14-3-3ζ interacts with hepatocyte nuclear factor 1α and enhances its DNA binding and transcriptional activation

Biochim Biophys Acta. 2013 Sep;1829(9):970-9. doi: 10.1016/j.bbagrm.2013.04.004. Epub 2013 Apr 16.

Abstract

14-3-3 proteins regulate numerous cellular processes through interaction with a variety of proteins, and have been identified as HNF1α binding partner by mass spectrometry analysis in our previous study. In the present study, the interaction between 14-3-3ζ and HNF1α has been further validated by in vivo and in vitro assays. Moreover, we have found that overexpression of 14-3-3ζ potentiated the transcriptional activity of HNF1α in cultured cells, and silencing of 14-3-3ζ by RNA interference in HepG2 cells specifically affected the HNF1α-dependent gene expression. Furthermore, we have demonstrated that 14-3-3ζ is recruited to endogenous HNF1α responsive promoters and enhances HNF1α binding to its cognate DNA sequences. In addition, we have also provided evidence that the association between HNF1α and 14-3-3ζ is phosphorylation-dependent. Taken together, these results suggest that 14-3-3ζ may be an endogenous physiologic regulator of HNF1α.

Keywords: 14-3-3; 14-3-3zeta; 14-3-3ζ; CIP; ChIP; EMSA; FRET; HNF; HNF1α; MODY; OA; Phosphorylation; Transcription regulation; calf intestinal alkaline phosphatase; chromatin-immunoprecipitation; electrophoretic mobility shift assay; fluorescence resonance energy transfer; hepatocyte nuclear factor; maturity onset diabetes of the young; okadaic acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 14-3-3 Proteins / metabolism*
  • Base Sequence
  • Cell Line, Tumor
  • DNA / metabolism*
  • DNA Primers
  • Hepatocyte Nuclear Factor 1-alpha / metabolism*
  • Humans
  • Phosphorylation
  • Protein Binding
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcriptional Activation*

Substances

  • 14-3-3 Proteins
  • DNA Primers
  • Hepatocyte Nuclear Factor 1-alpha
  • YWHAZ protein, human
  • DNA