RecA Regulation by RecU and DprA During Bacillus subtilis Natural Plasmid Transformation

Natural plasmid transformation plays an important role in the dissemination of antibiotic resistance genes in bacteria. During this process, RecA physically interacts with RecU, RecX, and DprA. These three proteins are required for plasmid transformation, but RecA is not. , DprA recruits RecA onto S...

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Published in:Frontiers in microbiology Vol. 9; p. 1514
Main Authors: Serrano, Ester, Carrasco, Begoña, Gilmore, Jamie L, Takeyasu, Kunio, Alonso, Juan C
Format: Journal Article
Language:English
Published: Switzerland Frontiers Media S.A 11-07-2018
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Summary:Natural plasmid transformation plays an important role in the dissemination of antibiotic resistance genes in bacteria. During this process, RecA physically interacts with RecU, RecX, and DprA. These three proteins are required for plasmid transformation, but RecA is not. , DprA recruits RecA onto SsbA-coated single-stranded (ss) DNA, whereas RecX inhibits RecA filament formation, leading to net filament disassembly. We show that a null (Δ ) mutation suppresses the plasmid transformation defect of competent Δ cells, and that RecU is essential for both chromosomal and plasmid transformation in the Δ context. RecU inhibits RecA filament growth and facilitates RecA disassembly from preformed filaments. Increasing SsbA concentrations additively contributes to RecU-mediated inhibition of RecA filament extension. DprA is necessary and sufficient to counteract the negative effect of both RecU and SsbA on RecA filament growth onto ssDNA. DprA-SsbA activates RecA to catalyze DNA strand exchange in the presence of RecU, but this effect was not observed if RecU was added prior to RecA. We propose that DprA contributes to RecA filament growth onto any internalized SsbA-coated ssDNA. When the ssDNA is homologous to the recipient, DprA antagonizes the inhibitory effect of RecU on RecA filament growth and helps RecA to catalyze chromosomal transformation. On the contrary, RecU promotes RecA filament disassembly from a heterologous (plasmid) ssDNA, overcoming an unsuccessful homology search and favoring plasmid transformation. The DprA-DprA interaction may promote strand annealing upon binding to the complementary plasmid strands and facilitating thereby plasmid transformation rather than through a mediation of RecA filament growth.
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Reviewed by: Vladimir Bidnenko, INRA Centre Jouy-en-Josas, France; Aida Kalantari, Duke University, United States
This article was submitted to Microbial Physiology and Metabolism, a section of the journal Frontiers in Microbiology
Edited by: Ivan Mijakovic, Chalmers University of Technology, Sweden
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2018.01514