A biochemical analysis demonstrates that the BRCA1 intronic variant IVS10-2A → C is a mutation Journal Article


Authors: Keaton, J. C.; Nielsen, D. R.; Hendrickson, B. C.; Pyne, M. T.; Scheuer, L.; Ward, B. E.; Brothman, A. R.; Scholl, T.
Article Title: A biochemical analysis demonstrates that the BRCA1 intronic variant IVS10-2A → C is a mutation
Abstract: Sequence analysis of cDNA from an asymptomatic patient belonging to a high-risk breast cancer family carrying the genetic variant BRCA1 IVS10-2A → C revealed that functional BRCA1 mRNA was derived from only one of the patient's chromosomes. The other chromosome produced an aberrant RNA splicing transcript that deleted exon 11. Analysis of the patient's genomic DNA demonstrated that the chromosome producing the non-functional mRNA carried the genotype BRCA1 IVS10-2A → C. This transversion disrupts a highly conserved base in the consensus splice acceptor motif. These results support the conclusion that BRCA1 IVS10-2A → C is a mutation that confers predisposition to breast and ovarian cancer.
Keywords: adult; gene mutation; sequence analysis; exon; gene deletion; mutation; case report; cancer risk; chemical analysis; cancer susceptibility; genetic predisposition to disease; ovary cancer; breast cancer; genetic variability; intron; introns; pedigree; oncogene; messenger rna; genes, brca1; nucleotide sequence; high risk population; sequence analysis, rna; point mutation; brca1; genomic dna; rna splicing; complementary dna; mrna; sequence analysis, dna; rna splice sites; splice; humans; human; male; female; article
Journal Title: Journal of Human Genetics
Volume: 48
Issue: 8
ISSN: 1434-5161
Publisher: Nature Publishing Group  
Date Published: 2003-08-01
Start Page: 399
End Page: 403
Language: English
DOI: 10.1007/s10038-003-0044-0
PUBMED: 14513821
PROVIDER: scopus
DOI/URL:
Notes: Export Date: 12 September 2014 -- Source: Scopus
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  1. Lauren   Scheuer
    18 Scheuer