Document Detail


Genome sequences of three agrobacterium biovars help elucidate the evolution of multichromosome genomes in bacteria.
MedLine Citation:
PMID:  19251847     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The family Rhizobiaceae contains plant-associated bacteria with critical roles in ecology and agriculture. Within this family, many Rhizobium and Sinorhizobium strains are nitrogen-fixing plant mutualists, while many strains designated as Agrobacterium are plant pathogens. These contrasting lifestyles are primarily dependent on the transmissible plasmids each strain harbors. Members of the Rhizobiaceae also have diverse genome architectures that include single chromosomes, multiple chromosomes, and plasmids of various sizes. Agrobacterium strains have been divided into three biovars, based on physiological and biochemical properties. The genome of a biovar I strain, A. tumefaciens C58, has been previously sequenced. In this study, the genomes of the biovar II strain A. radiobacter K84, a commercially available biological control strain that inhibits certain pathogenic agrobacteria, and the biovar III strain A. vitis S4, a narrow-host-range strain that infects grapes and invokes a hypersensitive response on nonhost plants, were fully sequenced and annotated. Comparison with other sequenced members of the Alphaproteobacteria provides new data on the evolution of multipartite bacterial genomes. Primary chromosomes show extensive conservation of both gene content and order. In contrast, secondary chromosomes share smaller percentages of genes, and conserved gene order is restricted to short blocks. We propose that secondary chromosomes originated from an ancestral plasmid to which genes have been transferred from a progenitor primary chromosome. Similar patterns are observed in select Beta- and Gammaproteobacteria species. Together, these results define the evolution of chromosome architecture and gene content among the Rhizobiaceae and support a generalized mechanism for second-chromosome formation among bacteria.
Authors:
Steven C Slater; Barry S Goldman; Brad Goodner; João C Setubal; Stephen K Farrand; Eugene W Nester; Thomas J Burr; Lois Banta; Allan W Dickerman; Ian Paulsen; Leon Otten; Garret Suen; Roy Welch; Nalvo F Almeida; Frank Arnold; Oliver T Burton; Zijin Du; Adam Ewing; Eric Godsy; Sara Heisel; Kathryn L Houmiel; Jinal Jhaveri; Jing Lu; Nancy M Miller; Stacie Norton; Qiang Chen; Waranyoo Phoolcharoen; Victoria Ohlin; Dan Ondrusek; Nicole Pride; Shawn L Stricklin; Jian Sun; Cathy Wheeler; Lindsey Wilson; Huijun Zhu; Derek W Wood
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.     Date:  2009-02-27
Journal Detail:
Title:  Journal of bacteriology     Volume:  191     ISSN:  1098-5530     ISO Abbreviation:  J. Bacteriol.     Publication Date:  2009 Apr 
Date Detail:
Created Date:  2009-04-01     Completed Date:  2009-04-23     Revised Date:  2013-06-02    
Medline Journal Info:
Nlm Unique ID:  2985120R     Medline TA:  J Bacteriol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  2501-11     Citation Subset:  IM    
Affiliation:
Virginia Bioinformatics Institute, Washington St., MC 0477, Blacksburg, VA 24060, USA.
Data Bank Information
Bank Name/Acc. No.:
GENBANK/CP000628;  CP000629;  CP000630;  CP000631;  CP000632;  CP000633;  CP000634;  CP000635;  CP000636;  CP000637;  CP000638;  CP000639
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MeSH Terms
Descriptor/Qualifier:
Computational Biology / methods
Conserved Sequence
DNA, Bacterial / chemistry,  genetics*
Evolution, Molecular*
Gene Order
Genome, Bacterial*
Molecular Sequence Data
Phylogeny
Rhizobium / genetics*
Sequence Analysis, DNA
Synteny
Grant Support
ID/Acronym/Agency:
52005125//Howard Hughes Medical Institute
Chemical
Reg. No./Substance:
0/DNA, Bacterial
Comments/Corrections

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