Disruption of Myc-tubulin interaction by hyperphosphorylation of c-Myc during mitosis or by constitutive hyperphosphorylation of mutant c-Myc in Burkitt's lymphoma

Mol Cell Biol. 2000 Jul;20(14):5276-84. doi: 10.1128/MCB.20.14.5276-5284.2000.

Abstract

Somatic mutations at Thr-58 of c-Myc have been detected in Burkitt's lymphoma (BL) tumors and have been shown to affect the transforming potential of the Myc oncoprotein. In addition, the N-terminal domain of c-Myc has been shown to interact with microtubules in vivo, and the binding of c-Myc to alpha-tubulin was localized to amino acids 48 to 135 within the c-Myc protein. We demonstrate that c-Myc proteins harboring a naturally occurring mutation at Thr-58 from BL cell lines have increased stability and are constitutively hyperphosphorylated, which disrupts the in vivo interaction of c-Myc with alpha-tubulin. In addition, we show that wild-type c-Myc-alpha-tubulin interactions are also disrupted during a transient mitosis-specific hyperphosphorylation of c-Myc, which resembles the constitutive hyperphosphorylation pattern of Thr-58 in BL cells.

MeSH terms

  • Amino Acid Substitution
  • Burkitt Lymphoma / genetics*
  • Burkitt Lymphoma / pathology
  • Cell Line
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Microtubules / metabolism
  • Mitosis*
  • Mutation
  • Peptide Mapping
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Proto-Oncogene Proteins c-myc / genetics*
  • Proto-Oncogene Proteins c-myc / metabolism*
  • Tubulin / metabolism*

Substances

  • Phosphoproteins
  • Proto-Oncogene Proteins c-myc
  • Tubulin