An acceptor splice site mutation in the calcium-sensing receptor (CASR) gene in familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Hum Mutat. 2001 Nov;18(5):411-21. doi: 10.1002/humu.1212.

Abstract

We studied family members of a large kindred expressing both familial hypocalciuric hypercalcemia (FHH) and neonatal severe hyperparathyroidism (NSHPT) and found, by PCR amplification of the extracellular calcium-sensing receptor (CASR) gene exons and flanking intronic sequences, that FHH individuals were heterozygous for a g to t substitution in the last nucleotide of intron 2 (IVS2-1G>T). Defects in messenger RNA splicing were investigated by illegitimate transcription of the CASR gene in lymphoblastoid cells from an FHH affected individual, as well as by transfection of a CASR minigene harboring this mutation into HEK293 cells. The mutation resulted predominantly in exon III skipping causing a shift in exon IV reading frame and introduction of a premature stop codon leading to a predicted truncated protein of 153 amino acids. Interestingly, it was noted that exon III splicing is not 100% efficient in parathyroid, thyroid, and kidney; an exon III-deleted transcript is produced approximately 15% of the time. This is the first description of a splice site mutation in the CASR gene and provides an explanation of the clinical phenotype of the patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing / genetics*
  • Base Sequence
  • Cell Line
  • Codon, Nonsense / genetics
  • DNA Mutational Analysis
  • Exons / genetics
  • Female
  • Humans
  • Hypercalcemia / genetics*
  • Hyperparathyroidism / genetics*
  • Infant, Newborn
  • Introns / genetics
  • Male
  • Mutation / genetics*
  • Nuclease Protection Assays
  • Open Reading Frames / genetics
  • Pedigree
  • RNA Splice Sites / genetics*
  • RNA, Messenger / analysis
  • RNA, Messenger / genetics
  • Receptors, Calcium-Sensing
  • Receptors, Cell Surface / chemistry
  • Receptors, Cell Surface / genetics*
  • Receptors, Cell Surface / metabolism
  • Sequence Deletion / genetics
  • Transcription, Genetic / genetics
  • Transfection

Substances

  • Codon, Nonsense
  • RNA Splice Sites
  • RNA, Messenger
  • Receptors, Calcium-Sensing
  • Receptors, Cell Surface