Literature DB >> 25256747

Controlling DNA degradation from a distance: a new role for the Mu transposition enhancer.

Wonyoung Choi1, Rudra P Saha, Sooin Jang, Rasika M Harshey.   

Abstract

Phage Mu is unique among transposable elements in employing a transposition enhancer. The enhancer DNA segment is the site where the transposase MuA binds and makes bridging interactions with the two Mu ends, interwrapping the ends with the enhancer in a complex topology essential for assembling a catalytically active transpososome. The enhancer is also the site at which regulatory proteins control divergent transcription of genes that determine the phage lysis-lysogeny decision. Here we report a third function for the enhancer - that of regulating degradation of extraneous DNA attached to both ends of infecting Mu. This DNA is protected from nucleases by a phage protein until Mu integrates into the host chromosome, after which it is rapidly degraded. We find that leftward transcription at the enhancer, expected to disrupt its topology within the transpososome, blocks degradation of this DNA. Disruption of the enhancer would lead to the loss or dislocation of two non-catalytic MuA subunits positioned in the transpososome by the enhancer. We provide several lines of support for this inference, and conclude that these subunits are important for activating degradation of the flanking DNA. This work also reveals a role for enhancer topology in phage development.
© 2014 John Wiley & Sons Ltd.

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Year:  2014        PMID: 25256747      PMCID: PMC4213243          DOI: 10.1111/mmi.12781

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  70 in total

1.  Efficient Mu transposition requires interaction of transposase with a DNA sequence at the Mu operator: implications for regulation.

Authors:  M Mizuuchi; K Mizuuchi
Journal:  Cell       Date:  1989-07-28       Impact factor: 41.582

2.  Interaction of distinct domains in Mu transposase with Mu DNA ends and an internal transpositional enhancer.

Authors:  P C Leung; D B Teplow; R M Harshey
Journal:  Nature       Date:  1989-04-20       Impact factor: 49.962

Review 3.  Site-specific inversion: enhancers, recombination proteins, and mechanism.

Authors:  N L Craig
Journal:  Cell       Date:  1985-07       Impact factor: 41.582

4.  The overproduction and characterization of the bacteriophage Mu regulatory DNA-binding protein ner.

Authors:  P P Tolias; M S Dubow
Journal:  Virology       Date:  1986-01-30       Impact factor: 3.616

5.  Transposition of bacteriophage mu DNA: expression of the A and B proteins from lambda pL and analysis of infecting mu DNA.

Authors:  G Chaconas; G Gloor; J L Miller; D L Kennedy; E B Giddens; C R Nagainis
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1984

6.  Predominant integration end products of infecting bacteriophage Mu DNA are simple insertions with no preference for integration of either Mu DNA strand.

Authors:  G Chaconas; D L Kennedy; D Evans
Journal:  Virology       Date:  1983-07-15       Impact factor: 3.616

7.  Regulation of Mu transposition. II. The escherichia coli HimD protein positively controls two repressor promoters and the early promoter of bacteriophage Mu.

Authors:  N Goosen; M van Heuvel; G F Moolenaar; P van de Putte
Journal:  Gene       Date:  1984-12       Impact factor: 3.688

8.  Infecting bacteriophage mu DNA forms a circular DNA-protein complex.

Authors:  R M Harshey; A I Bukhari
Journal:  J Mol Biol       Date:  1983-06-25       Impact factor: 5.469

9.  DNA-protein complexes during attachment-site synapsis in Mu DNA transposition.

Authors:  C F Kuo; A H Zou; M Jayaram; E Getzoff; R Harshey
Journal:  EMBO J       Date:  1991-06       Impact factor: 11.598

10.  Structural aspects of a higher order nucleoprotein complex: induction of an altered DNA structure at the Mu-host junction of the Mu type 1 transpososome.

Authors:  B D Lavoie; B S Chan; R G Allison; G Chaconas
Journal:  EMBO J       Date:  1991-10       Impact factor: 11.598

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  3 in total

1.  Fluorescent fusions of the N protein of phage Mu label DNA damage in living cells.

Authors:  Matthew V Kotlajich; Jun Xia; Yin Zhai; Hsin-Yu Lin; Catherine C Bradley; Xi Shen; Qian Mei; Anthony Z Wang; Erica J Lynn; Chandan Shee; Li-Tzu Chen; Lei Li; Kyle M Miller; Christophe Herman; P J Hastings; Susan M Rosenberg
Journal:  DNA Repair (Amst)       Date:  2018-09-14

2.  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

3.  Transposition Behavior Revealed by High-Resolution Description of Pseudomonas Aeruginosa Saltovirus Integration Sites.

Authors:  Gilles Vergnaud; Cédric Midoux; Yann Blouin; Maria Bourkaltseva; Victor Krylov; Christine Pourcel
Journal:  Viruses       Date:  2018-05-07       Impact factor: 5.048

  3 in total

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