Evidence for a conservative pathway of transposition of bacteriophage Mu
- 1 May 1983
- journal article
- letter
- Published by Springer Nature in Nature
- Vol. 303 (5912) , 84-86
- https://doi.org/10.1038/303084a0
Abstract
During its lytic cycle bacteriophage Mu uses repeated transposition as a mode of DNA synthesis. These transpositional events are undoubtedly replicative, and presumably semi-conservative. In a Mu lysogen this type of transposition can start immediately after prophage induction. However, in an infective cycle the Mu genome (which is injected into the host cell as a linear molecule flanked by short random sequences of bacterial DNA) must first become integrated into the host chromosome. Little is known about how this occurs apart from the fact that the bacterial sequences at either end of the Mu genome are lost in the process1. The integration is thus similar to a transposition event. In an attempt to determine whether this type of Mu transposition (between a linear donor molecule and a circular recipient) is also semi-conservative we have analysed the progeny phage arising from an infective cycle in which the parental DNA was heterozygous for a known genetic marker. The expectation is that if integration of the infecting Mu genome occurs by a single semi-conservative transpositional event then pure phage bursts should be produced as the genetic information on only one strand would be preserved throughout the lytic cycle. The experiments reported here do not support this expectation in that the infected cells yield mixed bursts, suggesting that Mu integration is a conservative, rather than a semi-conservative event.Keywords
This publication has 8 references indexed in Scilit:
- Conservative integration of bacteriophage Mu DNA into pBR322 plasmid.Proceedings of the National Academy of Sciences, 1982
- Transposition Studies Using a Co1E1 Derivative Carrying Bacteriophage MuCold Spring Harbor Symposia on Quantitative Biology, 1981
- The isolation and characteristics of plasmids derived from the insertion of MupAp1 into pML2: Their behavior during transpositionPlasmid, 1980
- Transfection with Mu-DNAVirology, 1977
- Transfection of Escherichia coli by Mu DNAMolecular Genetics and Genomics, 1976
- Mismatch repair in heteroduplex DNA.Proceedings of the National Academy of Sciences, 1975
- Electron microscope heteroduplex study of the heterogeneity of Mu phage and prophage DNAVirology, 1974
- One way to do experiments on gene conversion?Molecular Genetics and Genomics, 1970