Please use this identifier to cite or link to this item:
Title: A single common assay for robust and rapid fragile X mental retardation syndrome screening from dried blood spots
Authors: Tan, V.J.
Lian, M. 
Faradz, S.M.H.
Winarni, T.I..
Chong, S.S. 
Keywords: Dried blood spot
Fragile X syndrome
Melt curve analysis (MCA)
Trinucleotide repeat
Triplet-primed PCR (TP-PCR)
Issue Date: 2018
Publisher: Frontiers Media S.A.
Citation: Tan, V.J., Lian, M., Faradz, S.M.H., Winarni, T.I.., Chong, S.S. (2018). A single common assay for robust and rapid fragile X mental retardation syndrome screening from dried blood spots. Frontiers in Genetics 9 : 582. ScholarBank@NUS Repository.
Rights: Attribution 4.0 International
Abstract: Background: FMR1 CGG trinucleotide repeat hyper-expansions are observed in 99% of individuals with fragile X mental retardation syndrome (FXS). We evaluated the reliability of a rapid single-step gender-neutral molecular screen for FXS when performed on DNA isolated from dried blood spots. Methods: DNA was extracted from dried blood spots of 151 individuals with intellectual disability or autism spectrum disorder, whose FMR1 repeat genotypes are known. Dried blood spots were blinded prior to DNA extraction and analysis by triplet primed PCR (TP-PCR) and melt curve analysis (MCA). All expansion-positive and representative expansion-negative samples were also genotyped by fluorescent TP-PCR and capillary electrophoresis (CE) to confirm repeat expansion status. Results: Three males and 12 females were classified as expanded by TP-PCR MCA, and were subsequently sized by fluorescent TP-PCR CE. Two males and four females carried premutations, while one male and eight females carried full mutations. All 19 non-expanded samples that were sized were confirmed as carrying only normal alleles. Replicate analysis of representative expansion-positive samples yielded reproducible melt peak profiles. TP-PCR MCA classifications were completely concordant with FMR1 CGG repeat genotypes. Conclusion: TP-PCR MCA of dried blood spot DNA accurately and reliably identifies presence/absence of FMR1 CGG repeat expansions in both genders simultaneously. This strategy may be suitable for rapid high-throughput first-tier screening for fragile X syndrome. Copyright © 2018 Tan, Lian, Faradz, Winarni and Chong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).
Source Title: Frontiers in Genetics
ISSN: 16648021
DOI: 10.3389/fgene.2018.00582
Rights: Attribution 4.0 International
Appears in Collections:Elements
Staff Publications

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_3389_fgene_2018_00582.pdf4.64 MBAdobe PDF



Google ScholarTM



This item is licensed under a Creative Commons License Creative Commons