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Series GSE151704 Query DataSets for GSE151704
Status Public on May 05, 2022
Title FTO mediates LINE1 m6A demethylation and chromatin regulation in mESCs and mouse tissues
Organism Mus musculus
Experiment type Other
Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Summary N6-methyladenosine (m6A) is the most abundant internal modification in mammalian messenger RNA (mRNA). It is installed by writer proteins and can be reversed by erasers. FTO was the first RNA demethylase shown to catalyze oxidative demethylation of m6A in RNA. Despite extensive studies, the main physiological substrates of FTO and the related functional pathways remain elusive in many systems, in particular during early mammalian development. Here, we show that FTO mediates the m6A demethylation of chromosome-associated repeat RNAs in mouse embryonic stem cells (mESCs), especially the long-interspersed element-1 family (LINE1) RNA, thereby affecting their abundances to regulate chromatin state.
 
Overall design ChIP profiles of histone marks and transcription factors in WT and Fto knockout mESCs were generated by deep sequencing, in duplicate using Illumina NovaSeq 6000. Nuclear RNA lifetime and nascent RNA synthesis of WT and Fto knockout mESCs were generated by deep sequencing, in triplicate, using Illumina NovaSeq 6000 machine.Embryos at GV, MII and morula stages were transferred to 500 ?l Trizol Reagent and then mixed well with 100 ?l chloroform added. The mixture was transferred Qiagen MaXtract High Density tubes (129046). After centrifuge, upper and aqueous phase was removed. RNA was precipitated by adding equal volume isopropanol and washing by 75% ethanol. Then purified RNA were analyzed by RT-qPCR or subjected to library generation using SMARTer Stranded Total RNASeq Kit (Takara Bio) following manufacturer?s protocol. Libraries were sequenced on an Illumina NovaSeq 6000 platform in paired-end read mode with 150 bp per read.
ATAC-Seq was performed on wild-type and FTO knockout mESCs.
Web link https://pubmed.ncbi.nlm.nih.gov/35511947/
 
Contributor(s) Yu X, Wei J, He C
Citation(s) 35511947
Submission date Jun 03, 2020
Last update date Aug 04, 2022
Contact name Chuan He
E-mail(s) chuanhe@uchicago.edu
Organization name University of Chicago
Department Chemistry
Street address 929 E 57th Street
City Chicago
State/province IL
ZIP/Postal code 60637
Country USA
 
Platforms (2)
GPL13112 Illumina HiSeq 2000 (Mus musculus)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
Samples (104)
GSM4588521 mESC_caRNA_m6A_FtoKO_rep1_IP
GSM4588522 mESC_caRNA_m6A_FtoKO_rep1_Input
GSM4588523 mESC_caRNA_m6A_FtoKO_rep2_IP
Relations
BioProject PRJNA637027
SRA SRP265795

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
GSE151704_RAW.tar 30.2 Mb (http)(custom) TAR (of NARROWPEAK, TXT)
GSE151704_count.gene.EU.csv.gz 4.4 Mb (ftp)(http) CSV
GSE151704_count.gene.GV.csv.gz 3.9 Mb (ftp)(http) CSV
GSE151704_count.gene.MII_Molura.csv.gz 4.1 Mb (ftp)(http) CSV
GSE151704_count.gene.lifetime.csv.gz 4.1 Mb (ftp)(http) CSV
GSE151704_mESC_KO.narrowPeak.gz 2.7 Mb (ftp)(http) NARROWPEAK
GSE151704_mESC_WT.narrowPeak.gz 2.7 Mb (ftp)(http) NARROWPEAK
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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