Characterization of β‑lactoglobulin and κ‑casein genotypes PCR-RFLP in dairy cattle from Panama.

Brazilian journal of veterinary medicine Pub Date : 2026-07-24 eCollection Date: 2026-01-01 DOI:10.29374/2527-2179.bjvm001026
Anabel Argelis García, Jenyfer Pérez García, Dilcia Sambrano, Fermín Acosta, César Edwards, José Torres, Diomedes Trejos, Amador Goodridge, Cecilia Escobar
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Abstract

Sustained profitability in dairy production requires continuous improvements in milk yield and composition, traits that are strongly influenced by underlying genetic factors. Polymorphisms in the milk protein genes β-lactoglobulin (β-Lg) and κ-casein (κ-Cn) have been associated with variation in milk production, composition, and technological properties across dairy breeds. This study applied polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis to characterize β‑Lg and κ‑Cn gene variants in Jersey (JE), crossbred (XX), and Creole (CR) dairy cattle in Panama. Genotypic and allelic variation was evaluated using a convenience sample of 351 blood samples collected between 2014 and 2015 (JE, n = 230; XX, n = 90; CR, n = 26). Although the sampling strategy does not support population‑level inference, it is suitable for assessing the feasibility of PCR‑RFLP and conducting an exploratory characterization of genetic variability. Amplification success was 98.6% for β‑Lg and 76.6% for κ‑Cn. At the β‑Lg locus, allele A predominated in JE (0.55) and CR (0.52) cattle, whereas allele B was more frequent in XX cattle (0.73). At the κ‑Cn locus, allele B predominated across all groups. Overall, PCR‑RFLP proved to be a practical and accessible method for detecting variations in milk protein genes, supporting its application in future population‑based studies under Panamanian production conditions.

巴拿马奶牛β -乳球蛋白和κ -酪蛋白基因型PCR-RFLP分析
乳品生产的持续盈利需要不断改进产奶量和成分,这些性状受潜在遗传因素的强烈影响。乳蛋白基因β-乳球蛋白(β-Lg)和κ-酪蛋白(κ-Cn)的多态性与奶牛品种的产奶量、成分和技术特性的差异有关。本研究采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术对巴拿马泽西奶牛(JE)、杂交奶牛(XX)和克里奥尔奶牛(CR)的β‑Lg和κ‑Cn基因变异进行了分析。采用2014 - 2015年间采集的351份便捷血样(乙脑230份,XX 90份,CR 26份)评估基因型和等位基因变异。虽然采样策略不支持群体水平的推断,但它适用于评估PCR - RFLP的可行性,并对遗传变异进行探索性表征。β‑Lg和κ‑Cn的扩增成功率分别为98.6%和76.6%。在β - Lg位点,等位基因A在乙脑(0.55)和CR(0.52)牛中占主导地位,而等位基因B在XX牛中更常见(0.73)。在κ‑Cn位点,等位基因B在所有组中占主导地位。总的来说,PCR - RFLP被证明是检测牛奶蛋白基因变异的一种实用且容易获得的方法,支持其在未来巴拿马生产条件下基于种群的研究中的应用。
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