Myc binds the pluripotency factor Utf1 through the basic-helix-loop-helix leucine zipper domain

Biochem Biophys Res Commun. 2013 Jun 14;435(4):551-6. doi: 10.1016/j.bbrc.2013.04.100. Epub 2013 May 9.

Abstract

In order to elucidate the function of Myc in the maintenance of pluripotency and self-renewal in mouse embryonic stem cells (mESCs), we screened for novel ESC-specific interactors of Myc by mass spectrometry. Undifferentiated embryonic cell transcription factor 1 (Utf1) was identified in the screen as a putative Myc binding protein in mESCs. We found that Myc and Utf1 directly interact. Utf1 is a chromatin-associated factor required for maintaining pluripotency and self-renewal in mESCs. It can also replace c-myc during induced pluripotent stem cell (iPSC) generation with relatively high efficiency, and shares target genes with Myc in mESCs highlighting a potentially redundant functional role between Myc and Utf1. A large region of Utf1 was found to be necessary for direct interaction with N-Myc, while the basic helix-loop-helix leucine zipper domain of N-Myc is necessary for direct interaction with Utf1.

Publication types

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

MeSH terms

  • Animals
  • Binding Sites
  • Cell Line
  • Cells, Cultured
  • Chromosomal Proteins, Non-Histone
  • Leucine Zippers / physiology*
  • Mice
  • Pluripotent Stem Cells / metabolism*
  • Protein Binding
  • Protein Structure, Tertiary
  • Proto-Oncogene Proteins c-myc / chemistry*
  • Proto-Oncogene Proteins c-myc / metabolism*
  • Trans-Activators / chemistry*
  • Trans-Activators / metabolism*

Substances

  • Chromosomal Proteins, Non-Histone
  • Myc protein, mouse
  • Proto-Oncogene Proteins c-myc
  • Trans-Activators
  • Utf1 protein, mouse