Single-cell analysis reveals key roles for Bcl11a in regulating stem cell fate decisions

Genome Biol. 2015 Sep 21;16(1):199. doi: 10.1186/s13059-015-0778-y.

Abstract

Cell-cycle fluctuations drive significant transcriptomic heterogeneity in murine hematopoietic stem cells. Additionally, deletion of Bcl11a alters the regulation of hematopoietic stem cell quiescence, self-renewal, and fate choice.

MeSH terms

  • Animals
  • Carrier Proteins / genetics*
  • Cell Differentiation / genetics*
  • Cell Lineage / genetics
  • DNA-Binding Proteins
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / metabolism*
  • High-Throughput Nucleotide Sequencing
  • Mice
  • Nuclear Proteins / genetics*
  • Repressor Proteins
  • Signal Transduction
  • Single-Cell Analysis*
  • Thrombopoiesis / genetics

Substances

  • Bcl11a protein, mouse
  • Carrier Proteins
  • DNA-Binding Proteins
  • Nuclear Proteins
  • Repressor Proteins