Dynamics of Genome Architecture in Rhizobium sp. Strain NGR234
DNA, Bacterial
Recombination, Genetic
0301 basic medicine
[SDV]Life Sciences [q-bio]
info:eu-repo/classification/ddc/580
612
Polymerase Chain Reaction
Electrophoresis, Gel, Pulsed-Field
[SDV] Life Sciences [q-bio]
Evolution, Molecular
03 medical and health sciences
Phenotype
DNA Transposable Elements
Replicon
Symbiosis
Genome, Bacterial
Rhizobium
DOI:
10.1128/jb.184.1.171-176.2002
Publication Date:
2002-07-27T10:01:09Z
AUTHORS (7)
ABSTRACT
ABSTRACT
Bacterial genomes are usually partitioned in several replicons, which are dynamic structures prone to mutation and genomic rearrangements, thus contributing to genome evolution. Nevertheless, much remains to be learned about the origins and dynamics of the formation of bacterial alternative genomic states and their possible biological consequences. To address these issues, we have studied the dynamics of the genome architecture in
Rhizobium
sp. strain NGR234 and analyzed its biological significance. NGR234 genome consists of three replicons: the symbiotic plasmid pNGR234
a
(536,165 bp), the megaplasmid pNGR234
b
(>2,000 kb), and the chromosome (>3,700 kb). Here we report that genome analyses of cell siblings showed the occurrence of large-scale DNA rearrangements consisting of cointegrations and excisions between the three replicons. As a result, four new genomic architectures have emerged. Three consisted of the cointegrates between two replicons: chromosome-pNGR234
a
, chromosome-pNGR234
b
, and pNGR234
a
-pNGR234
b
. The other consisted of a cointegrate of the three replicons (chromosome-pNGR234
a
-pNGR234
b
). Cointegration and excision of pNGR234
a
with either the chromosome or pNGR234
b
were studied and found to proceed via a Campbell-type mechanism, mediated by insertion sequence elements. We provide evidence showing that changes in the genome architecture did not alter the growth and symbiotic proficiency of
Rhizobium
derivatives.
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