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Status |
Public on Jul 20, 2017 |
Title |
Genome-wide maps of Bcl11b bound regions in thymocytes |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
T-cell receptor (TCR) signals play a critical role in guiding selected thymocytes to distinct lineages by activating genes for transcription factors, such as ThPOK and Runx3, for the helper- or cytotoxic-lineage, respectively. Here we show that Bcl11b, known as an early T-lineage commitment factor, is essential for proper expression of ThPOK and Runx3. Loss of Bcl11b resulted in premature and random expression of these specification factors, leading to lineage scrambling that was disconnected from TCR restriction by MHC. Early Thpok repression by Bcl11b is independent of its known transcriptional silencer, but requires the C-terminal zinc-finger of Bcl11b. Collectively, our findings shed new light on the role of Bcl11b in priming lineage-specifying genes to integrate TCR signals into a subsequent developmental program that dissects effector lineages.
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Overall design |
Sequencing of Bcl11b ChIP-seq from thymocytes.
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Contributor(s) |
Taniuchi I, Kojo S, Endo TA |
Citation(s) |
28951542 |
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Submission date |
Dec 06, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Takaho A. Endo |
E-mail(s) |
takaho.endo@riken.jp
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Organization name |
RIKEN
|
Department |
IMS
|
Lab |
Laboratory for Integrative Genomics
|
Street address |
1-7-22 Suehiro, Tsurumi
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City |
Yokohama |
State/province |
Kanagawa |
ZIP/Postal code |
230-0045 |
Country |
Japan |
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Platforms (1) |
GPL18480 |
Illumina HiSeq 1500 (Mus musculus) |
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Samples (2) |
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This SubSeries is part of SuperSeries: |
GSE90990 |
Bcl11b hypomorphic mutant thymocytes |
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Relations |
BioProject |
PRJNA356425 |
SRA |
SRP094644 |