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Status |
Public on Sep 01, 2015 |
Title |
The microRNA-212/132 cluster regulates B cell development and apoptosis by targeting SOX4 |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
MicroRNAs have emerged as key regulators of B cell fate decisions and immune function. Deregulation of several microRNAs in B cells leads to the development of autoimmune disease and cancer in mice. We demonstrate that the microRNA-212/132 cluster (miR-212/132) is induced in B cells in response to B cell receptor signaling. Enforced expression of miR-132 results in a block in early B cell development at the pre-pro-B cell to pro-B cell transition and induces apoptosis in primary bone marrow B cells. Importantly, loss of miR-212/132 results in increased B cell output under non-homeostatic conditions. We find that miR-212/132 regulates B lymphopoiesis by targeting the transcription factor SOX4. Co-expression of SOX4 with miR-132 rescues the defect in B cell development from over-expression of miR-132 alone. In addition, we show that the expression of miR-132 in cells that are prone to spontaneous B cell cancers can have a protective effect on cancer development. We have thus uncovered a novel regulator of B cell lineage specification that may potential applications in B cell cancer therapy
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Overall design |
RNA-seq of wild-type and microRNA-212/132 knock-out B-cells after IgM stimulation
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Contributor(s) |
Mehta A, Marinov GK, Baltimore D |
Citation(s) |
26371188 |
Submission date |
Mar 13, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Georgi Kolev Marinov |
Organization name |
STANFORD UNIVERSITY
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Department |
Genetics
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Street address |
279 Campus Drive West, Beckman Center, B-257A/259
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City |
Stanford |
State/province |
California |
ZIP/Postal code |
94305-5101 |
Country |
USA |
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Platforms (1) |
GPL13112 |
Illumina HiSeq 2000 (Mus musculus) |
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Samples (6)
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Relations |
BioProject |
PRJNA278162 |
SRA |
SRP056154 |