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SRX24925768: GSM8328968: h- 972 cells, wild type, minimal medium w/o nitrogen 4 hrs, rep 2; Schizosaccharomyces pombe; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 19.4M spots, 5.8G bases, 1.9Gb downloads

External Id: GSM8328968_r1
Submitted by: https://ibfg.usal-csic.es/sergio-moreno.html, IBFG, Institute of Functional Biology and Genomics (IBFG) (CSIC)
Study: The Greatwall-Endosulfine-PP2A/B55 pathway controls entry into quiescence by promoting translation of Elongator-tuneable transcripts
show Abstracthide Abstract
Here, we report that the Greatwall-Endosulfine-PPA/B55 pathway connects the downregulation of TORC1 with the upregulation of TORC2, resulting in the activation of Elongator-dependent tRNA modifications essential for sustaining the translation programme during entry into quiescence. This process promotesU34 and A37 tRNA modifications at the anticodon stem loop, enhancing translation efficiency and fidelity of mRNAs enriched for AAA versus AAG lysine codons. Notably, some of these mRNAs encode inhibitors of TORC1, activators of TORC2, tRNA modifiers, and proteins necessary for telomeric and subtelomeric functions. Therefore, we propose a novel mechanism by which cells respond to nitrogen stress at the level of translation, involving a coordinated interplay between the tRNA epitranscriptome and biased codon usage. Overall design: We performed a comparative gene expression profiling analysis of RNA-seq data between wild type cells and the mutants igo1? and nmt41:GST:pab1+ igo1? growing in minimal medium lacking nitrogen (MM-N) after 4 hours .
Sample: h- 972 cells, wild type, minimal medium w/o nitrogen 4 hrs, rep 2
SAMN41834022 • SRS21631035 • All experiments • All runs
Library:
Name: GSM8328968
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Cells were washed with cold DEPC-H2O and snap freeze. RNA extraction was carried out by disrupting the cells with cells with glass beads in TRIzol® Reagent (Invitrogen) and following the manufacturer's instructions. Library preparation using the Illumina TruSeq Stranded Total RNA and subsequent NGS sequencing was performed by Macrogen.
Runs: 1 run, 19.4M spots, 5.8G bases, 1.9Gb
Run# of Spots# of BasesSizePublished
SRR2941232419,358,9885.8G1.9Gb2024-06-17

ID:
33262011

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