Regulation of B-cell development and tolerance by different members of the miR-17∼1/492 family microRNAs
Entity
UAM. Departamento de BioquímicaPublisher
Nature Research (part of Springer Nature)Date
2016-08-02Citation
10.1038/ncomms12207
Nature Communications 7.1 (2016): 2658
ISSN
2041-1723DOI
10.1038/ncomms12207Funded by
This study is supported by the PEW Charitable Trusts, Cancer Research Institute, Lupus Research Institute and National Institute of Health (R01AI087634, R01AI089854, R56AI110403 and R56AI121155 to C.X.)Editor's Version
https://doi.org/10.1038/ncomms12207Subjects
B-cell; Development and tolerance; miR-17B92; microRNAs; MedicinaRights
© The Author(s) 2016Abstract
The molecular mechanisms that regulate B-cell development and tolerance remain incompletely understood. In this study, we identify a critical role for the miR-17∼1/492 microRNA cluster in regulating B-cell central tolerance and demonstrate that these miRNAs control early B-cell development in a cell-intrinsic manner. While the cluster member miR-19 suppresses the expression of Pten and plays a key role in regulating B-cell tolerance, miR-17 controls early B-cell development through other molecular pathways. These findings demonstrate differential control of two closely linked B-cell developmental stages by different members of a single microRNA cluster through distinct molecular pathways
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Google Scholar:Lai, Maoyi
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Gonzalez-Martin, Alicia
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Cooper, Anthony B.
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Oda, Hiroyo
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Jin, Hyun Yong
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Shepherd, Jovan
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He, Linling
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Zhu, Jiang
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Nemazee, David
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Xiao, Changchun
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