Literature DB >> 6302516

Evidence for a conservative pathway of transposition of bacteriophage Mu.

J E Akroyd, N Symonds.   

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 process. 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.

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Year:  1983        PMID: 6302516     DOI: 10.1038/303084a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  12 in total

1.  DNA repair by the cryptic endonuclease activity of Mu transposase.

Authors:  Wonyoung Choi; Rasika M Harshey
Journal:  Proc Natl Acad Sci U S A       Date:  2010-02-18       Impact factor: 11.205

2.  Phage Mu transposase: deletion of the carboxy-terminal end does not abolish DNA-binding activity.

Authors:  M Betermier; R Alazard; F Ragueh; E Roulet; A Toussaint; M Chandler
Journal:  Mol Gen Genet       Date:  1987-11

3.  Chromosomal integration mechanism of infecting mu virion DNA.

Authors:  T K Au; Pushpa Agrawal; Rasika M Harshey
Journal:  J Bacteriol       Date:  2006-03       Impact factor: 3.490

4.  In vivo mutagenesis of bacteriophage Mu transposase.

Authors:  A Toussaint; L Desmet; M Faelen; R Alazard; M Chandler; M Pato
Journal:  J Bacteriol       Date:  1987-12       Impact factor: 3.490

Review 5.  The Mu gem operon: its role in gene expression, recombination and cell cycle.

Authors:  P Ghelardini; R La Valle; L Paolozzi
Journal:  Genetica       Date:  1994       Impact factor: 1.082

6.  Extrachromosomal copies of transposon Tc1 in the nematode Caenorhabditis elegans.

Authors:  K Ruan; S W Emmons
Journal:  Proc Natl Acad Sci U S A       Date:  1984-07       Impact factor: 11.205

Review 7.  Application of the bacteriophage Mu-driven system for the integration/amplification of target genes in the chromosomes of engineered Gram-negative bacteria--mini review.

Authors:  Valerii Z Akhverdyan; Evgueni R Gak; Irina L Tokmakova; Nataliya V Stoynova; Yurgis A V Yomantas; Sergey V Mashko
Journal:  Appl Microbiol Biotechnol       Date:  2011-06-23       Impact factor: 4.813

8.  Repair of transposable phage Mu DNA insertions begins only when the E. coli replisome collides with the transpososome.

Authors:  Sooin Jang; Rasika M Harshey
Journal:  Mol Microbiol       Date:  2015-06-06       Impact factor: 3.501

Review 9.  Regulation of bacteriophage Mu transposition.

Authors:  A Toussaint; M J Gama; J Laachouch; G Maenhaut-Michel; A Mhammedi-Alaoui
Journal:  Genetica       Date:  1994       Impact factor: 1.082

10.  Synchronization of bacteriophage Mu DNA replicative transposition: analysis of the first round after induction.

Authors:  C Reich; B T Waggoner; M L Pato
Journal:  EMBO J       Date:  1984-07       Impact factor: 11.598

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