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Development of a duplex qPCR assay with locked nucleic acid probes for A, B and E kappa-casein variants detection

Milk proteins determine important milk technological characteristics. Among caseins, Ƙ-casein has been correlated with fat and protein content and cheese yield. Fourteen Ƙ-caseins variants have been described but the alleles A, B and E are the most important ones due to their frequency and/or influe...

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Autores principales: Jiménez-Montenegro, L., Mendizabal, J. A., Alfonso, L., Azparren, L., Urrutia, O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9525573/
https://www.ncbi.nlm.nih.gov/pubmed/36180500
http://dx.doi.org/10.1038/s41598-022-20586-w
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author Jiménez-Montenegro, L.
Mendizabal, J. A.
Alfonso, L.
Azparren, L.
Urrutia, O.
author_facet Jiménez-Montenegro, L.
Mendizabal, J. A.
Alfonso, L.
Azparren, L.
Urrutia, O.
author_sort Jiménez-Montenegro, L.
collection PubMed
description Milk proteins determine important milk technological characteristics. Among caseins, Ƙ-casein has been correlated with fat and protein content and cheese yield. Fourteen Ƙ-caseins variants have been described but the alleles A, B and E are the most important ones due to their frequency and/or influence on the technological aptitudes of milk. Therefore, in the present study two different duplex qPCR assays with locked nucleic acid probes (for positions 13104 and 13124 of the Ƙ-casein gene) were developed for the detection of A, B and E variants. Firstly, DNA isolation method from milk somatic cells and hair was optimised. The developed 13124-qPCR assay showed an increased sensitivity reaching up to 6.7 copies DNA copies/reaction at a 95% confidence level with A, B and E alleles reference samples. The 13104-qPCR assay reached up to 6.7 DNA copies/reaction for A allele reference sample and 67 DNA copies/reaction for B and E samples. Intra-assay variation results were below 6%. Applicability was determined using DNA samples from animals with known genotype for Ƙ-casein (AA, AB, BB, BE, AE, EE) and both assays were able to discriminate among the six genotypes with 100% accuracy. Thus, this qPCR method represents a sensitive and rapid option for the detection of Ƙ-casein alleles in both hair and milk samples.
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spelling pubmed-95255732022-10-02 Development of a duplex qPCR assay with locked nucleic acid probes for A, B and E kappa-casein variants detection Jiménez-Montenegro, L. Mendizabal, J. A. Alfonso, L. Azparren, L. Urrutia, O. Sci Rep Article Milk proteins determine important milk technological characteristics. Among caseins, Ƙ-casein has been correlated with fat and protein content and cheese yield. Fourteen Ƙ-caseins variants have been described but the alleles A, B and E are the most important ones due to their frequency and/or influence on the technological aptitudes of milk. Therefore, in the present study two different duplex qPCR assays with locked nucleic acid probes (for positions 13104 and 13124 of the Ƙ-casein gene) were developed for the detection of A, B and E variants. Firstly, DNA isolation method from milk somatic cells and hair was optimised. The developed 13124-qPCR assay showed an increased sensitivity reaching up to 6.7 copies DNA copies/reaction at a 95% confidence level with A, B and E alleles reference samples. The 13104-qPCR assay reached up to 6.7 DNA copies/reaction for A allele reference sample and 67 DNA copies/reaction for B and E samples. Intra-assay variation results were below 6%. Applicability was determined using DNA samples from animals with known genotype for Ƙ-casein (AA, AB, BB, BE, AE, EE) and both assays were able to discriminate among the six genotypes with 100% accuracy. Thus, this qPCR method represents a sensitive and rapid option for the detection of Ƙ-casein alleles in both hair and milk samples. Nature Publishing Group UK 2022-09-30 /pmc/articles/PMC9525573/ /pubmed/36180500 http://dx.doi.org/10.1038/s41598-022-20586-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Jiménez-Montenegro, L.
Mendizabal, J. A.
Alfonso, L.
Azparren, L.
Urrutia, O.
Development of a duplex qPCR assay with locked nucleic acid probes for A, B and E kappa-casein variants detection
title Development of a duplex qPCR assay with locked nucleic acid probes for A, B and E kappa-casein variants detection
title_full Development of a duplex qPCR assay with locked nucleic acid probes for A, B and E kappa-casein variants detection
title_fullStr Development of a duplex qPCR assay with locked nucleic acid probes for A, B and E kappa-casein variants detection
title_full_unstemmed Development of a duplex qPCR assay with locked nucleic acid probes for A, B and E kappa-casein variants detection
title_short Development of a duplex qPCR assay with locked nucleic acid probes for A, B and E kappa-casein variants detection
title_sort development of a duplex qpcr assay with locked nucleic acid probes for a, b and e kappa-casein variants detection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9525573/
https://www.ncbi.nlm.nih.gov/pubmed/36180500
http://dx.doi.org/10.1038/s41598-022-20586-w
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