MIR-23A microRNA cluster inhibits B-cell development

Kimi Y. Kong, Kristin S. Owens, Jason H. Rogers, Jason Mullenix, Chinavenmeni S. Velu, H. Leighton Grimes, Richard Dahl

Research output: Contribution to journalArticle

73 Citations (Scopus)

Abstract

Objective: The transcription factor PU.1 (encoded by Sfpi1) promotes myeloid differentiation, but it is unclear what downstream genes are involved. Micro RNAs (miRNAs) are a class of small RNAs that regulate many cellular pathways, including proliferation, survival, and differentiation. The objective of this study was to identify miRNAs downstream of PU.1 that regulate hematopoietic development. Materials and Methods: miRNAs that change expression in a PU.1-inducible cell line were identified with microarrays. The promoter for an miRNA cluster upregulated by PU.1 induction was analyzed for PU.1 binding by electrophoretic mobility shift and chromatin immunoprecipitation assays. Retroviral transduction of hematopoietic progenitors was performed to evaluate the effect of miRNA expression on hematopoietic development in vitro and in vivo. Results: We identified an miRNA cluster whose pri-transcript is regulated by PU.1. The pri-miRNA encodes three mature miRNAs: miR-23a, miR-27a, and miR-24-2. Each miRNA is more abundant in myeloid cells compared to lymphoid cells. When hematopoietic progenitors expressing the 23a cluster miRNAs were cultured in B-cell-promoting conditions, we observed a dramatic decrease in B lymphopoiesis and an increase in myelopoiesis compared to control cultures. In vivo, hematopoietic progenitors expressing the miR-23a cluster generate reduced numbers of B cells compared to control cells. Conclusions: The miR-23a cluster is a downstream target of PU.1 involved in antagonizing lymphoid cell fate acquisition. Although miRNAs have been identified downstream of PU.1 in mediating development of monocytes and granulocytes, the 23a cluster is the first downstream miRNA target implicated in regulating development of myeloid vs lymphoid cells.

Original languageEnglish (US)
JournalExperimental Hematology
Volume38
Issue number8
DOIs
StatePublished - Aug 2010
Externally publishedYes

Fingerprint

MicroRNAs
B-Lymphocytes
Lymphocytes
Lymphopoiesis
Myelopoiesis
Chromatin Immunoprecipitation
Myeloid Cells
Granulocytes
Monocytes
RNA
Cell Line

ASJC Scopus subject areas

  • Cancer Research
  • Cell Biology
  • Genetics
  • Molecular Biology
  • Hematology

Cite this

Kong, K. Y., Owens, K. S., Rogers, J. H., Mullenix, J., Velu, C. S., Grimes, H. L., & Dahl, R. (2010). MIR-23A microRNA cluster inhibits B-cell development. Experimental Hematology, 38(8). https://doi.org/10.1016/j.exphem.2010.04.004

MIR-23A microRNA cluster inhibits B-cell development. / Kong, Kimi Y.; Owens, Kristin S.; Rogers, Jason H.; Mullenix, Jason; Velu, Chinavenmeni S.; Grimes, H. Leighton; Dahl, Richard.

In: Experimental Hematology, Vol. 38, No. 8, 08.2010.

Research output: Contribution to journalArticle

Kong, KY, Owens, KS, Rogers, JH, Mullenix, J, Velu, CS, Grimes, HL & Dahl, R 2010, 'MIR-23A microRNA cluster inhibits B-cell development', Experimental Hematology, vol. 38, no. 8. https://doi.org/10.1016/j.exphem.2010.04.004
Kong KY, Owens KS, Rogers JH, Mullenix J, Velu CS, Grimes HL et al. MIR-23A microRNA cluster inhibits B-cell development. Experimental Hematology. 2010 Aug;38(8). https://doi.org/10.1016/j.exphem.2010.04.004
Kong, Kimi Y. ; Owens, Kristin S. ; Rogers, Jason H. ; Mullenix, Jason ; Velu, Chinavenmeni S. ; Grimes, H. Leighton ; Dahl, Richard. / MIR-23A microRNA cluster inhibits B-cell development. In: Experimental Hematology. 2010 ; Vol. 38, No. 8.
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