MiR-150 Controls B Cell Differentiation by Targeting the Transcription Factor c-Myb
Author(s) -
Changchun Xiao,
Dinis Pedro Calado,
Gunther R. Galler,
ToHa Thai,
Heide Christine Patterson,
Jing Wang,
Nikolaus Rajewsky,
Timothy P. Bender,
Klaus Rajewsky
Publication year - 2016
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2016.04.056
Subject(s) - biology , myb , transcription factor , progenitor cell , microrna , microbiology and biotechnology , cancer research , genetics , gene , stem cell
MiR-150 is a microRNA (miRNA) specifically expressed in mature lymphocytes, but not their progenitors. A top predicted target of miR-150 is c-Myb, a transcription factor controlling multiple steps of lymphocyte development. Combining loss- and gain-of-function gene targeting approaches for miR-150 with conditional and partial ablation of c-Myb, we show that miR-150 indeed controls c-Myb expression in vivo in a dose-dependent manner over a narrow range of miRNA and c-Myb concentrations and that this dramatically affects lymphocyte development and response. Our results identify a key transcription factor as a critical target of a stage-specifically expressed miRNA in lymphocytes and suggest that this and perhaps other miRNAs have evolved to control the expression of just a few critical target proteins in particular cellular contexts.
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