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Development of a novel SNP assay to detect lactase persistence associated genetic variants

BACKGROUND: In adulthood the activity of the lactase enzyme is inherited as autosomal dominant form associated to Single nucleotide polymorphisms (SNPs). The present research was aimed to develop a novel genetic method to test lactase non persistence more powerfully. METHODS AND RESULTS: In our stud...

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Detalles Bibliográficos
Autores principales: De Luca, Pasquale, Iaconis, Daniela, Biffali, Elio, Enza, Coluccia, de Magistris, Laura, Riegler, Gabriele, Pappalardo, Diego, Amato, Maria Rosaria, Iardino, Patrizia, Montanino, Concetta, De Felice, Bruna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572811/
https://www.ncbi.nlm.nih.gov/pubmed/34515921
http://dx.doi.org/10.1007/s11033-021-06698-y
Descripción
Sumario:BACKGROUND: In adulthood the activity of the lactase enzyme is inherited as autosomal dominant form associated to Single nucleotide polymorphisms (SNPs). The present research was aimed to develop a novel genetic method to test lactase non persistence more powerfully. METHODS AND RESULTS: In our study, we selected eight different SNPs that are associated with lactase persistence from Caucasian, Arabian Bedouins, sub-Saharian Africans and Asian populations to set up an approach to detect all the eight different SNPs at the same time in the same sample. This technique is centred on the identification of SNPs with a single nucleotide primer extension method using Sanger sequencing and capillary electrophoresis. CONCLUSIONS: Our method allowed us to check the genotype asset of eight SNPs related to lactase persistence simultaneously and in a very efficient manner. It could be applied to a higher number of SNPs in a single reaction.