Literature DB >> 26843017

Development of Novel High-Resolution Melting-Based Assays for Genotyping Two Alu Insertion Polymorphisms (FXIIIB and PV92).

Yeimy González-Giraldo1,2, Marisol Rodríguez-Dueñas2,3, Diego A Forero4.   

Abstract

Insertion/Deletion polymorphisms (InDels) are a common type of genetic variation, with a growing role in population genetics and applied genomics. There is the need for the development of novel cost-effective assays for genotyping InDels of high importance. The main objective of this study was to develop high-resolution melting-based assays for genotyping two commonly studied Alu insertion polymorphisms: FXIIIB and PV92 (rs70942849 and rs3138523). Three primers (two forward and one reverse) were designed for each marker, and high-resolution melting (HRM) analyses in a qPCR platform were performed, using EvaGreen fluorescent dye. For each one of the two Alu insertion polymorphisms, HRM analyses identified distinguishable peaks for the three genotypes, allowing a robust genotyping. Results were validated using 96 DNA samples previously genotyped and the assays worked with different DNA concentrations. In this study, we developed novel cost-effective assays, using qPCR, for genotyping two Alu insertion polymorphisms (widely used as ancestry markers). Our results highlight the feasibility of using HRM analyses for genotyping InDel polymorphisms of medical and biotechnological importance.

Entities:  

Keywords:  Ancestry informative markers; Genotyping assays; High-resolution melting; Insertion/Deletion polymorphisms; Molecular genetics; Real-time PCR

Mesh:

Substances:

Year:  2016        PMID: 26843017     DOI: 10.1007/s12033-016-9915-4

Source DB:  PubMed          Journal:  Mol Biotechnol        ISSN: 1073-6085            Impact factor:   2.695


  33 in total

1.  A validation study of the Qiagen Investigator DIPplex® kit; an INDEL-based assay for human identification.

Authors:  Bobby L LaRue; Jianye Ge; Jonathan L King; Bruce Budowle
Journal:  Int J Legal Med       Date:  2012-01-15       Impact factor: 2.686

2.  Automating resequencing-based detection of insertion-deletion polymorphisms.

Authors:  Tushar R Bhangale; Matthew Stephens; Deborah A Nickerson
Journal:  Nat Genet       Date:  2006-11-19       Impact factor: 38.330

Review 3.  High-resolution melting: applications in genetic disorders.

Authors:  Tze-Kiong Er; Jan-Gowth Chang
Journal:  Clin Chim Acta       Date:  2012-09-18       Impact factor: 3.786

4.  Phylogenetics of worldwide human populations as determined by polymorphic Alu insertions.

Authors:  Gabriela Antunez-de-Mayolo; Adriana Antunez-de-Mayolo; Pamela Antunez-de-Mayolo; Surinder S Papiha; Michael Hammer; Juan J Yunis; Emilio J Yunis; Chendi Damodaran; Marian Martinez de Pancorbo; Jose Luis Caeiro; Valery P Puzyrev; Rene J Herrera
Journal:  Electrophoresis       Date:  2002-09       Impact factor: 3.535

5.  A functional polymorphism in the promoter region of MAOA gene is associated with daytime sleepiness in healthy subjects.

Authors:  Diego A Ojeda; Carmen L Niño; Sandra López-León; Andrés Camargo; Ana Adan; Diego A Forero
Journal:  J Neurol Sci       Date:  2013-12-11       Impact factor: 3.181

6.  A novel association of two non-synonymous polymorphisms in PER2 and PER3 genes with specific diurnal preference subscales.

Authors:  Diego A Ojeda; Claudia S Perea; Carmen L Niño; Rafael M Gutiérrez; Sandra López-León; Humberto Arboleda; Andrés Camargo; Ana Adan; Diego A Forero
Journal:  Neurosci Lett       Date:  2013-08-19       Impact factor: 3.046

7.  Detailed analysis of the serotonin transporter gene (SLC6A4) shows no association with bipolar disorder in the Northern Swedish population.

Authors:  Maaike Alaerts; Shana Ceulemans; Diego Forero; Lotte N Moens; Sonia De Zutter; Lien Heyrman; An-Sofie Lenaerts; Karl-Fredrik Norrback; Dirk Goossens; Peter De Rijk; Lars-Göran Nilsson; Rolf Adolfsson; Jurgen Del-Favero
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2009-06-05       Impact factor: 3.568

8.  PCR detection of the insertion/deletion polymorphism of the human angiotensin converting enzyme gene (DCP1) (dipeptidyl carboxypeptidase 1).

Authors:  B Rigat; C Hubert; P Corvol; F Soubrier
Journal:  Nucleic Acids Res       Date:  1992-03-25       Impact factor: 16.971

9.  Scoring insertion-deletion polymorphisms by dynamic allele-specific hybridization.

Authors:  Sarah L Sawyer; W Mathias Howell; Anthony J Brookes
Journal:  Biotechniques       Date:  2003-08       Impact factor: 1.993

10.  An integrated map of genetic variation from 1,092 human genomes.

Authors:  Goncalo R Abecasis; Adam Auton; Lisa D Brooks; Mark A DePristo; Richard M Durbin; Robert E Handsaker; Hyun Min Kang; Gabor T Marth; Gil A McVean
Journal:  Nature       Date:  2012-11-01       Impact factor: 49.962

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  1 in total

Review 1.  Does Genetic Predisposition Contribute to the Exacerbation of COVID-19 Symptoms in Individuals with Comorbidities and Explain the Huge Mortality Disparity between the East and the West?

Authors:  Naoki Yamamoto; Rain Yamamoto; Yasuo Ariumi; Masashi Mizokami; Kunitada Shimotohno; Hiroshi Yoshikura
Journal:  Int J Mol Sci       Date:  2021-05-08       Impact factor: 5.923

  1 in total

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