the progeny. , 1965, Virology.

[15]  A. Kozinski,et al.  Early intracellular events in the replication of T4 phage DNA. I. Complex formation of replicative DNA. , 1965, Proceedings of the National Academy of Sciences of the United States of America.

[16]  P. Shannon,et al.  REPLICATIVE FRAGMENTATION IN T4 PHAGE: INHIBITION BY CHLORAMPHENICOL. , 1963, Proceedings of the National Academy of Sciences of the United States of America.

[17]  A. Kozinski,et al.  Fragmentary transfer of P32-labeled parental DNA to progeny phage. II. The average size of the transferred parental fragment. Two-cycletransfer. Repair of the polynucleotide chain after fragmentation. , 1963, Virology.

[18]  N. A. Barricelli,et al.  An analytical approach to the problems of phage recombination and reproduction. III. Cross reactivation. , 1961, Virology.

[19]  A. Kozinski Fragmentary transfer of P32-labeled parental DNA to progeny phage. , 1961, Virology.

[20]  Nils Aall Barricelli,et al.  An analytical approach to the problems of phage recombination and reproduction: I. Multiplicity reactivation and the nature of radiation damages , 1960 .

[21]  D. R. Krieg A study of gene action in ultraviolet-irradiated bacteriophage T4. , 1959, Virology.

[22]  R. Dulbecco,et al.  Genetic Recombinations Leading to Production of Active Bacteriophage from Ultraviolet Inactivated Bacteriophage Particles. , 1949, Genetics.

[23]  S. Luria Reactivation of Irradiated Bacteriophage by Transfer of Self-Reproducing Units. , 1947, Proceedings of the National Academy of Sciences of the United States of America.