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Status |
Public on Jun 01, 2024 |
Title |
Mettl3-dependent m6A modification is essential for effector differentiation and memory formation of CD8+ T cells [miCLIP] |
Organism |
Mus musculus |
Experiment type |
Other
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Summary |
The goal of this study is to determine the critical requirement of N6-Methyladenosine (m6A) methyltransferase Mettl3 during CD8+ T cell responses upon acute viral infection. We demonstrate that conditional ablation of Mettl3 in CD8+ T cells impairs effector expansion and terminal differentiation in an m6A-dependent manner, which in turn affects memory formation and secondary response. Mechanism analysis indicates that Mettl3 deficiency broadly affects expression of cell cycle and transcriptional regulators. Based on these findings, our study reveals the important role of m6A modification in CD8+ T cell responses.
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Overall design |
Control and Mettl3ΔGzmb effector (CD44+CD62L-EYFP+) CD8+ T cells (2 samples per group) were sorted
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Citation missing |
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Submission date |
Oct 14, 2022 |
Last update date |
Jun 01, 2024 |
Contact name |
Shuyang Yu |
E-mail(s) |
ysy@cau.edu.cn
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Organization name |
China Agricultural University
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Department |
College of Biological Sciences
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Street address |
2 Yuanmingyuan West Road
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City |
Beijing |
ZIP/Postal code |
100193 |
Country |
China |
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Platforms (1) |
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Samples (8)
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This SubSeries is part of SuperSeries: |
GSE215762 |
Mettl3-dependent m6A modification is essential for effector differentiation and memory formation of CD8+ T cells |
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Relations |
BioProject |
PRJNA890578 |