Fast Temperature-Gradient COLD PCR for the enrichment of the paternally inherited SNPs in cell free fetal DNA; an application to non-invasive prenatal diagnosis of β-thalassaemia
To develop a sensitive, specific, simple, cost-effective and reproducible platform for the non-invasive prenatal detection of paternally inherited alleles for β-thalassaemia. The development of such an assay is of major significance in order to replace currently-applied invasive methods containing i...
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Published in: | PloS one Vol. 13; no. 7; p. e0200348 |
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Abstract | To develop a sensitive, specific, simple, cost-effective and reproducible platform for the non-invasive prenatal detection of paternally inherited alleles for β-thalassaemia. The development of such an assay is of major significance in order to replace currently-applied invasive methods containing inherent fetal loss risks.
We present a fast Temperature-Gradient Co-amplification at Lower Denaturation Temperature Polymerase Chain Reaction (fast TG COLD PCR) methodology for the detection of the paternally-inherited fetal alleles in maternal plasma. Two single-nucleotide polymorphisms (SNPs), rs7480526 (G/T) and rs968857 (G/A) that are located on the β-globin gene cluster and exhibit a high degree of heterozygosity in the Cypriot population were selected for evaluation. Seventeen maternal plasma samples from pregnancies at risk for β-thalassemia were analysed for the selected SNPs using the novel fast TG COLD PCR assay.
Using fast TG COLD PCR, the paternally inherited allele in cell free fetal DNA was correctly determined for all the 17 maternal plasma samples tested, showing full agreement with the Chorionic Villus Sampling (CVS) analysis.
Our findings are encouraging and demonstrate the efficiency and sensitivity of fast TG COLD PCR in detecting the minor paternally-inherited fetal alleles in maternal plasma for the development of a NIPD assay for β-thalassaemia. |
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AbstractList | Objective To develop a sensitive, specific, simple, cost-effective and reproducible platform for the non-invasive prenatal detection of paternally inherited alleles for β-thalassaemia. The development of such an assay is of major significance in order to replace currently-applied invasive methods containing inherent fetal loss risks. Methods We present a fast Temperature-Gradient Co-amplification at Lower Denaturation Temperature Polymerase Chain Reaction (fast TG COLD PCR) methodology for the detection of the paternally-inherited fetal alleles in maternal plasma. Two single-nucleotide polymorphisms (SNPs), rs7480526 (G/T) and rs968857 (G/A) that are located on the β-globin gene cluster and exhibit a high degree of heterozygosity in the Cypriot population were selected for evaluation. Seventeen maternal plasma samples from pregnancies at risk for β-thalassemia were analysed for the selected SNPs using the novel fast TG COLD PCR assay. Results Using fast TG COLD PCR, the paternally inherited allele in cell free fetal DNA was correctly determined for all the 17 maternal plasma samples tested, showing full agreement with the Chorionic Villus Sampling (CVS) analysis. Conclusions Our findings are encouraging and demonstrate the efficiency and sensitivity of fast TG COLD PCR in detecting the minor paternally-inherited fetal alleles in maternal plasma for the development of a NIPD assay for β-thalassaemia. To develop a sensitive, specific, simple, cost-effective and reproducible platform for the non-invasive prenatal detection of paternally inherited alleles for β-thalassaemia. The development of such an assay is of major significance in order to replace currently-applied invasive methods containing inherent fetal loss risks. We present a fast Temperature-Gradient Co-amplification at Lower Denaturation Temperature Polymerase Chain Reaction (fast TG COLD PCR) methodology for the detection of the paternally-inherited fetal alleles in maternal plasma. Two single-nucleotide polymorphisms (SNPs), rs7480526 (G/T) and rs968857 (G/A) that are located on the β-globin gene cluster and exhibit a high degree of heterozygosity in the Cypriot population were selected for evaluation. Seventeen maternal plasma samples from pregnancies at risk for β-thalassemia were analysed for the selected SNPs using the novel fast TG COLD PCR assay. Using fast TG COLD PCR, the paternally inherited allele in cell free fetal DNA was correctly determined for all the 17 maternal plasma samples tested, showing full agreement with the Chorionic Villus Sampling (CVS) analysis. Our findings are encouraging and demonstrate the efficiency and sensitivity of fast TG COLD PCR in detecting the minor paternally-inherited fetal alleles in maternal plasma for the development of a NIPD assay for β-thalassaemia. Objective To develop a sensitive, specific, simple, cost-effective and reproducible platform for the non-invasive prenatal detection of paternally inherited alleles for β-thalassaemia. The development of such an assay is of major significance in order to replace currently-applied invasive methods containing inherent fetal loss risks. Methods We present a fast Temperature-Gradient Co-amplification at Lower Denaturation Temperature Polymerase Chain Reaction (fast TG COLD PCR) methodology for the detection of the paternally-inherited fetal alleles in maternal plasma. Two single-nucleotide polymorphisms (SNPs), rs7480526 (G/T) and rs968857 (G/A) that are located on the β-globin gene cluster and exhibit a high degree of heterozygosity in the Cypriot population were selected for evaluation. Seventeen maternal plasma samples from pregnancies at risk for β-thalassemia were analysed for the selected SNPs using the novel fast TG COLD PCR assay. Results Using fast TG COLD PCR, the paternally inherited allele in cell free fetal DNA was correctly determined for all the 17 maternal plasma samples tested, showing full agreement with the Chorionic Villus Sampling (CVS) analysis. Conclusions Our findings are encouraging and demonstrate the efficiency and sensitivity of fast TG COLD PCR in detecting the minor paternally-inherited fetal alleles in maternal plasma for the development of a NIPD assay for β-thalassaemia. OBJECTIVETo develop a sensitive, specific, simple, cost-effective and reproducible platform for the non-invasive prenatal detection of paternally inherited alleles for β-thalassaemia. The development of such an assay is of major significance in order to replace currently-applied invasive methods containing inherent fetal loss risks.METHODSWe present a fast Temperature-Gradient Co-amplification at Lower Denaturation Temperature Polymerase Chain Reaction (fast TG COLD PCR) methodology for the detection of the paternally-inherited fetal alleles in maternal plasma. Two single-nucleotide polymorphisms (SNPs), rs7480526 (G/T) and rs968857 (G/A) that are located on the β-globin gene cluster and exhibit a high degree of heterozygosity in the Cypriot population were selected for evaluation. Seventeen maternal plasma samples from pregnancies at risk for β-thalassemia were analysed for the selected SNPs using the novel fast TG COLD PCR assay.RESULTSUsing fast TG COLD PCR, the paternally inherited allele in cell free fetal DNA was correctly determined for all the 17 maternal plasma samples tested, showing full agreement with the Chorionic Villus Sampling (CVS) analysis.CONCLUSIONSOur findings are encouraging and demonstrate the efficiency and sensitivity of fast TG COLD PCR in detecting the minor paternally-inherited fetal alleles in maternal plasma for the development of a NIPD assay for β-thalassaemia. |
Author | Kleanthous, Marina Christofides, Agathoklis Papasavva, Thessalia Makrigiorgos, G Mike Kallikas, Ioannis Byrou, Stefania |
AuthorAffiliation | 4 Medical Centre Fetal Medicine Department, Archbishop Makarios III Hospital, Nicosia, Cyprus 2 The Cyprus School of Molecular Medicine, Nicosia, Cyprus 1 Molecular Genetics Thalassaemia Department, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus 5 Ultrasound and fetal medicine centre, Nicosia, Cyprus 3 Department of Radiation Oncology, Division of Medical Physics & Biophysics, Dana Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, United States of America Defense Threat Reduction Agency, UNITED STATES |
