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SRX1388017: GSM1919507: YTHDC1 IP Ribo(-); Homo sapiens; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 14.4M spots, 1.4G bases, 552.3Mb downloads

Submitted by: NCBI (GEO)
Study: N6-methyladenosine-Mediated Nuclear Export of Messenger RNA
show Abstracthide Abstract
N6-methyladenosine (m6A) is the most common internal modification in eukaryotic messenger RNA (mRNA). The effects of this reversible cheimcal modification are mediated in part by methyl-specific RNA binding protein ''readers'' of the YTH family. In this study we present the function of YTHDC1 (YT521) in promoting the export of mRNA from the nucleus to the cytoplasm. Additionally, we identify a role for YTHDC1 in exon retention in mouse embryonic stem cells (mESCs). Overall design: Two complementary methods were used to determine YTHDC1 target transcripts within HeLa cells. Subcellular RNA-sequencing following knockdown of YTHDC1 was used to analyze transcript distribution. In mESCs, knockout of Ythdc1 showed minor splicing differences. We analyzed the differences in RNA binding by NXF1 and SRSF3 by RIP-seq in the presence and absence of YTHDC1.
Sample: YTHDC1 IP Ribo(-)
SAMN04217916 • SRS1136119 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: PAR-CLIP was performed as previously described (Xu et al., 2014). Breifly, Flag-tagged YTHDC1 was immunoprecipitated from transfected HeLa cells and treated with Rnase. Bound RNA fragments were isolated with TriZol following Proteinase K digestion and subject to ibrary construction. RIP was performed according to literature procedure (Peritz et al., 2006) using polyA selected RNA and ribosomal RNA depleted RNA as biological replicates. HeLa cells were fractionated using NE-PER Nuclear and Cytoplasmic Extraction Reagents (Thermo Scientific) according to manufacturer protocol with the following modifications: following cytoplasmic isolation, nuclei were washed extensively (4 x 200 μL) with PBS. RNA from each portion was collected using Directzol RNA miniprep (Zymo Research) and treated with DNaseI. Samples were depleted of ribosomal RNA prior to sequencing. mESC mRNA was isolated using TriZol reagent and purified using poly-T oligo magnetic beads. PAR-CLIP libraries were constructed using Illumina TruSeq Small RNA (Rep 1) or NEBNext Small RNA (Rep 2) library construction kits. RIP-seq and subcellular RNA-seq libraries were constructed using the Illumina TruSeq Stranded mRNA kit. mESC mRNA libraries were constructed using the NEBNext Ultra Directional RNA library construction kit.
Experiment attributes:
GEO Accession: GSM1919507
Links:
Runs: 1 run, 14.4M spots, 1.4G bases, 552.3Mb
Run# of Spots# of BasesSizePublished
SRR283060314,425,7221.4G552.3Mb2017-10-16

ID:
1971739

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