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Status |
Public on Oct 03, 2022 |
Title |
8325-4phi13kan, + Mitomycin C, Rep 2 [5-8325-4DF-phi-13Kana-delta-rep_PSS] |
Sample type |
SRA |
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Source name |
8325
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Organism |
Staphylococcus aureus |
Characteristics |
strain: 8325 variant: single-lysogen prophage: phi13kana-Δrep treatment: mitomycin C treated
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Treatment protocol |
Samples were treated by induction with mitomycin C (300 ng/ml) or without treatment of mitomycin C as a control for 1 h. Each strain and condition was performed in biological triplicates
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Growth protocol |
Samples of 8325-4phi13kana and MW2cphi13kana were grown to OD600 = 0.7 (late exponential growth phase) at 37°C,200 rpm in TSB.
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Extracted molecule |
total RNA |
Extraction protocol |
Bacterial pellets were resuspended in TRIzol (Thermo Fisher Scientific) and mechanically lysed using zirconia/silica beads in a high speed homogenizer. RNA was further purified using the ExpressArt® RNA ready Add-on Kit for TRIzol extraction (AmpTec) with the following modifications. After loading the sample on an RNAready column, RNA was washed additionally with inhibitor removal buffer (5 M guanidine-HCl, 20 mM Tris-HCl pH 6.6, 37 % (v/v) EtOH). DNase digest of the sample was directly performed on the column. Library preparation on rRNA depleted RNA samples was performed as follows: first Illumina TruSeq sequencing adapter (CTGAAGCT) was ligated to RNAs containing a 5´monophosphate end (resulting from processing events and thereby represent PSS) followed by treatment with TEX (Terminator Exonuclease, Lucigen) to remove unligated 5´P-ends. Next, RNA 5´Polyphosphatase (5´PP, Lucigen) was used to convert triphosphate groups at 5´-RNA ends to monophosphate 5´-RNA ends. Formed monophosphate ends were then tagged by ligation of a second Illumina TruSeq sequencing adapter (TAATGCGC) (representing TSS). After fragmentation, an oligonucleotide adapter was ligated to the 3´ end of RNA fragments and cDNA synthesis performed using M-MLV reverse transcriptase. cDNA was PCR amplified within 16 cycles using high fidelity DNA polymerase. cDNA was purified using Agencourt AMPure XP Kit (Beckman Coulter Genomics)
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
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Description |
5´P Íllumina TruSeq sequencing tag CTGAAGCT to enrich PSS before TEX-treatment
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Data processing |
library strategy: tagRNA-seq CLC Genomics Workbench 20.0.3 Sequence reads were trimmed for adaptor sequence list using CLC genomic benchwork (parameter- Quality trim = yes / Quality limit: 0.05 / PolyA-tail <10) Trimmed sequence reads were mapped 8325-4phi13Kana or MW2cphi13Kana genomic sequence using CLC genomic benchwork (mismath cost: 2; insertion cost: 3; deletion cost: 3; length fraction: 0.8; similarity fraction: 0.8) Read count extraction and normalization (of unassigned (trimmed)-files) resulting in RPKM values were performed using CLC genomic benchwork Transcriptional start site prediction was performed with TSS.fastq.gz-files as the enriched libraries and PSS.fastq.gz-files as control normal libraries using TSSpredator. A detailed description of TSSpredator parameters, TSS classes and output files can be taken from the UserManual available at: http://it.inf.uni-tuebingen.de/?page_id=190. Assembly: NCBI ID: S. aureus NCTC 8325: NC_007795.1; S. aureus MW2: NC_003923.1, both strains were manually phagecured and phi13 prophage sequence inserted manually into hlb gene Supplementary files format and content: txt format files (GE): RPKM values calculated from unassigned (trimmed)-data
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Submission date |
Sep 30, 2022 |
Last update date |
Oct 03, 2022 |
Contact name |
Christiane Wolz |
E-mail(s) |
christiane.wolz@uni-tuebingen.de
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Organization name |
University Tübingen
|
Street address |
Elfriede-Aulhorn-Strasse 6
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City |
Tübingen |
ZIP/Postal code |
72076 |
Country |
Germany |
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Platform ID |
GPL24034 |
Series (1) |
GSE214523 |
Influence of Staphylococcus aureus strain background on Sa3 phage life cycle switches |
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Relations |
BioSample |
SAMN31104832 |
SRA |
SRX17761072 |