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ERX9855564: Illumina NovaSeq 6000 sequencing; Translation Complex Profiling analysed using sequencing (TCP-seq) applied to fission yeast cells (Schizosaccharomyces pombe)
1 ILLUMINA (Illumina NovaSeq 6000) run: 15.1M spots, 1.5G bases, 437.5Mb downloads

Design: Translation Complex Profiling analysed using sequencing (TCP-seq) applied to fission yeast cells (Schizosaccharomyces pombe)
Submitted by: DEPARTMENT OF BIOCHEMISTRY UNIVERSITY OF CAMBRIDGE
Study: Translation Complex Profiling analysed using sequencing (TCP-seq) applied to fission yeast cells (Schizosaccharomyces pombe)
show Abstracthide Abstract
Translation complexes are stabilised in vivo using formaldehyde. Cells are lysed, and cell extracts are treated with RNase I to produce protected RNA fragments (FPs or footprints). Extracts are then run through sucrose gradients to separate small ribosomal subunits and full ribosomes. FPs are isolated from each of these fractions and analysed by sequencing. Note this is a modified version of ribo-seq (a.k.a. ribosome profiling)
Sample: untreated.rep3.ribo.80s.libA
SAMEA111452420 • ERS13545818 • All experiments • All runs
Library:
Name: untreated.rep3.ribo.80s.libA_s
Instrument: Illumina NovaSeq 6000
Strategy: OTHER
Source: TRANSCRIPTOMIC
Selection: other
Layout: SINGLE
Construction protocol: Cells were treated with 3% PFA for 10 min, quenched with glycine and pelleted Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (25 mM Hepes-KOH pH 7.6, 100 mM KCl, 2 mM MgCl2, 0.25% triton-100, 0.5 mM DTT, 250 mM glycine, Complete Mini EDTA Free Protease Inhibitor Cocktail (Roche), 10 mM PMSF, 100 µg/mL cycloheximide, 100 U Ribolock RNase inhibitor (ThermoFisher), and 1 U TURBO DNase (ThermoFisher)) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 5G bead-beater (MP Biomedicals) at level 7 for 13 seconds. The extract was diluted with 200 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (10 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 325 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 7.5-30% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 4 hr at 37,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing 40S and 80S complexes were selected for further processing. RNAs were then purified by phenol extraction at 65C for 45 min, and run on 10% TBE-urea gels (Life Technologies). Fragments of 15-100 nucleotides were extracted from the gel Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris pH 7, 50 mM DTT, 100 mM MgCl2) for 30 min at 37C. ATP and buffer A (Thermo Fisher) were then added for an additional 30 min incubation. RNA fragments were column-purified (PureLink RNA micro-columns, Life Technologies). 100 ng were used as input for the NEXTflex Small RNA Sequencing Kit v3 (Bioo Scientific), following manufacturer's no size selection protocol.
Experiment attributes:
Experimental Factor: compound: none
Experimental Factor: fraction: 80s
Experimental Factor: protocol: TCP-seq
Runs: 1 run, 15.1M spots, 1.5G bases, 437.5Mb
Run# of Spots# of BasesSizePublished
ERR1032321015,060,4741.5G437.5Mb2023-01-22

ID:
26328460

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