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SRX15590246: GSM6212705: Experiment #2 Time 0 #6; Synechococcus elongatus PCC 7942 = FACHB-805; OTHER
1 ILLUMINA (Illumina HiSeq 2000) run: 4.2M spots, 210.4M bases, 77.8Mb downloads

External Id: GSM6212705_r1
Submitted by: University of California San Diego
Study: Transcriptomic and phenomic investigations reveal elements in biofilm repression and formation in the cyanobacterium Synechococcus elongatus PCC 7942 [RB-TnSeq]
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Biofilm formation by photosynthetic organisms is a complex behavior that serves multiple functions in the environment. Biofilm formation in the unicellular cyanobacterium Synechococcus elongatus PCC 7942 is regulated in part by a set of small secreted proteins that promotes biofilm formation and a self-suppression mechanism that prevents their expression. Little is known about the regulatory and structural components of the biofilms in PCC 7942, or response to the suppressor signal(s). We performed transcriptomics (RNA-Seq) and phenomics (RB-TnSeq) screens that identified four genes involved in biofilm formation and regulation, more than 25 additional candidates that may impact biofilm formation, and revealed the transcriptomic adaptation to the biofilm state. In so doing, we compared the effectiveness of these two approaches for gene discovery. Overall design: Expression profiling by high throughput sequencing (RNA-seq) comparing WT and the pilB::Tn5 biofilm forming mutant strain over time
Sample: Experiment #2 Time 0 #6
SAMN28860411 • SRS13292268 • All experiments • All runs
Library:
Name: GSM6212705
Instrument: Illumina HiSeq 2000
Strategy: OTHER
Source: GENOMIC
Selection: other
Layout: SINGLE
Construction protocol: Frozen cell pellets were thawed and genomic DNA was extracted using a phenol-chloroform and ethanol precipitation protocol, as previously described by Clerico, et al 2007. Barcodes of transposon insertions in the pooled library were PCR amplified. Primers for this amplification contained adapters for Illumina sequencing, experiment-specific barcodes, and heterogenous spacers for enhanced length diversity, as described by Wetmore, et al. (2015). Amplicons were assessed by gel electrophoresis and purified using a PCR-purification kit (Zymo).
Runs: 1 run, 4.2M spots, 210.4M bases, 77.8Mb
Run# of Spots# of BasesSizePublished
SRR195381994,207,915210.4M77.8Mb2022-06-06

ID:
22195635

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