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SRX7916263: GSM4413105: 20180327.A-Olga_NullN1_R1; Burkholderia cenocepacia H111; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 30.1M spots, 2.1G bases, 1.1Gb downloads

Submitted by: NCBI (GEO)
Study: An investigation of Burkholderia cepacia complex methylomes via SMRT sequencing and mutant analysis
show Abstracthide Abstract
While nucleotide sequences determine an organism's proteins, methylation of the nucleotides themselves can confer additional properties. In bacteria, differences in methylation can be used to identify incoming DNA, for example from bacteriophages. Restriction enzymes detect the methylation status at specific sequence motifs, and cleave improperly methylated, foreign DNA. Furthermore, methylation of key genetic regions can influence gene expression and hence phenotype. In this study, we determined the methylated motifs of three strains from the closely-related Burkholderia cepacia complex of opportunistic pathogens. Three of these motifs were novel, while two are methylated throughout this group of bacteria and beyond and had already been assigned putative causative genes. To investigate the contribution of the enzymes that methylate and cut DNA, we deleted the genes encoding them from a representative strain. We found that these genes are important for traits including motility, biofilm formation, cell shape and production of iron acquisition elements. The mutant strain showed marked defects in replicon partitioning and was more efficient at acquiring foreign DNA, illustrating the importance of methylation in maintaining genome integrity. Interestingly, we found that one methylase, part of an integrated bacteriophage genome, was essential for maintaining the phage in a dormant state. Overall design: Burkholderia cepacia complex epigenetics
Sample: 20180327.A-Olga_NullN1_R1
SAMN14382706 • SRS6322650 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Cells were flash frozen on dry ice. The RNA was obtained using a hot phenol protocol (Pessi et al 2007). The cDNA was prepared and NuGen libraries obtained. RNA libraries were prepared using Ovation Complete Prokaryotic RNA-Seq DR Muliplex System NuGen
Experiment attributes:
GEO Accession: GSM4413105
Links:
Runs: 1 run, 30.1M spots, 2.1G bases, 1.1Gb
Run# of Spots# of BasesSizePublished
SRR1131177630,113,1592.1G1.1Gb2021-06-01

ID:
10351198

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