Lu J, Guo S, Ebert BL, Zhang H, Peng X, Bosco J, Pretz J, Schlanger R, Wang JY, Mak RH, et al. MicroRNA-mediated control of cell fate in megakaryocyte-erythrocyte progenitors. Dev Cell. 2008;14:843–53.
NOTES
Lu, JunGuo, ShangqinEbert, Benjamin LZhang, HaoPeng, XiaoBosco, JocelynPretz, JenniferSchlanger, RitaWang, Judy YMak, Raymond HDombkowski, David MPreffer, Frederic IScadden, David TGolub, Todd RengHoward Hughes Medical Institute/Research Support, Non-U.S. Gov'tDev Cell. 2008 Jun;14(6):843-53. doi: 10.1016/j.devcel.2008.03.012.
Abstract
Lineage specification is a critical issue in developmental and regenerative biology. We hypothesized that microRNAs (miRNAs) are important participants in those processes and used the poorly understood regulation of megakaryocyte-erythrocyte progenitors (MEPs) in hematopoiesis as a model system. We report here that miR-150 modulates lineage fate in MEPs. Using a novel methodology capable of profiling miRNA expression in small numbers of primary cells, we identify miR-150 as preferentially expressed in the megakaryocytic lineage. Through gain- and loss-of-function experiments, we demonstrate that miR-150 drives MEP differentiation toward megakaryocytes at the expense of erythroid cells in vitro and in vivo. Moreover, we identify the transcription factor MYB as a critical target of miR-150 in this regulation. These experiments show that miR-150 regulates MEP fate, and thus establish a role for miRNAs in lineage specification of mammalian multipotent cells.
Last updated on 02/17/2021