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Status |
Public on May 03, 2013 |
Title |
Whole genome mRNA analysis of wild-type and Id2-deficient virus-specific CD8+ T cells after influenza infection |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
The transcription factor Inhibitor of DNA binding 2 (Id2) modulates T cell fate decisions but the molecular mechanism underpinning this regulation is unclear. Here, using whole genome mRNA analysis we show that loss of Id2 programs CD8+ T cells to adopt a memory fate with increased Eomesodermin and Tcf7 expression. Our findings reveal that the Id2-E2A axis orchestrates T cell differentiation through the induction or repression of downstream transcription factors essential for effector and memory T cell differentiation.
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Overall design |
Wild-type and Id2fl/flLckCre+ DbNP366-specific CD8+ T cells were isolated from the spleen of PR8-primed/HKx31-infected Ly5.2+Id2fl/flLckCre+:Ly5.1+ mixed bone marrow chimeric mice ten days after intranasal influenza infection and analysed by whole genome mRNA analysis. Three biological replicates of each genotype were subjected to microarray analysis.
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Contributor(s) |
Masson F, Belz GT |
Citation(s) |
23536629, 24723679 |
Submission date |
Feb 07, 2013 |
Last update date |
Jan 16, 2019 |
Contact name |
Moshe Olshansky |
E-mail(s) |
olshansky@wehi.edu.au
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Organization name |
Walter & Eliza Hall Institute of Medical Research
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Department |
Bioinformatics
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Lab |
Speed
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Street address |
1G Royal Pde
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City |
Parkville |
State/province |
Victoria |
ZIP/Postal code |
3052 |
Country |
Australia |
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Platforms (1) |
GPL6887 |
Illumina MouseWG-6 v2.0 expression beadchip |
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Samples (6)
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Relations |
BioProject |
PRJNA188770 |