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Status |
Public on Jun 22, 2020 |
Title |
Control of gene expression mRNA N6-methyladenosine in pro-B cells |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing Methylation profiling by high throughput sequencing Other
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Summary |
N6-methyladenosine (m6A) is the most abundant internal modification in eukaryotic messenger RNA (mRNA). In mice, loss of METTL14, the key m6A writer component, severely blocks B cell development. In this group of RNA sequencing data, we 1. conducted RNA-seq on WT and METTL14 KO pro-B cells (sample 1-10); 2. performed m6A-seq in WT pro-B cells (sample 11-14) and 3. conducted YTHDF2 RIP -seq in WT pro-B cells (sample 15-18). Our data supported that m6A repressed a group of genes in pro-B cells via its reader YTHDF2.
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Overall design |
Pro-B cells were sorted as CD19+B220midCD2-CD43hismallIg(kappa)/Ig(lambda)- cells from mice and subject to sequencing as described in summary.
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Contributor(s) |
Yu X, He C, Zheng Z |
Citation(s) |
32610122 |
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Submission date |
May 22, 2020 |
Last update date |
Jul 06, 2020 |
Contact name |
Chuan He |
E-mail(s) |
chuanhe@uchicago.edu
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Organization name |
University of Chicago
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Department |
Chemistry
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Street address |
929 E 57th Street
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City |
Chicago |
State/province |
IL |
ZIP/Postal code |
60637 |
Country |
USA |
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Platforms (1) |
GPL13112 |
Illumina HiSeq 2000 (Mus musculus) |
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Samples (18)
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Relations |
BioProject |
PRJNA634546 |
SRA |
SRP262999 |