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Ultra-sensitive Detection Of BRAF V600E And G469A Mutations By Ice COLD-PCR And BLOCker- Sequencing | 3649
ISSN-2155-9929

Journal of Molecular Biomarkers & Diagnosis
Open Access

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Ultra-sensitive detection of BRAF V600E and G469A mutations by Ice COLD-PCR and BLOCker- Sequencing

2nd World Congress on Biomarkers & Clinical Research

Yanggu Shi, Benjamin Legendre, Jr., Tyler Borcyk, Phil Eastlake and Katherine Richardson

ScientificTracks Abstracts: J Mol Biomark Diagn

DOI: 10.4172/2155-9929.S1.2

Abstract
BRAF, a serine/threonine kinase, mediates the RAS/RAF/MAPK signal transduction pathway. Over 90% of BRAF mutations are V600E (c.1796T>A); this activates mitogenic cascades leading to tumorigenesis. Th is mutation is present in 70% melanoma, 100% hairy cell leukemia, 40% papillary thyroid cancer and, less frequently, other cancer types. V600E mutation status is valuable for determining clinical diagnosis, companion diagnostic tests, treatment guidance and outcome prediction. Ice COLD-PCR (Improved & Complete Enrichment CO-amplifi cation at Lower Denaturation temperature) is technology that enriches mutated DNA sequences in an excess of wild-type DNA through selective amplifi cation of the mutant DNA population using LNA-modifi ed oligonucleotides (RS-oligo) complementary to wild-type sequence. Aft er Ice COLD-PCR enrichment, V600E mutations could be detected at 0.05% as confi rmed by standard Sanger sequencing. For the BRAF mutation G469A (c.1406G>C), limit of detection was 0.01%. We combined Ice COLD-PCR enrichment and dye terminator sequencing using a novel sequencing methodology, BLOCker-Sequencing (BLocking Oligonucleotide Cycle Sequencing). Wild-type strand sequencing is blocked by a BLOCker-oligo but mutant DNA is concurrently sequenced with one primer and amplifi ed with a 5? phosphate primer . Lambda exonuclease selectively removed all products resulting from incorporation of the primer containing the 5? phosphate. BLOCker-Sequencing aft er standard PCR increased the limit of V600E detection from 20% for standard Sanger sequencing to 1%. Th is compares favorably with other commercially available non-sequencing based mutation detection systems. Th e results presented here will demonstrate enhanced limits of detection when BLOCKer-Sequencing is used following Ice COLD-PCR amplifi cation.
Biography
Dr. Yanggu Shi completed his Ph.D. from New York University and postdoctoral studies from Columbia University College of Physicians and Surgeons. He is a Sr. Scientist at Transgenomic, Inc. Prior to this he was a Sr. Scientist at Human Genome Sciences, Inc.
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