Identification of two novel mouse nuclear proteins that bind selectively to a methylated c-Myc recognizing sequence

Nucleic Acids Res. 1993 May 11;21(9):2125-30. doi: 10.1093/nar/21.9.2125.

Abstract

The c-Myc recognizes the sequence CACGTG (Blackwell, T. K., Kretzner, L., Blackwood, E.M., Eisenman, R. N., and Weintraub, H. (1990) Science 250, 1149-1151), and its binding is inhibited by methylation of the core CpG (Prendergast, G. C. and Ziff, E. B. (1991) Science 251, 186-189). We identified two novel nuclear proteins, MMBP-1 and MMBP-2, that bound specifically and under physiological salt condition to the c-Myc binding motif of which cytidine in the CpG sequence was methylated. MMBP-1 was about 42 kD and MMBP-2 was about 63 kD. MMBP-1 was found in specific cells, while MMBP-2 was found in all the cell lines tested, suggesting that MMBP-1 may modulate the role of MMBP-2 in tissue specific manner. We propose that the two proteins play a role in the regulation of c-Myc function through stabilizing or destabilizing the methylation state of the c-Myc binding motif.

MeSH terms

  • Animals
  • Base Sequence
  • Binding Sites
  • Cell Fractionation
  • Cell Line
  • DNA / metabolism*
  • DNA-Binding Proteins / metabolism*
  • Male
  • Methylation
  • Mice
  • Molecular Sequence Data
  • Nuclear Proteins / metabolism*
  • Proto-Oncogene Proteins c-myc / metabolism*

Substances

  • DNA-Binding Proteins
  • Nuclear Proteins
  • Proto-Oncogene Proteins c-myc
  • DNA