Literature DB >> 31975323

Rapid genotyping of F8 intron 22 inversion by nested PCR based on long-distance PCR.

Xiong Wang1, Weihong Hu1, Yong Gao2, Dengju Li3, Yanjun Lu4.   

Abstract

F8 intron 22 inversion (Inv22) accounts for about 40% of severe hemophilia A (HA) cases and is mainly genotyped by long-distance PCR (LD-PCR) or inverse-PCR (I-PCR). These methods require long separation times or enzymatic digestion. We aimed to shorten the separation time of LD-PCR. Long-read sequencing was applied for LD-PCR products from 20 Inv22 patients and 4 controls to validate the differences between products generated using P-Q and P-B primer pairs in LD-PCR. We then confirmed two unique regions (chrX: 154879481-154880814, chrX: 155376388-155376505, GRCh38) in the PCR products from P-Q and P-B primer pairs, respectively. The nested PCR P1, Q1, and B1 primers were located near the homologous sequence and two unique regions, respectively. The P1-Q1 and P1-B1 primer pairs generated 1621 bp and 540 bp fragments, respectively, and the Inv22 carriers produced both fragments. In total, 228 previously diagnosed subjects including 39 Inv22 carriers, 52 Inv22 patients, 82 Inv22 negative males, and 55 Inv22 negative females were genotyped using nested PCR, and the results revealed excellent sensitivity and specificity (100 and 100%, respectively). The separation time was shortened from 5 to 0.5 h. Therefore, we present a rapid genotyping method for F8 Inv22 by nested PCR based on LD-PCR.

Entities:  

Keywords:  F8 intron 22 inversion; Hemophilia A; Long-distance PCR; Long-read sequencing; Nested PCR

Mesh:

Substances:

Year:  2020        PMID: 31975323     DOI: 10.1007/s11239-020-02043-5

Source DB:  PubMed          Journal:  J Thromb Thrombolysis        ISSN: 0929-5305            Impact factor:   2.300


  17 in total

1.  Inverse PCR to perform long-distance haplotyping: main applications to improve preimplantation genetic diagnosis in hemophilia.

Authors:  Miguel Martín Abelleyro; Vanina Daniela Marchione; Micaela Palmitelli; Claudia Pamela Radic; Daniela Neme; Irene Beatriz Larripa; Enrique Medina-Acosta; Carlos Daniel De Brasi; Liliana Carmen Rossetti
Journal:  Eur J Hum Genet       Date:  2019-01-09       Impact factor: 4.246

2.  New protocol for detection of intron 22 inversion mutation from cases with hemophilia A.

Authors:  Praveen Kumar; Nuzhat Husain; Priyanka Soni; Nuzhat Jahan Faridi; Sudhir Kumar Goel
Journal:  Clin Appl Thromb Hemost       Date:  2013-09-19       Impact factor: 2.389

3.  Accurate, simple, and inexpensive assays to diagnose F8 gene inversion mutations in hemophilia A patients and carriers.

Authors:  Debargh Dutta; Devi Gunasekera; Margaret V Ragni; Kathleen P Pratt
Journal:  Blood Adv       Date:  2016-12-14

Review 4.  Haemophilia A: from mutation analysis to new therapies.

Authors:  Jochen Graw; Hans-Hermann Brackmann; Johannes Oldenburg; Reinhard Schneppenheim; Michael Spannagl; Rainer Schwaab
Journal:  Nat Rev Genet       Date:  2005-06       Impact factor: 53.242

5.  Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female.

Authors:  R Favier; J M Lavergne; J M Costa; C Caron; C Mazurier; M Viémont; M Delpech; S Valleix
Journal:  Blood       Date:  2000-12-15       Impact factor: 22.113

6.  Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A.

Authors:  D Lakich; H H Kazazian; S E Antonarakis; J Gitschier
Journal:  Nat Genet       Date:  1993-11       Impact factor: 38.330

Review 7.  Molecular etiology of factor VIII deficiency in hemophilia A.

Authors:  S E Antonarakis; H H Kazazian; E G Tuddenham
Journal:  Hum Mutat       Date:  1995       Impact factor: 4.878

8.  Preimplantation genetic diagnosis for hemophilia A using indirect linkage analysis and direct genotyping approaches.

Authors:  A D Laurie; A M Hill; J R Harraway; A P Fellowes; G T Phillipson; P S Benny; M P Smith; P M George
Journal:  J Thromb Haemost       Date:  2010-01-21       Impact factor: 5.824

9.  Long-read genome sequencing identifies causal structural variation in a Mendelian disease.

Authors:  Jason D Merker; Aaron M Wenger; Tam Sneddon; Megan Grove; Zachary Zappala; Laure Fresard; Daryl Waggott; Sowmi Utiramerur; Yanli Hou; Kevin S Smith; Stephen B Montgomery; Matthew Wheeler; Jillian G Buchan; Christine C Lambert; Kevin S Eng; Luke Hickey; Jonas Korlach; James Ford; Euan A Ashley
Journal:  Genet Med       Date:  2017-06-22       Impact factor: 8.822

10.  High-throughput annotation of full-length long noncoding RNAs with capture long-read sequencing.

Authors:  Julien Lagarde; Barbara Uszczynska-Ratajczak; Silvia Carbonell; Sílvia Pérez-Lluch; Amaya Abad; Carrie Davis; Thomas R Gingeras; Adam Frankish; Jennifer Harrow; Roderic Guigo; Rory Johnson
Journal:  Nat Genet       Date:  2017-11-06       Impact factor: 38.330

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.