Differential localization of hamartin and tuberin and increased S6 phosphorylation in a tuber

Neurology. 2004 Oct 12;63(7):1293-5. doi: 10.1212/01.wnl.0000140702.08902.d7.

Abstract

In a tuberous sclerosis patient with a mutation in the TSC1 tumor suppressor gene, no second-hit mutation was found in a resected cortical tuber. Tuber giant cells showed predominantly nuclear hamartin, cytosolic tuberin, and hyperphosphorylation of S6. Differential accumulation of hamartin and tuberin in separate cellular compartments of giant cells may prevent formation of the hamartin-tuberin complex, resulting in increased S6 phosphorylation. These data provide an alternative mechanism for tuberogenesis.

Publication types

  • Case Reports
  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cerebral Cortex / metabolism
  • Child
  • Epilepsy / etiology
  • Epilepsy / metabolism
  • Female
  • Germ-Line Mutation
  • Humans
  • Immunoenzyme Techniques
  • Nerve Tissue Proteins / metabolism*
  • Phosphorylation
  • Point Mutation
  • Repressor Proteins / metabolism*
  • Ribosomal Protein S6 / metabolism*
  • Tuberous Sclerosis / complications
  • Tuberous Sclerosis / genetics
  • Tuberous Sclerosis / metabolism*
  • Tuberous Sclerosis Complex 1 Protein
  • Tuberous Sclerosis Complex 2 Protein
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / metabolism*

Substances

  • Nerve Tissue Proteins
  • Repressor Proteins
  • Ribosomal Protein S6
  • TSC1 protein, human
  • TSC2 protein, human
  • Tuberous Sclerosis Complex 1 Protein
  • Tuberous Sclerosis Complex 2 Protein
  • Tumor Suppressor Proteins