NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE227923 Query DataSets for GSE227923
Status Public on Oct 23, 2023
Title Transfer RNA pools in human cells are controlled by selective gene expression [ATAC-seq]
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Transfer RNAs are required for translating genetic information into protein sequence. The human genome contains hundreds of tRNA genes, many of which in multiple copies. How their expression is regulated to control functional tRNA levels is unknown. Here, we combined quantitative tRNA profiling and ChIP-Seq to measure tRNA expression upon differentiation of human induced pluripotent stem cells (hiPSC) into neuronal and cardiac cells. We find that tRNA transcript pools vary substantially, while the abundance of tRNAs with distinct anticodons, which governs decoding rates, is more stable among cell types. Mechanistically, RNA Polymerase III (Pol III) samples a wide range of tRNA genes in hiPSC and becomes constrained to a housekeeping subset upon differentiation. This is mediated by diminished mTOR signaling, which activates the Pol III repressor MAF1. Our data rationalize how tRNA anticodon pools are buffered in different cellular contexts and reveal that mTOR activity drives selective tRNA expression.
 
Overall design Human induce pluoripotent stem cells (hiPSC), and derived neural progenitors (NPC), mature neurons, and cardiomyocytes (CM) were cultured. Subsequent chromatin immunoprecipitation DNA-sequencing (ChIP-seq) for RNA Polymerase III subunit RPC1, TFIIIB subunit BRF1, histone modifications H3K4me3 and K3K27me3, ATAC-Seq, RNA-Seq, ribosome profiling followed by sequencing (Ribo-Seq) and tRNA-Seq datasets were generated to investigate the regulation of tRNA genes upon differentiation of hiPSCs.
 
Contributor(s) Gao L, Behrens A, Rodschinka G, Forcelloni S, Wani S, Strasser K, Nedialkova DD
Citation(s) 38191669
Submission date Mar 22, 2023
Last update date Jan 22, 2024
Contact name Danny Nedialkova
E-mail(s) nedialkova@biochem.mpg.de
Organization name Max Planck Institute for Biochemistry
Lab Mechanisms of Protein Biogenesis
Street address Am Klopferspitz 18
City Planegg
State/province Bayern
ZIP/Postal code 82152
Country Germany
 
Platforms (1)
GPL18573 Illumina NextSeq 500 (Homo sapiens)
Samples (8)
GSM7110999 hiPSC kucg-2 ATAC-Seq rep1
GSM7111000 hiPSC kucg-2 ATAC-Seq rep2
GSM7111001 NPC ATAC-Seq rep1
This SubSeries is part of SuperSeries:
GSE227928 Selective gene expression maintains human tRNA anticodon pools during differentiation
Relations
BioProject PRJNA947523

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE227923_ATAC-Seq_NFR_tRNAcounts.csv.gz 6.6 Kb (ftp)(http) CSV
GSE227923_RAW.tar 26.9 Mb (http)(custom) TAR (of NARROWPEAK)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap