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Status |
Public on Aug 18, 2013 |
Title |
Global DNA Methylation Remodeling Accompanies CD8 T Cell Effector Function |
Organism |
Mus musculus |
Experiment type |
Methylation profiling by high throughput sequencing
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Summary |
In response to acute infection CD8 T cells differentiate into effector cells capable of clearing the antigen. While the transcriptional and functional changes have previously been studied little is known of the epigenetic modifications that accompany this differentiation process. To gain insights into CD8 T cell effector differentiation and the role of epigenetics, we mapped DNA methylation by MeDIP-seq in naive CD8 T cells and day 8 effector CD8 T cells that are induced following an acute infection. We identified hundreds of thousands of differentially methylated regions (DMRs). Promoter DNA methylation inversely correlated with gene expression and DMRs were enriched for functional transcription factor binding sites. These data indicated that DNA methylation is dynamic during CD8 T cell differentiation and provide a map of possible regulatory regions important in this process.
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Overall design |
Examination of DNA methylation during CD8 T cell differentiation from naïve to day 8 effectors following acute infection
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Contributor(s) |
Scharer CD, Boss JM |
Citation(s) |
23956425 |
Submission date |
Feb 25, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Chris Scharer |
E-mail(s) |
cdschar@emory.edu
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Organization name |
Emory University
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Department |
Microbiology and Immunology
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Lab |
Chris Scharer
|
Street address |
1510 Clifton Rd, Suite 3086A
|
City |
Atlanta |
State/province |
GA |
ZIP/Postal code |
30322 |
Country |
USA |
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Platforms (1) |
GPL13112 |
Illumina HiSeq 2000 (Mus musculus) |
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Samples (3) |
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Relations |
SRA |
SRP018844 |
BioProject |
PRJNA191093 |