AuthorAffiliation_xml | – name: Defense Threat Reduction Agency, UNITED STATES – name: 1 Molecular Genetics Thalassaemia Department, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus – name: 4 Medical Centre Fetal Medicine Department, Archbishop Makarios III Hospital, Nicosia, Cyprus – name: 5 Ultrasound and fetal medicine centre, Nicosia, Cyprus – name: 3 Department of Radiation Oncology, Division of Medical Physics & Biophysics, Dana Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, United States of America – name: 2 The Cyprus School of Molecular Medicine, Nicosia, Cyprus |
Author_xml | – sequence: 1 givenname: Stefania surname: Byrou fullname: Byrou, Stefania organization: The Cyprus School of Molecular Medicine, Nicosia, Cyprus – sequence: 2 givenname: G Mike surname: Makrigiorgos fullname: Makrigiorgos, G Mike organization: Department of Radiation Oncology, Division of Medical Physics & Biophysics, Dana Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, United States of America – sequence: 3 givenname: Agathoklis surname: Christofides fullname: Christofides, Agathoklis organization: Medical Centre Fetal Medicine Department, Archbishop Makarios III Hospital, Nicosia, Cyprus – sequence: 4 givenname: Ioannis surname: Kallikas fullname: Kallikas, Ioannis organization: Ultrasound and fetal medicine centre, Nicosia, Cyprus – sequence: 5 givenname: Thessalia orcidid: 0000-0001-9279-4810 surname: Papasavva fullname: Papasavva, Thessalia organization: The Cyprus School of Molecular Medicine, Nicosia, Cyprus – sequence: 6 givenname: Marina surname: Kleanthous fullname: Kleanthous, Marina organization: The Cyprus School of Molecular Medicine, Nicosia, Cyprus |
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CitedBy_id | crossref_primary_10_1016_j_jmoldx_2019_02_010 crossref_primary_10_1038_s41598_020_77084_0 crossref_primary_10_1039_C9CC04161C crossref_primary_10_1016_j_jmoldx_2024_04_002 crossref_primary_10_1093_clinchem_hvac076 |
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Snippet | To develop a sensitive, specific, simple, cost-effective and reproducible platform for the non-invasive prenatal detection of paternally inherited alleles for... Objective To develop a sensitive, specific, simple, cost-effective and reproducible platform for the non-invasive prenatal detection of paternally inherited... OBJECTIVETo develop a sensitive, specific, simple, cost-effective and reproducible platform for the non-invasive prenatal detection of paternally inherited... OBJECTIVE:To develop a sensitive, specific, simple, cost-effective and reproducible platform for the non-invasive prenatal detection of paternally inherited... Objective To develop a sensitive, specific, simple, cost-effective and reproducible platform for the non-invasive prenatal detection of paternally inherited... |
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SubjectTerms | Alleles Assaying beta-Thalassemia - diagnosis beta-Thalassemia - genetics Biology and Life Sciences Blood diseases Cancer Cell-Free Nucleic Acids - analysis Cell-Free Nucleic Acids - blood Cold Congenital diseases Denaturation Deoxyribonucleic acid DNA Drug dosages Female Fetuses Gene Frequency Genetic testing Genetics Genotyping Techniques Haplotypes Heterozygosity Humans Medical diagnosis Medicine Medicine and Health Sciences Methods Mutation Neurology Paternal Inheritance Plasma Polymerase chain reaction Polymerase Chain Reaction - methods Polymorphism, Single Nucleotide Pregnancy Prenatal diagnosis Prenatal Diagnosis - methods Research and Analysis Methods Risk analysis Sensitivity and Specificity Single-nucleotide polymorphism Temperature Temperature effects Thalassemia Villus |
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Title | Fast Temperature-Gradient COLD PCR for the enrichment of the paternally inherited SNPs in cell free fetal DNA; an application to non-invasive prenatal diagnosis of β-thalassaemia |
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