Affiliation:
1. Gene Regulation and Chromosome Biology Laboratory, National Cancer Institute, CCR, NCI-Frederick, Frederick, Maryland 21702-1201
Abstract
ABSTRACT
The P1
par
family of active plasmid partition systems consists of at least six members, broadly distributed in a variety of plasmid types and bacterial genera. Each encodes two Par proteins and contains a
cis
-acting
parS
site. Individual
par
systems can show distinct species specificities; the proteins from one type cannot function with the
parS
site of another. P1
par
-versus-P7
par
specificity resides within two hexamer BoxB repeats encoded by
parS
that contact the ParB protein near the carboxy terminus. Here, we examine the species specificity differences between
Yersinia pestis
pMT1
parS
and
Escherichia coli
P1 and P7
parS
. pMT1
parS
site specificity could be altered to that of either P1 or P7 by point mutation changes in the BoxB repeats. Just one base change in a single BoxB repeat sometimes sufficed. The BoxB sequence appears to be able to adopt a number of forms that define exclusive interactions with different ParB species. The looped
parS
structure may facilitate this repertoire of interaction specificities. Different P1
par
family members have different partition-mediated incompatibility specificities. This property defines whether two related plasmids can coexist in the same cell and is important in promoting the evolution of new plasmid species. BoxB sequence changes that switch species specificity between P1, P7, and pMT1 species switched partition-mediated plasmid incompatibility in concert. Thus, there is a direct mechanistic link between species specificity and partition-mediated incompatibility, and the BoxB-ParB interaction can be regarded as a special mechanism for facilitating plasmid evolution.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
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