Redefinition of the coding sequence of the MXI1 gene and identification of a polymorphic repeat in the 3' non-coding region that allows the detection of loss of heterozygosity of chromosome 10q25 in glioblastomas

Hum Genet. 1995 Jun;95(6):709-11. doi: 10.1007/BF00209493.

Abstract

The MXI1 gene encodes a protein interacting with Max, a regulatory factor of the Myc oncogene, and is located on chromosome 10q25, a region showing frequent loss of heterozygosity in malignant gliomas. We have reassessed the coding sequence of MXI1 and found that, at the 3' end, the open reading frame is 28 codons shorter than previously described. We have also found an AAAAC polymorphic repeat (two alleles, 45% heterozygosity) in the 3' non-coding region of the gene. Six anaplastic astrocytomas and nine glioblastomas, the most malignant form of glioma, were informative for this polymorphism. Loss of heterozygosity was demonstrated in all glioblastomas, but not in the remaining tumors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Basic Helix-Loop-Helix Transcription Factors
  • Brain Neoplasms / genetics*
  • Chromosomes, Human, Pair 10 / genetics*
  • DNA-Binding Proteins / genetics*
  • Genes, Tumor Suppressor / genetics
  • Glioblastoma / genetics*
  • Heterozygote
  • Humans
  • Molecular Sequence Data
  • Open Reading Frames / genetics*
  • Polymorphism, Genetic
  • Regulatory Sequences, Nucleic Acid / genetics
  • Repetitive Sequences, Nucleic Acid / genetics
  • Transcription Factors*
  • Tumor Suppressor Proteins

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • DNA-Binding Proteins
  • MXI1 protein, human
  • Transcription Factors
  • Tumor Suppressor Proteins

Associated data

  • GENBANK/S78470