A single nucleotide primer extension assay to detect the APC I1307K gene variant

Kathleen M. Murphy, Tanya Geiger, Michael J. Hafez, James R. Eshleman, Constance A. Griffin, Karin D. Berg

Research output: Contribution to journalArticle

Abstract

Adenomatous polyposis coli (APC) is a tumor suppressor gene important in colorectal tumorigenesis. A genetic variant of APC, I1307K, results from a T-to-A transversion at nucleotide 3920 which converts the wild-type sequence to a homopolymer tract (A8). The I1307K alteration is not itself oncogenic, but creates a hypermutable region (A8) that is prone to frame-shift mutations. The APC I1307K variant occurs in approximately 6% of the Ashkenazi Jewish population and is reported to approximately double an individual's risk for colorectal cancer. Here we describe a single nucleotide primer extension assay for the detection of the APC I1307K mutation. Following PCR amplification, nucleotide 3920 of the APC gene is directly sequenced using single nucleotide primer extension technology. The assay is in a multiplex format allowing simultaneous forward and reverse sequencing of the I1307K variant, which provides an internal, independent confirmation of each testing result. The assay was validated against 60 samples previously characterized by an allele-specific oligonucleotide (ASO) hybridization assay, with 100% concordance of results. Compared to the ASO assay, this single nucleotide primer extension assay requires significantly less technical time to perform, and has a greatly increased throughput capacity. The single nucleotide extension assay provides a highly sensitive and specific assay to identify individuals with the APC I1307K gene variant who may benefit from increased colorectal screening.

Original languageEnglish (US)
Pages (from-to)222-226
Number of pages5
JournalJournal of Molecular Diagnostics
Volume5
Issue number4
DOIs
StatePublished - Nov 2003

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Molecular Medicine

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