| Literature DB >> 18539114 |
Jun Lu1, Shangqin Guo, Benjamin L Ebert, Hao Zhang, Xiao Peng, Jocelyn Bosco, Jennifer Pretz, Rita Schlanger, Judy Y Wang, Raymond H Mak, David M Dombkowski, Frederic I Preffer, David T Scadden, Todd R Golub.
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.Entities:
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Year: 2008 PMID: 18539114 PMCID: PMC2688789 DOI: 10.1016/j.devcel.2008.03.012
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270