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SRX8156863: GSM4490921: Sso-RNAseq rep1; Saccharolobus solfataricus; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 21.8M spots, 1.6G bases, 970.5Mb downloads

Submitted by: NCBI (GEO)
Study: iCLIP analysis of RNA substrates of the archaeal exosome (RNA-Seq)
show Abstracthide Abstract
In this study, an exoribonuclease was analyzed by iCLIP. The data documents the role of the archaeal exosome as an exoribonuclease and RNA-tailing enzyme interacting with all RNA classes. Mapping of most reads to mRNAs underlines the role of exosome in mRNA turnover, which is important for adaptation of prokaryotic cells to changing environmental conditions. The clustering of crosslink sites near 5'-ends of genes suggests simultaneous binding of both RNA ends by the S. solfataricus exosome. This may serve to prevent translation of mRNAs designated to degradation in 3'-5' direction. Overall design: 1 samples, 3 replicates
Sample: Sso-RNAseq rep1
SAMN14670178 • SRS6518875 • All experiments • All runs
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: The total RNA samples were first fragmented using ultrasound (4 pulses of 30 sec at 4°C). Each sample was used for three independent cDNA synthesis. First, an oligonucleotide adapter was ligated to the 3' end of the RNA molecules. First-strand cDNA synthesis was performed using M-MLV reverse transcriptase and the 3' adapter as primer. The first-strand cDNA was purified and the 5' Illumina TruSeq sequencing adapter was ligated to the 3' end of the antisense cDNA. The resulting cDNA was PCR-amplified to about 10-20 ng/μl using a high fidelity DNA polymerase. The cDNA was purified using the Agencourt AMPure XP kit (Beckman Coulter Genomics) and was analyzed by capillary electrophoresis. The total RNA samples were first fragmented using ultrasound (4 pulses of 30 sec at 4°C). Each sample was used for three independent cDNA synthesis. First, an oligonucleotide adapter was ligated to the 3' end of the RNA molecules. First-strand cDNA synthesis was performed using M-MLV reverse transcriptase and the 3' adapter as primer. The first-strand cDNA was purified and the 5' Illumina TruSeq sequencing adapter was ligated to the 3' end of the antisense cDNA. The resulting cDNA was PCR-amplified to about 10-20 ng/μl using a high fidelity DNA polymerase. The cDNA was purified using the Agencourt AMPure XP kit (Beckman Coulter Genomics) and was analyzed by capillary electrophoresis.
Experiment attributes:
GEO Accession: GSM4490921
Links:
Runs: 1 run, 21.8M spots, 1.6G bases, 970.5Mb
Run# of Spots# of BasesSizePublished
SRR1158950921,798,9481.6G970.5Mb2020-11-25

ID:
10634096

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