Nucleolar release of Hand1 acts as a molecular switch to determine cell fate

Nat Cell Biol. 2007 Oct;9(10):1131-41. doi: 10.1038/ncb1633. Epub 2007 Sep 23.

Abstract

The bHLH transcription factor Hand1 is essential for placentation and cardiac morphogenesis in the developing embryo. Here we implicate Hand1 as a molecular switch that determines whether a trophoblast stem cell continues to proliferate or commits to differentiation. We identify a novel interaction of Hand1 with a protein that contains an I-mfa (inhibitor of myogenic factor) domain that anchors Hand1 in the nucleolus where it negatively regulates Hand1 activity. In the trophoblast stem-cell line Rcho-1, nucleolar sequestration of Hand1 accompanies sustained cell proliferation and renewal, whereas release of Hand1 into the nucleus leads to its activation, thus committing cells to a differentiated giant-cell fate. Site-specific phosphorylation is required for nucleolar release of Hand1, for its dimerization and biological function, and this is mediated by the non-canonical polo-like kinase Plk4 (Sak). Sak is co-expressed in Rcho-1 cells, localizes to the nucleolus during G2 and phosphorylates Hand1 as a requirement for trophoblast stem-cell commitment to a giant-cell fate. This study defines a novel cellular mechanism for regulating Hand1 that is a crucial step in the stem-cell differentiation pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • Basic Helix-Loop-Helix Transcription Factors / physiology
  • Blotting, Northern
  • Blotting, Western
  • Cell Differentiation*
  • Cell Nucleolus / metabolism*
  • Cell Proliferation
  • Gene Expression Regulation, Developmental
  • Giant Cells / cytology
  • Giant Cells / metabolism
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Immunoprecipitation
  • Mice
  • Myogenic Regulatory Factors / metabolism
  • NIH 3T3 Cells
  • Phosphorylation
  • Protein Binding
  • Protein Phosphatase 2
  • Protein Serine-Threonine Kinases / metabolism
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stem Cells / cytology
  • Stem Cells / metabolism*
  • Trophoblasts / cytology
  • Trophoblasts / metabolism
  • Two-Hybrid System Techniques

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Hand1 protein, mouse
  • Mdfi protein, mouse
  • Myogenic Regulatory Factors
  • Recombinant Fusion Proteins
  • Green Fluorescent Proteins
  • Plk4 protein, mouse
  • Protein Serine-Threonine Kinases
  • Ppp2r5d protein, mouse
  • Protein Phosphatase 2