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Series GSE15889 Query DataSets for GSE15889
Status Public on May 01, 2009
Title Genome Variation in the Symbiotic Nitrogen-Fixing Bacterium Sinorhizobium meliloti
Platform organism Sinorhizobium meliloti 1021
Sample organism Sinorhizobium meliloti
Experiment type Genome variation profiling by array
Summary Differences in genome size and gene content are among the most important signatures of microbial adaptation and genome evolution. Here, we investigated the patterns of genome variation among strains of the symbiotic nitrogen-fixing bacterium Sinorhizobium meliloti. Using the sequenced strain Rm1021 as a reference, the genome size and gene content variations were analyzed among ten diverse natural strains, through pulse field gel electrophoresis (PFGE) and whole-genome microarray hybridizations. Our PFGE analysis showed a genome size range of 6.45-7.01Mbp, with the greatest variation arising from the pSymA replicon, followed by that of pSymB. No observable size difference was evident among the chromosomes. Consistent with this pattern of size differences, 41.2% of ORFs on pSymA were variably absent/present, followed by 12.7% on pSymB, and 3.7% on the chromosome. However, the percentages of ORFs that were variably duplicated were more evenly distributed among the three replicons, 11.0%, 16.5% and 15.3% respectively for ORFs on pSymA, pSymB and the chromosome. Among the 10 strains, the percentages of absent ORFs ranged from 1.51% to 6.35% and those of duplicated ORFs ranged from 0.27% to 8.56%. Our analyses showed that host plants, geographic origins, multilocus enzyme electrophoretic types, and replicon sizes had little influence on the distribution patterns of absent or duplicated ORFs. The proportions of ORFs that were either variably absent/present or variably duplicated differed greatly among the functional categories, for each of the three replicons as well as for the whole genome. Interestingly, we observed positive correlations among the three replicons in their numbers of absent ORFs as well as the numbers of duplicated ORFs, consistent with coordinated gene gains/losses in this important bacterium in nature.
microarray:Sm6kOligo
 
Overall design A total of 12 strains were included for the microarray analyses in this study. The 12 strains included two reference strains and ten other natural strains. Reference strain Rm1021 was the strain with a completely sequenced genome, from which the whole genome microarray was based on (Krol et al. 2004). The second reference strain RmF909 was derived from strain Rm1021 but with a deletion of 575 ORFs located on the megaplasmid pSymB (genomic location 106724-735431, Charles et al. 1991). The two reference strains were used for positive and negative controls in our microarray hybridization experiments and for establishing threshold values for determining whether an ORF is present or absent among natural strains.
 
Contributor(s) Guo H, Sun S, Eardly B, Finan T, Xu J
Citation(s) 19935910
Submission date Apr 29, 2009
Last update date Mar 21, 2012
Contact name HONG GUO
Organization name MCMASTER UNIVERSITY
Department BIOLOGY
Lab DR.XU,JP
Street address 1280Main St. West
City Hamilton
State/province Ontario
ZIP/Postal code L8S 4K1
Country Canada
 
Platforms (1)
GPL8499 sm6koligo
Samples (14)
GSM399002 Control Sm 1021 replicate1
GSM399003 Control Sm 1021 replicate2
GSM399004 Control1021/F909
Relations
BioProject PRJNA117055

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE15889_RAW.tar 23.4 Mb (http)(custom) TAR (of GPR)
Processed data included within Sample table

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