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SRX23639954: Gst70-Ps20_2
1 ILLUMINA (Illumina MiSeq) run: 1M spots, 101.2M bases, 42.3Mb downloads

Design: In the first step, adenylation of the 3-protected RNA adapter was performed using TS2126 ligase (CircLigase). Subsequently, this adapter was ligated to the 3-end of the native tRNAs using T4Rnl2KQ. The adapter introduced the index primer binding site and served as a binding site for the reverse transcription primer. The reverse transcription primer is modified with two hexa-ethylene glycol groups that prevent rolling circle amplification during final PCR. The reverse transcription primer is used to introduce the binding site for the sequencing primer. This was followed by reverse transcription, degradation of the RNA by increasing the pH, and size selection of the cDNA using PAA gels. The cDNA was then circularized and served as a template in the final PCR. The primers used here introduced both the Illumina Flowcell sequences P5 and P7 and one of 25 6 bp i7 indices into the library. After PCR, the libraries were purified using the QIAquick PCR Purification Kit.
Submitted by: Helmholtz Institute for Metabolic, Obesity and Vascular Research (HI-MAG)
Study: RNA sequencing of tRNA libraries from 4 Bacillales, either untreated or treated with CMCT or NaBH4
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Single-end RNA sequencing (1x100 bp) was conducted on highly enriched tRNAs using an Illumina MiSeq with the MiSeq Reagent Kit v3. The tRNA libraries underwent chemical sodium borohydride (NaBH4) treatment to detect dihydrouridine, 4-thiouridine, and 7-methyl-guanosine tRNA modifications in the mapping profile, indicated by an increased occurrence of apparent read terminations compared to untreated control samples. For profiling pseudouridine, sodium borohydride 1-cyclohexyl-(2-morpholinoethyl)carbodiimide metho-p-toluene sulfonate (CMCT) treated tRNA libraries were utilized.The experiment aimed to investigate tRNA-dependent temperature adaptation mechanisms in closely related psychrophilic (Planococcus halocryophilus and Exiguobacterium sibiricum), mesophilic (Bacillus subtilis), and thermophilic (Geobacillus stearothermophilus) Bacillales. Cultures were grown at different temperatures ranging from 10 to 70C, representing optimal growth temperature as well as minimum and maximum feasible temperatures in the laboratory for each species: P. halocryophilus (10C, 20C, and 30C), E. sibiricum (10C, 20C, and 30C), B. subtilis (20C, 30C, and 37C), and G. stearothermophilus (40C, 55C, and 70C).Each NaBH4- and CMCT-treated sample, as well as the corresponding untreated negative control for each bacterium at each cultured temperature, underwent three biological replicates for a total of 36 RNA seq libraries per species.
Sample:
SAMN39960157 • SRS20475126 • All experiments • All runs
Library:
Name: 107
Instrument: Illumina MiSeq
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: PCR
Layout: SINGLE
Runs: 1 run, 1M spots, 101.2M bases, 42.3Mb
Run# of Spots# of BasesSizePublished
SRR279868591,012,301101.2M42.3Mb2024-04-02

ID:
31917686

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