JMD Conference & Exhibition
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental Material
Right arrow Purchase Article
Right arrow View Shopping Cart
Services
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Margraf, R. L.
Right arrow Articles by Wittwer, C. T.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Margraf, R. L.
Right arrow Articles by Wittwer, C. T.
JMD 2007, Vol. 9, No. 2
Copyright © 2007 American Society for Investigative Pathology & Association for Molecular Pathology

RET Proto-Oncogene Genotyping Using Unlabeled Probes, the Masking Technique, and Amplicon High-Resolution Melting Analysis

Rebecca L. Margraf*, Rong Mao*{dagger}, W. Edward Highsmith{ddagger}, Leonard M. Holtegaard{ddagger} and Carl T. Wittwer*{dagger}

From the ARUP Institute for Clinical and Experimental Pathology, * Salt Lake City, Utah; the Department of Pathology, {dagger} University of Utah Medical School, Salt Lake City, Utah; and the Molecular Genetics Laboratory, {ddagger} Mayo Clinic, Rochester, Minnesota

Single bp mutations in the RET proto-oncogene can cause multiple endocrine neoplasia type 2 syndromes. The conventional approach for genotyping RET mutations is sequencing the exons. A closed-tube RET genotyping assay using a saturating DNA dye, unlabeled probes, and amplicon high-resolution melting analysis was developed. The method required two sequential polymerase chain reaction stages, a primary and secondary assay. The primary assay analyzed RET exons 10, 11, 13, 14, and 16 with a total of seven reactions using eight unlabeled probes. The primary assay genotyped wild-type exons, a common exon 13 polymorphism, and an exon 16 mutation, whereas other RET sequence variation was detected. The primary unlabeled probe data limited the possible genotypes for the detected RET sequence variation, which permitted genotyping in a secondary assay with only two to five reactions. Six probes were designed with the masking technique and masked selected sequence variations to allow unambiguous analysis of other mutations elsewhere under the probe. After this two-stage RET genotyping assay, less than 0.2% of exons tested would require sequencing for genotype. A blinded study generated from five wild type and 29 available RET sequence variation samples was 100% concordant with sequencing. Amplicon high-resolution melting analysis with unlabeled probes and the masking technique is a fast, accurate method for genotyping the >50 RET sequence variations.




This article has been cited by other articles:


Home page
J. Mol. Diagn.Home page
R. L. Margraf, R. Mao, and C. T. Wittwer
Rapid Diagnosis of MEN2B Using Unlabeled Probe Melting Analysis and the LightCycler 480 Instrument
J. Mol. Diagn., March 1, 2008; 10(2): 123 - 128.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
M. T. Seipp, D. Pattison, J. D. Durtschi, M. Jama, K. V. Voelkerding, and C. T. Wittwer
Quadruplex Genotyping of F5, F2, and MTHFR Variants in a Single Closed Tube by High-Resolution Amplicon Melting
Clin. Chem., January 1, 2008; 54(1): 108 - 115.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
J. Montgomery, C. T. Wittwer, J. O. Kent, and L. Zhou
Scanning the Cystic Fibrosis Transmembrane Conductance Regulator Gene Using High-Resolution DNA Melting Analysis
Clin. Chem., November 1, 2007; 53(11): 1891 - 1898.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
S. Dames, D. C. Pattison, L. K. Bromley, C. T. Wittwer, and K. V. Voelkerding
Unlabeled Probes for the Detection and Typing of Herpes Simplex Virus
Clin. Chem., October 1, 2007; 53(10): 1847 - 1854.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 by the American Society for Investigative Pathology and the Association for Molecular Pathology.