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SRX5723322: GSM3732955: mRNA-seq-WT-replicate_1; Neurospora crassa; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 41.3M spots, 12.5G bases, 3.6Gb downloads

Submitted by: NCBI (GEO)
Study: Effect of adat2 silencing in Neurospora crassa on translation kinetics and transcriptome
show Abstracthide Abstract
The silencing of tRNA-specific adenosine deaminase adat2 in Neurospora crassa abolished most of the I34 modification, resulting in major tRNA profile changes. The adat2 silencing caused genome-wide codon usage-biased ribosome pausing on mRNAs corresponding to changes in the tRNA profile, which reprograms translation elongation kinetics on ADAT-related codons. The ribosome profiling in this study was used to measure the effect of defective I34 modification of the eight tRNAs on translation kinetics during elongation stage. The accompanying mRNA-seq was used to normalize the ribosome profiling data using the same library construction protocol (reference to ARTseq™ Ribosome Profiling Kit (Catalog Number: RPYSC12116)) under the same growth condition. The independent mRNA-seq was used to measure the effect of I34 abolishment on transcriptome change using standard Illumina protocols. Meanwhile, to isolate the role of codon usage in translation elongation and protein level changes when adat2 is silenced, the independent mRNA-seq was also used to exclude the effect of mRNA level changes. Overall design: The transcription profile and ribosome protected fragment (RPF) profiles of wild-type strain and adat2-silenced mutant of Neurospora crassa were generated by deep sequencing using Illumina sequencing platform.
Sample: mRNA-seq-WT-replicate_1
SAMN11477781 • SRS4661479 • All experiments • All runs
Library:
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: For the ribosome profiling and accompanying mRNA-seq, the ribosome protected fragments (RPFs) and total RNAs were extracted according to ARTseq™ Ribosome Profiling Kit(Catalog Number: RPYSC12116). For the independent mRNA-seq, total RNA was extracted using Trizol reagents (Invitrogen) and treated with DNase (Turbo DNase, Ambion) accoding to standard RNA extraction protocal. For the ribosomal profiling and the accompanying mRNA-seq, libraries were prepared for sequencing according to ARTseq™ Ribosome Profiling Kit(Catalog Number: RPYSC12116). For the independent mRNA-seq, libraries were constucted using Illumina TruSeq reagents. All RNA libraries were prepared for sequencing using standard Illumina protocols.
Experiment attributes:
GEO Accession: GSM3732955
Links:
Runs: 1 run, 41.3M spots, 12.5G bases, 3.6Gb
Run# of Spots# of BasesSizePublished
SRR900296541,295,55412.5G3.6Gb2020-05-22

ID:
7706277

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