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SRX19934697: GSM7163449: UAS-dTrmt10A HS m6A-IP SYS rep1; Drosophila melanogaster; OTHER
1 ILLUMINA (HiSeq X Ten) run: 23.4M spots, 7.1G bases, 2.1Gb downloads

External Id: GSM7163449_r1
Submitted by: Bonini, Biology, University of Pennsylvania
Study: The tRNA methyltransferase dTrmt10A impacts m6A levels and the stress response in the Drosophila brain
show Abstracthide Abstract
The tRNA methyltransferase TRMT10A was previously shown modulating the level of N6-methyladenosine (m6A) in polyadenylated RNA (polyA+ RNA). Here, we focus on the function of the Drosophila homolog of human TRMT10A, CG14618/dTrmt10A, and its impact on m6A regulation in the Drosophila brain and acute stress response. Using m6A-IP RNA sequencing from head tissue, we find that altering the levels of dTrmt10A modulates the levels of m6A on polyA+ RNA in the brain. Specifically, dTrmt10A affects m6A levels on transcripts enriched for signaling pathways, with a particular impact on 3' UTR m6A in response to heat shock. Furthermore, our findings indicate that upregulation of dTrmt10A results in a global decrease in m6A levels and decreases resilience to acute heat stress. Collectively, our data affirm the crucial role of m6A in the biological response of the brain to stress, and reveal that dTrmt10A acts as an additional regulator of m6A in the Drosophila brain and stress response. Overall design: head m6A-IP used to investigate the role of the m6A RNA modification in heat shock stress and dTrmt10A knockdown and upregulation.
Sample: UAS-dTrmt10A HS m6A-IP SYS rep1
SAMN34146149 • SRS17284482 • All experiments • All runs
Library:
Name: GSM7163449
Instrument: HiSeq X Ten
Strategy: OTHER
Source: TRANSCRIPTOMIC
Selection: other
Layout: PAIRED
Construction protocol: For m6A-IP seq flies were flash frozen and head tissue was collected into cold RNAse free tubes. Total RNA was extracted from 200 Drosophila Heads per replicate using Trizol/ chloroform extraction. PolyA+ mRNA was obtained using NEBNext Poly(A) mRNA Magnetic Isolation Module. PolyA+ RNA was fragmented using the NEB Next Magnesium Fragmentation Module (NEB, E6150S) for 4 minutes at 95 °C for a 250 ng sample of polyA+ RNA, and RNA was repurified using the Zymo RNA clean & concentrator -5 kit (Zymo, R1013). 10% of the fragmented polyA+ RNA was saved as an input control for sequencing. M6A -immunoprecipitation was done using the EpiMark N6-Methyladenosine Enrichment kit protocol with some minor alteration. 30ul of protein G magnetic beads (NEB, #S1430) were washed and resuspended in IP buffer (150mM NaCl, 10mM Tris-HCL, 0.1% NP-40). 4ul of synaptic systems antibody (SYS, 202003) was conjugated to protein G-magnetic beads (NEB, S1430S) for 2 hours at 4°C. Beads/ antibody were washed twice in IP buffer. ~1μg PolyA+ RNA was incubated with beads/antibody in IP buffer supplemented with 0.1% SUPERase-In RNase Inhibitor (Thermo Fisher; AM2696) for 2 hours at 4°C. After incubation, RNA/beads/antibody are washed twice in IP buffer, twice in low salt IP buffer (50mM NaCl, 10mM Tris-HCL, 0.1% NP-40), and twice in high salt IP buffer (500mM NaCl, 10mM Tris-HCL, 0.1% NP-40). RNA is eluted from beads with 25μl of RLT buffer twice and elution was pooled and concentrated using Zymo RNA clean and concentrator kit-5 (R1015). Libraries were made using SMARTer Stranded Total RNA-Seq Kit V2 without rRNA depletion(takarabio, 634411) for IPed and input RNA, and sequenced using illumina HiSeq with 40M paired end reads (2x150bp). Library preparation and sequencing was done by Admera Health. Three biological replicates per genotype and condition were done with Synaptic Systems m6A antibody. Libraries were made using SMARTer Stranded Total RNA-Seq Kit V2 without rRNA depletion (takarabio, 634411) for IPed and input RNA, sequenced using illumina HiSeq with 40M paired end reads (2x150bp).
Runs: 1 run, 23.4M spots, 7.1G bases, 2.1Gb
Run# of Spots# of BasesSizePublished
SRR2413603823,372,0177.1G2.1Gb2023-12-12

ID:
27310225

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