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MicroRNA-Mediated Control of Cell Fate in Megakaryocyte-Erythrocyte Progenitors

  • Jun Lu
  • , 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

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish (US)
Pages (from-to)843-853
Number of pages11
JournalDevelopmental Cell
Volume14
Issue number6
DOIs
StatePublished - Jun 10 2008
Externally publishedYes

Keywords

  • DEVBIO
  • RNA

ASJC Scopus subject areas

  • Molecular Biology
  • General Biochemistry, Genetics and Molecular Biology
  • Developmental Biology
  • Cell Biology

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