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SRX8465980: GSM4589667: B6J_3_batch1_forebrain_RNA; Mus musculus; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 25.9M spots, 5.2G bases, 3.1Gb downloads

Submitted by: NCBI (GEO)
Study: Expression of the neuronal tRNA n-Tr20 regulates synaptic transmission and seizure susceptibility
show Abstracthide Abstract
Loss of the nuclear-encoded brain-specific arginine UCU tRNA, n-Tr20, gene increases seizure threshold in mice, and alters inhibitory neurotransmission in the hippocampus. We investigated the molecular impact of loss of n-Tr20 expression on the trancriptome and translatome in the forebrain and hippocampus of multiple n-Tr20 mutant and control strains. Loss of n-Tr20 altered translation initiation by activating the integrated stress response and suppressing mTOR signaling, the latter of which contributes to the enhanced GABAergic transmission. Overall design: 33 samples are analyzed in this study from n-Tr20 tRNA knockouts and transgenes in the context of C57BL/6J (B6J) and C57BL6/NJ (B6N) forebrain and hippocampus. The design includes 4 replicates each of forebrain RNA-seq from B6N, B6N-nTr20-/-, B6J-nTr20-/-, B6J, and B6J with the B6N n-Tr20 transgene (B6J-Tg(nTr20N/N) or B6J-Tgwt) mice; one sample was sequenced twice to account for batch effects. Additionally, this study includes hippocampus RNA-seq and ribosome profiling with 3 replicates each from B6N and B6N-nTr20-/- hippocampi.
Sample: B6J_3_batch1_forebrain_RNA
SAMN15096369 • SRS6767199 • All experiments • All runs
Organism: Mus musculus
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: For forebrain samples, forebrains were isolated, and stored in RNAlater and frozen at -20C. Following ribosomal RNA depletion, the remaining RNA was purified, fragmented, and libraries were prepared using TruSeq Stranded Total RNA with RiboZero-Mouse (Illumina). mRNA libraries for the assessment of translational efficiency in the B6JN and B6JN-nTr20-/- hippocampus were prepared using the TruSeq v2 mRNA kit (Illumina). mRNA was purified using biotin-tagged polydT oligonucleotides and streptavidin-coated magnetic beads. Ribosome profiling libraries were generated from B6N and B6N-nTr20-/- hippocampi. Libraries were constructed as previously described (Ingolia et al., 2012) RNA libraries were prepared for sequencing using standard Illumina protocols and ribosome profiling libraries were prepared following the protocol described in Ingolia et al., 2012
Experiment attributes:
GEO Accession: GSM4589667
Links:
Runs: 1 run, 25.9M spots, 5.2G bases, 3.1Gb
Run# of Spots# of BasesSizePublished
SRR1191958525,923,7765.2G3.1Gb2020-06-04

ID:
11005661

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