A heterozygous 4-bp deletion mutation in the Gs alpha gene (GNAS1) in a patient with Albright hereditary osteodystrophy

Genomics. 1992 Aug;13(4):1319-21. doi: 10.1016/0888-7543(92)90056-x.

Abstract

Several heterozygous mutations within the gene encoding the alpha-subunit of Gs (GNAS1), the G protein that stimulates adenylyl cyclase, have been previously identified in patients with Albright hereditary osteodystrophy (AHO). We have now identified a fourth GNAS1 mutation from an AHO patient. Amplification by the polymerase chain reaction (PCR) of a genomic fragment encompassing GNAS1 exons 7 and 8 from one patient resulted in a product with aberrant migration on nondenaturing polyacrylamide and agarose gels. Direct DNA sequencing identified a 4-bp deletion in one allele of exon 7 encoding a frameshift with a premature stop codon. Analysis of lymphocyte RNA by reverse transcription-PCR and direct sequencing showed that the GNAS1 allele bearing the mutation is not expressed as mRNA. Consistent with this, Northern analysis revealed an approximate 50% deficiency in steady-state levels of GNAS1 mRNA. These findings further illustrate the heterogeneity of GNAS1 gene defects in AHO.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Blotting, Northern
  • Chromosome Deletion*
  • DNA
  • Electrophoresis, Agar Gel
  • Electrophoresis, Polyacrylamide Gel
  • Frameshift Mutation
  • GTP-Binding Proteins / genetics*
  • Heterozygote*
  • Humans
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Pseudohypoparathyroidism / genetics*
  • RNA, Messenger / metabolism
  • Transcription, Genetic

Substances

  • RNA, Messenger
  • DNA
  • GTP-Binding Proteins