PCR Optimization Based on Inter-Primer Binding Site (iPBS) Markers for Genetic Diversity Analysis in Durum Wheat Genotypes

In this study, PCR optimization was performed using iPBS (inter-primer binding site) molecular markers to determine the genetic diversity of durum wheat genotypes. Optimizing PCR conditions to enhance the efficiency of iPBS markers was a critical step. To improve the accuracy of the molecular analysis, gradient testing was conducted with 20 different iPBS primers to determine the optimum annealing temperatures. The results showed that 11 primers produced polymorphic bands, and the temperatures at which these primers bound most efficiently were identified. Correctly determining the annealing temperatures of the primers directly impacted the success of the PCR process, ensuring reliable DNA amplification.

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Publication Details

Journal
Erciyes Tarım ve Hayvan Bilimleri Dergisi
Published
2026-03-27
DOI
https://doi.org/10.55257/ethabd.1827396
Primary Topic
Genetic diversity and population structure
Type
article
Field-Weighted Citation Impact
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article

PCR Optimization Based on Inter-Primer Binding Site (iPBS) Markers for Genetic Diversity Analysis in Durum Wheat Genotypes

Seval Eliş, M. Serdar Yıldırım, Kamil Haliloğlu, BÜŞRA POLAT et al.
Erciyes Tarım ve Hayvan Bilimleri Dergisi
Genetic diversity and population structure
article

PCR Optimization Based on Inter-Primer Binding Site (iPBS) Markers for Genetic Diversity Analysis in Durum Wheat Genotypes

Seval Eliş, M. Serdar Yıldırım, Kamil Haliloğlu, BÜŞRA POLAT, Ferhat Kızılgeçi, Aras Türkoğlu
article en

Abstract

In this study, PCR optimization was performed using iPBS (inter-primer binding site) molecular markers to determine the genetic diversity of durum wheat genotypes. Optimizing PCR conditions to enhance the efficiency of iPBS markers was a critical step. To improve the accuracy of the molecular analysis, gradient testing was conducted with 20 different iPBS primers to determine the optimum annealing temperatures. The results showed that 11 primers produced polymorphic bands, and the temperatures at which these primers bound most efficiently were identified. Correctly determining the annealing temperatures of the primers directly impacted the success of the PCR process, ensuring reliable DNA amplification.

Erciyes Tarım ve Hayvan Bilimleri DergisiVol. 9
Dicle University (TR), Mardin Artuklu University (TR), Necmettin Erbakan University (TR), Gazi Hastanesi (TR), Atatürk University (TR)
Openalex Percentile: Top 6%
Genetic diversity and population structure
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