Identification of G protein alpha subunit mutations in human growth hormone (GH)- and GH/prolactin-secreting pituitary tumors by single-strand conformation polymorphism (SSCP) analysis

Mol Cell Endocrinol. 1992 Sep;87(1-3):125-9. doi: 10.1016/0303-7207(92)90240-7.

Abstract

We have applied the polymerase chain reaction (PCR) and single-strand conformation polymorphism analysis (SSCP) to detect activating mutations in the Gs alpha subunit gene, amplifying genomic DNA extracted from growth hormone (GH)- and GH/prolactin (PRL)-secreting human pituitary tumors. Of 15 tumors tested six contained mutations in the analyzed regions of the Gs alpha. SSCP analysis revealed band shift in exon 8 in four GH- and in one GH/PRL-secreting tumors, and in exon 9 in one GH/PRL-secreting tumor. Direct sequencing of PCR reaction products identified the mutations as R201-H, R201-S and R201-C in exon 8 and Q227-L in exon 9. These results show the efficacy of PCR/SSCP analysis in the detection of G protein mutations and extend the generalization that these sites are hot spots in tumor-inducing mutations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoma / genetics*
  • Adenoma / metabolism
  • Base Sequence
  • Codon
  • DNA Mutational Analysis*
  • DNA, Neoplasm / genetics*
  • DNA, Single-Stranded / genetics*
  • Enzyme Activation
  • Exons
  • GTP Phosphohydrolases / genetics*
  • GTP-Binding Proteins / genetics*
  • Growth Hormone / metabolism*
  • Humans
  • Molecular Sequence Data
  • Mutation
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / metabolism
  • Nucleic Acid Conformation
  • Pituitary Neoplasms / genetics*
  • Pituitary Neoplasms / metabolism
  • Polymerase Chain Reaction
  • Prolactin / metabolism*

Substances

  • Codon
  • DNA, Neoplasm
  • DNA, Single-Stranded
  • Neoplasm Proteins
  • Prolactin
  • Growth Hormone
  • GTP Phosphohydrolases
  • GTP-Binding Proteins