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Series GSE106171 Query DataSets for GSE106171
Status Public on Oct 26, 2017
Title Identification of RNAs that co-purify with the Caulobacter sRNA, GsrN
Organism Caulobacter vibrioides
Experiment type Expression profiling by high throughput sequencing
Summary Purpose: To identify RNAs that interact with GsrN, a small regulatory RNA from Caulobacter crescentus.
Methods: Pseudomonas phage 7 (PP7) viral coat protein fused to maltose binding protein (MBP) was immobilized on amylose resin. PP7 coat protein binds to PP7 RNA hairpins (PP7hp). A strain expressing GsrN tagged with a genetically encoded PP7hp at base 37 (GsrN(37)-PP7hp) was captured on this column, washed, and eluted in biological triplicate (pos_rep). As a negative control, we incubated the PP7 coat protein column with independent duplicate lysates from a Caulobacter strain expressing PP7hp fused to a non-functional 3' isoform of GsrN (mock). We generated RNA-seq libraries for each of three independent GsrN(37)-PP7hp fractions, and the duplicate mock fractions.
Results: We quantified levels of RNAs in the GsrN(37)-PP7hp (pos) fractions with fractions from parallel PP7hp-3'GsrN(mock) pull-downs by RNA-seq. From these data, we identified a group of RNAs that were enriched in the GsrN(37)-PP7hp fraction.
 
Overall design For Rockhopper analysis:
RNA-seq reads of three replicate GsrN(37)-PP7hp (pos) purifications and duplicate (mock) PP7hp-GsrN purifications were quantified and analyzed with Rockhopper 2.0 (Tjaden, 2015). Reads were mapped to modified Caulobacter NA1000 genome files (FASTA, PTT, RNT) where the gsrN locus was replaced with the sequence of gsrN(37)-PP7hp. We pruned the data set to find genes that had a low FDR values (“qValue” < .05), were specifically enriched in the GsrN(37)-PP7 (“Expression GsrN(37)-PP7hp” > “Expression PP7hp”), and had a high level of reads mapped to the gene in the GsrN(37)::PP7 (“Expression GsrN(37)-PP7hp” >1000).

For sliding window analysis:
Read quantification across the three independent GsrN(37)-PP7hp fractions showed some differences. In sample 1 (pos_rep1) 2.69% reads mapped to gsrN(37)-PP7hp, while 15.78% and 14.04% mapped to GsrN in samples 2 (pos_rep2) and 3 (pos_rep3) respectively. We observed several genes that were strongly enriched in sample 1 but not in sample 2 and 3. Thus we employed a metric to balance the discrepancies between the three independent purifications. To minimize potential false positives, we calculated the average of all three samples and the average of samples 2 and 3. If the total average was 1.5 times greater than the sample 2 and 3 average, we assumed that the sample 1 artificially raised the average RPKM value and did not consider any data from any of the purifications in that specific window.


 
Contributor(s) Tien MZ, Fiebig A
Citation(s) 29537368
NIH grant(s)
Grant ID Grant title Affiliation Name
R01 GM087353 Integrated Control of Caulobacter Cell Physiology by Visible Light and Stress UNIVERSITY OF CHICAGO SEAN CROSSON
U19 AI107792 Defining the functions of uncharacterized genes in priority pathogens UNIVERSITY OF CHICAGO SEAN CROSSON
Submission date Oct 25, 2017
Last update date May 15, 2019
Contact name Sean Crosson
E-mail(s) crosson4@msu.edu
Phone 5178845345
Organization name Michigan State University
Department Dept. Microbiology and Molecular Genetics
Street address 567 Wilson Rd
City East Lansing
State/province Michigan
ZIP/Postal code 48824
Country USA
 
Platforms (1)
GPL22063 Illumina HiSeq 4000 (Caulobacter vibrioides)
Samples (5)
GSM2830964 pos_rep1
GSM2830965 pos_rep2
GSM2830966 pos_rep3
Relations
BioProject PRJNA415810
SRA SRP121478

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
GSE106171_CP001340_2016_09_22_G12_SW_25_sense.ptt.txt.gz 1.1 Mb (ftp)(http) TXT
GSE106171_CP001340_2016_09_22_G12_SW_25_sense.rnt.txt.gz 244 b (ftp)(http) TXT
GSE106171_CP001340_2016_09_22_G17_SW_25_sense.ptt.txt.gz 1.1 Mb (ftp)(http) TXT
GSE106171_CP001340_2016_09_22_G17_SW_25_sense.rnt.txt.gz 243 b (ftp)(http) TXT
GSE106171_CP001340_2016_G12.fna.gz 1.2 Mb (ftp)(http) FNA
GSE106171_CP001340_2016_G17.fna.gz 1.2 Mb (ftp)(http) FNA
GSE106171_NC_999999_transcripts.txt.gz 313.5 Kb (ftp)(http) TXT
GSE106171_RAW.tar 7.6 Mb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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