Gfi1 regulates miR-21 and miR-196b to control myelopoiesis

Blood. 2009 May 7;113(19):4720-8. doi: 10.1182/blood-2008-11-190215. Epub 2009 Mar 10.

Abstract

The zinc finger protein growth factor independent-1 (Gfi1) is a transcriptional repressor that is critically required for normal granulocytic differentiation. GFI1 loss-of-function mutations are found in some patients with severe congenital neutropenia (SCN). The SCN-associated GFI1-mutant proteins act as dominant negatives to block granulopoiesis through selective deregulation of a subset of GFI1 target genes. Here we show that Gfi1 is a master regulator of microRNAs, and that deregulated expression of these microRNAs recapitulates a Gfi1 loss-of-function block to granulocyte colony-stimulating factor (G-CSF)-stimulated granulopoiesis. Specifically, bone marrow cells from a GFI1-mutant SCN patient and Gfi1(-/-) mice display deregulated expression of miR-21 and miR-196B expression. Flow cytometric analysis and colony assays reveal that the overexpression or depletion of either miR induces changes in myeloid development. However, coexpression of miR-21 and miR-196b (as seen in Gfi1(-/-) mice and a GFI1N382S SCN patient) completely blocks G-CSF-induced granulopoiesis. Thus, our results not only identify microRNAs whose regulation is required during myelopoiesis, but also provide an example of synergy in microRNA biologic activity and illustrate potential mechanisms underlying SCN disease pathogenesis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow / physiology*
  • Bone Marrow Transplantation
  • Chromatin Immunoprecipitation
  • Colony-Forming Units Assay
  • DNA-Binding Proteins / physiology*
  • Electrophoretic Mobility Shift Assay
  • Female
  • Flow Cytometry
  • Gene Expression Profiling
  • Granulocyte Colony-Stimulating Factor / pharmacology
  • Granulocytes / cytology
  • Granulocytes / physiology
  • Hematopoietic Stem Cells
  • Immunoblotting
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • MicroRNAs / genetics*
  • MicroRNAs / physiology
  • Myelopoiesis / physiology*
  • Oligonucleotide Array Sequence Analysis
  • RNA, Small Interfering / pharmacology
  • Transcription Factors / physiology*

Substances

  • DNA-Binding Proteins
  • Gfi1 protein, mouse
  • MIRN21 microRNA, mouse
  • MicroRNAs
  • RNA, Small Interfering
  • Transcription Factors
  • Granulocyte Colony-Stimulating Factor