Abstract | BACKGROUND: METHODS: We sought to develop a pre-screening method in the diagnostic procedure and pursued variant scanning by high-resolution melting analysis (HRM) on a LightScanner instrument. We used 50 samples, representing 45 different rare variants, to validate the HRM method. In addition, we implemented small amplicon genotyping of three frequent CASR variants (c.1732+16T/C, c.2956G>T and c.2968A>G). RESULTS: Using HRM, we identified 43 of 45 variants confidently (~96%) while two variants escaped immediate detection. Implementing this method in clinical use further resulted in the identification of seven new CASR variants and nine recurrent. HRM variant scanning, in combination with small amplicon genotyping, provides a simple workflow with reduced sequencing burden. Bioinformatics analyses using two freely available prediction tools (PolyPhen2 and SIFT) for evaluating amino acid substitutions were compared and indicated discrepancies in the prediction for 25% of the variants. CONCLUSION: This study demonstrates the utility of HRM as a pre-screening method, adds 24 novel rare CASR variants, and further emphasizes the importance of clinical decision making based on all available information rather than bioinformatics alone.
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Authors | Peter H Nissen, Signe E Christensen, Søren A Ladefoged, Kim Brixen, Lene Heickendorff, Leif Mosekilde |
Journal | Clinica chimica acta; international journal of clinical chemistry
(Clin Chim Acta)
Vol. 413
Issue 5-6
Pg. 605-11
(Mar 22 2012)
ISSN: 1873-3492 [Electronic] Netherlands |
PMID | 22192860
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2011 Elsevier B.V. All rights reserved. |
Chemical References |
- CASR protein, human
- Receptors, Calcium-Sensing
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Topics |
- Computational Biology
- Genetic Testing
- Genetic Variation
(genetics)
- Humans
- Receptors, Calcium-Sensing
(genetics)
- Transition Temperature
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