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GEO help: Mouse over screen elements for information. |
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| Status |
Public on Jul 18, 2014 |
| Title |
High-resolution mapping reveals a conserved, widespread, dynamic meiotically regulated mRNA methylation program [Mm] |
| Organism |
Mus musculus |
| Experiment type |
Other
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| Summary |
N6-methyladenosine (m6A) is a common modification of mRNA, with potential roles in fine-tuning the RNA life cycle, but little is known about the pathways regulating this process and its physiological role. Here, we used mass-spectrometry to identify a dense network of proteins physically interacting with METTL3, a core component of the methyltransferase complex, and show that two of them, WTAP and KIAA1429, are required for methylation. Combining high resolution m6A-Seq with knockdown of WTAP allowed us to define accurate maps, at near single-nucleotide resolution, of sites of mRNA methylation across four dynamic programs in human and mouse, including development, differentiation, reprogramming and immune response. Internal WTAP-dependent methylation sites were largely static across the different surveyed conditions and present in the majority of mRNAs. However, methylations were found at much lower levels within highly expressed mRNAs, and methylation is inversely correlated with mRNA stability, consistent with a role in establishing an overall basal, cell-type invariant, distribution of degradation rates. In addition, we identify thousands of WTAP-independent methylation sites at transcription initiation sites, forming part of the mRNA cap structure. We show that the methylations occur at the first transcribed nucleotide, and find that thousands of transcripts are present in different isoforms differing in the methylation state of the first transcribed nucleotide, a previously unappreciated complexity of the transcriptome. Together, our data sheds new light on the proteomic and transcriptional underpinnings of this epitranscriptomic modification in mammals.
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| Overall design |
Examination of m6A methylation across different knockdowns using shRNAs in mouse embryonic fibroblasts, in embyronic and adult brains, and in dendritic cell stimulated with LPS.
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| Contributor(s) |
Schwartz S, Maxwell M, Lander ES, Regev A |
| Citation(s) |
24981863 |
| Submission date |
Mar 04, 2014 |
| Last update date |
May 15, 2019 |
| Contact name |
Schraga Schwartz |
| Organization name |
WEIZMANN INSTITUTE OF SCIENCE
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| Street address |
Herzl 234, Department of Molecular Genetics
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| City |
Rehovot |
| State/province |
Choose a State or Province |
| ZIP/Postal code |
7610001 |
| Country |
Israel |
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| Platforms (2) |
| GPL13112 |
Illumina HiSeq 2000 (Mus musculus) |
| GPL17021 |
Illumina HiSeq 2500 (Mus musculus) |
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| Samples (26)
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| This SubSeries is part of SuperSeries: |
| GSE54365 |
High-resolution mapping reveals a conserved, widespread, dynamic meiotically regulated mRNA methylation program |
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| Relations |
| BioProject |
PRJNA240094 |
| SRA |
SRP039402 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE55575_RAW.tar |
2.4 Gb |
(http)(custom) |
TAR (of BED, TDF) |
SRA Run Selector |
| Raw data are available in SRA |
| Processed data provided as supplementary file |
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