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SRX11661853: GSM5506302: Ribo-seq frq knockout DD40 rep2; Neurospora crassa; OTHER
1 ILLUMINA (Illumina HiSeq 3000) run: 66.2M spots, 3.4G bases, 1Gb downloads

Submitted by: NCBI (GEO)
Study: Circadian Clock-Controlled Translation of Specific mRNAs in Neurospora crassa Requires Rhythmic eIF2a Activity and P-body Sequestration [Ribo-seq]
show Abstracthide Abstract
We report the genome-wide impact of rhythmic P-eIF2a levels in vivo by performing ribosome profiling and RNA-seq in Neurospora crassa samples grown over a circadian time course. We identified candidate genes which showed rhyhmic ribosome occupancy in WT cells but lost rhythms in mRNA levels and ribosome occupancy in the clock mutant Dfrq, eIF2a kinase knockout Dcpc-3, and constitutively active kinase mutant cpc-3c cells. Select mRNAs harbor a P-body localization motif identified by MEME and MEME Suite's GOMo function. P-body localization of the target mRNAs provides an attractive mechanism for explaining translational rhythms from otherwise arrhythmic mRNAs. Overall design: Ribosome profiling (ribo-seq) (done in parallel with RNA-seq) of Neurospora crassa WT, clock mutant Dfrq, eIF2a kinase knockout Dcpc-3, and constitutively active kinase mutant cpc-3c mycelia, grown over a circadian time course. Each time point has a duplicate.
Sample: Ribo-seq frq knockout DD40 rep2
SAMN20601195 • SRS9694679 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 3000
Strategy: OTHER
Source: TRANSCRIPTOMIC
Selection: other
Layout: SINGLE
Construction protocol: Tissue was harvested in the dark, pressed in between paper towels to remove excess media, and immediately frozen in liquid N2. Ribosomes were pelleted by sucrose-density centrifugation and ribosome-protected mRNAs were isolated from the pelleted cell extracts using the Qiagen miRNeasy Mini Kit (Cat. # 217004). All subsequent steps up to step 46 in the published ribosome profiling protocol (Ingolia et al., 2012) were followed as described. An rRNA depletion step was not performed, but instead after heat-inactivation of CircLigase, 2.0 μL of GlycoBlueTM, 6.0 μL 5 M NaCl, 74 μL of DEPC water, and 150 μL of isopropanol were added to each tube and precipitation was carried out overnight at -80°C. The DNA was pelleted by centrifugation for 30 min at 20,000 g at 4°C. The pellets were washed with 70% ethanol and allowed to air-dry for 10 min. The pellet was then resuspended in 5.0 μL of 10 mM Tris (pH 8.0), and cDNA synthesis using SuperScript™ III Reverse Transcriptase, followed by barcode addition by PCR amplification using Phusion Hot Start High-Fidelity DNA Polymerase were performed as described (101). Sequencing libraries were quantified and checked for quality on a 2100 Bioanalyzer using a DNA high sensitivity chip per the manufacturer's instructions.
Experiment attributes:
GEO Accession: GSM5506302
Links:
Runs: 1 run, 66.2M spots, 3.4G bases, 1Gb
Run# of Spots# of BasesSizePublished
SRR1535936766,225,2813.4G1Gb2022-11-10

ID:
15577789

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