The phi X174-type primosome promotes replisome assembly at the site of recombination in bacteriophage Mu transposition
Open Access
- 15 November 1997
- journal article
- research article
- Published by Springer Nature in The EMBO Journal
- Vol. 16 (22) , 6886-6895
- https://doi.org/10.1093/emboj/16.22.6886
Abstract
Initiation of Escherichia coli DNA synthesis primed by homologous recombination is believed to require the φX174‐type primosome, a mobile priming apparatus assembled without the initiator protein DnaA. We show that this primosome plays an essential role in bacteriophage Mu DNA replication by transposition. Upon promoting transfer of Mu ends to target DNA, the Mu transpososome undergoes transition to a pre‐replisome that permits initiation of DNA synthesis only in the presence of primosome assembly proteins PriA, DnaT, DnaB and DnaC. These assembly proteins promote the engagement of primase and DNA polymerase III holoenzyme, initiating semi‐discontinuous replication preferentially at the Mu left end. The results indicate that these proteins play a crucial role in promoting replisome assembly on a recombination intermediate.Keywords
This publication has 42 references indexed in Scilit:
- The DNA replication protein PriA and the recombination protein RecG bind D-loopsJournal of Molecular Biology, 1997
- DNA transposition: Assembly of a jumping gene machineCurrent Biology, 1996
- The Ordered Assembly of the φX174-type PrimosomeJournal of Biological Chemistry, 1996
- The Ordered Assembly of the φX174-type PrimosomeJournal of Biological Chemistry, 1996
- Exchanging partners: recombination in E. coliTrends in Genetics, 1996
- Disassembly of the Mu transposase tetramer by the ClpX chaperone.Genes & Development, 1995
- Transcriptional activation of ColE1 DNA synthesis by displacement of the nontranscribed strandCell, 1987
- Transposition of Mu DNA: Joining of Mu to target DNA can be uncoupled from cleavage at the ends of MuCell, 1987
- Transpososomes: Stable protein-DNA complexes involved in the in vitro transposition of bacteriophage Mu DNACell, 1987
- Replication initiated at the origin (oriC) of the E. coli chromosome reconstituted with purified enzymesCell, 1984