Validation of a commercially available test that enables the quantification of the numbers of CGG trinucleotide repeat expansion in FMR1 gene

被引:10
|
作者
Lim, Grace X. Y. [1 ]
Yeo, Minli [1 ]
Koh, Yvonne Y. [1 ]
Winarni, Tri Indah [2 ]
Rajan-Babu, Indhu-Shree [3 ]
Chong, Samuel S. [3 ,4 ,5 ]
Faradz, Sultana M. H. [2 ]
Guan, Ming [1 ]
机构
[1] BioFactory Pte Ltd, Singapore, Singapore
[2] Diponegoro Univ, Div Human Genet, Ctr Biomed Res, Fac Med, Semarang, Indonesia
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Paediat, Singapore, Singapore
[4] Natl Univ Hlth Syst, Khoo Teck Puat Natl Univ Childrens Med Inst, Singapore, Singapore
[5] Natl Univ Singapore Hosp, Dept Lab Med, Singapore, Singapore
来源
PLOS ONE | 2017年 / 12卷 / 03期
关键词
FRAGILE-X-SYNDROME; EXPANDED ALLELES; PRIMED PCR; FULL MUTATIONS; GUIDELINES; IDENTIFICATION; DISORDERS; DIAGNOSIS; NEWBORN; ASSAY;
D O I
10.1371/journal.pone.0173279
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the present study, we evaluated a commercially available TP-PCR-based assay, the FastFraX(TM) FMR1 Sizing kit, as a test in quantifying the number of CGG repeats in the FMR1 gene. Based on testing with well characterized DNA samples from Coriell, the kit yielded size results within 3 repeats of those obtained by common consensus (n = 14), with the exception of one allele. Furthermore, based on data obtained using all Coriell samples with or without common consensus (n = 29), the Sizing kit was 97.5% in agreement with existing approaches. Additionally, the kit generated consistent size information in repeatability and reproducibility studies (CV 0.39% to 3.42%). Clinical performance was established with 198 archived clinical samples, yielding results of 100% sensitivity (95% CI, 91.03% to 100%) and 100% specificity (95% CI, 97.64% to 100%) in categorizing patient samples into the respective normal, intermediate, premutation and full mutation genotypes.
引用
收藏
页数:15
相关论文
共 33 条
  • [1] Validation of a Commercially Available Screening Tool for the Rapid Identification of CGG Trinucleotide Repeat Expansions in FMR1
    Lim, Grace X. Y.
    Loo, Yu Ling
    Mundhofir, Farmaditya E. P.
    Cayami, Ferdy K.
    Faradz, Sultana M. H.
    Rajan-Babu, Indhu-Shree
    Chong, Samuel S.
    Koh, Yvonne Y.
    Guan, Ming
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2015, 17 (03) : 302 - 314
  • [2] Validation of a Screening Tool for the Rapid and Reliable Detection of CGG Trinucleotide Repeat Expansions in FMR1
    Basehore, Monica J.
    Marlowe, Natalia M.
    Jones, Julie R.
    Behlendorf, Deborah E.
    Laver, Thomas A.
    Friez, Michael J.
    GENETIC TESTING AND MOLECULAR BIOMARKERS, 2012, 16 (06) : 465 - 470
  • [3] CGG repeat in the FMR1 gene: size matters
    Willemsen, R.
    Levenga, J.
    Oostra, B. A.
    CLINICAL GENETICS, 2011, 80 (03) : 214 - 225
  • [4] The prevalence of CGG repeat expansion mutation in FMR1 gene in the northern Chinese women of reproductive age
    Ma, Yinan
    Wei, Xing
    Pan, Hong
    Wang, Songtao
    Wang, Xin
    Liu, Xiaowei
    Zou, Liying
    Wang, Xiaomei
    Wang, Xiaorong
    Yang, Hua
    Wang, Fengying
    Wang, Kefang
    Sun, Lifang
    Qiao, Xiaolin
    Yang, Yue
    Ma, Xiuhua
    Liu, Dandan
    Ding, Guifeng
    Ma, Junqi
    Yang, Xiuli
    Zhu, Sainan
    Qi, Yu
    Yin, Chenghong
    BMC MEDICAL GENETICS, 2019, 20
  • [5] Distribution and frequency of FMR1 CGG repeat numbers in the general population
    Holden, JJA
    Chalifoux, M
    Wing, M
    JulienInalsingh, C
    Lawson, JS
    Higgins, JV
    Sherman, S
    White, BN
    DEVELOPMENTAL BRAIN DYSFUNCTION, 1995, 8 (4-6): : 405 - 407
  • [6] PGT-M for Premature Ovarian Failure Related to CGG Repeat Expansion of the FMR1 Gene
    Persico, Tiziana
    Tranquillo, Maria Lucrezia
    Seracchioli, Renato
    Zuccarello, Daniela
    Sorrentino, Ugo
    GENES, 2024, 15 (01)
  • [7] Screening for FMR1 CGG Repeat Expansion in Thai Patients with Autism Spectrum Disorder
    Hnoonual, Areerat
    Jankittunpaiboon, Charunee
    Limprasert, Pornprot
    BIOMED RESEARCH INTERNATIONAL, 2021, 2021
  • [8] New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease
    Loesch, D. Z.
    Tassone, F.
    Lo, J.
    Slater, H. R.
    Hills, L. V.
    Bui, M. Q.
    Silburn, P. A.
    Mellick, G. D.
    CLINICAL GENETICS, 2013, 84 (04) : 382 - 385
  • [9] Chromatin changes caused by expansion of CGG repeats in fmr1 gene
    D. V. Yudkin
    N. A. Lemskaya
    I. V. Grischenko
    A. A. Dolskiy
    Molecular Biology, 2015, 49 : 179 - 184
  • [10] Chromatin changes caused by expansion of CGG repeats in fmr1 gene
    Yudkin, D. V.
    Lemskaya, N. A.
    Grischenko, I. V.
    Dolskiy, A. A.
    MOLECULAR BIOLOGY, 2015, 49 (02) : 179 - 184