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Utilization of SSR Markers to Identify Slow Rusting Genes in Spring Wheat (Triticum aestivum L.)
Author(s):
1. Ghassan Zahid: Department of Biotechnology, The University of Azad Jammu and Kashmir,Muzafarabad,Pakistan
2. Sania Begum: Department of Plant Genomics and Biotechnology, National Agricultural Research Centre,Islamabad, Pakistan
3. Sikandar Almani: Department of Chemical Engineering, Mehran University of Engineering and Technology,Jamshoro,Pakistan
4. Sahir Hameed Khattak: Department of Plant Genomics and Biotechnology, National Agricultural Research Centre,Islamabad,Pakistan
5. Rajesh Kumar Soothar: Faculty of Agricultural Engineering, Sindh Agriculture University,Tandojam,Pakistan
6. Shakeel Ahmed Soomro: Faculty of Agricultural Engineering, Sindh Agriculture University,Tandojam,Pakistan
Abstract:
| The virulence of rust diseases in wheat crop like leaf, stripe and stem-rust declines the grain quality and productivity. Cultivars having a durable rust resistance is an effective method to control the spread of rust disease in cereal crops particularly in wheat. The experiment was conducted on fifty-two wheat lines comprised of forty-five double haploids of wheat along with seven wheat genotypes. Besides that, three positive checks and three SSR primers were also included in the study to check the durability i.e. Opata-85 Sr2/Lr27check, Pavon-76 (Yr-29/Lr-46) and Tukuru (Yr18/Lr34) respectively. The molecular markers screening results indicated that the primer Sr2/Lr27 was present in almost all of the double haploids and genotypes except the Nesser and Tukuru varieties. The Yr29/Lr46 gene complex was present in all double haploids and genotypes except for Nesser, Opata-85, inqilab-91 and Tukuru. the gene complex Yr18/Lr34 was present in eight double haploids, and only one genotype showed its presence, however the rest of the genotypes lacked this gene complex. The obtained results intimated that the 8 double haploids 33, 34, 44, 45, 46, 48, 53, 54, and genotype weebil-1 contained all the slow rusting genes complex i.e. Yr18/Lr34, Yr29/ Lr46 and Sr2/Lr27. Therefore, detection of slow rusting gene complex in these varieties with the assistance of molecular markers can be utilized for slow-rust resistance. Furthermore, the selected markers can be used as a primary choice for detecting rust resistance genes specifically in the wheat breeding population.
Page(s): 85-92
DOI: DOI not available
Published: Journal: Pakistan Journal of Agricultural Research, Volume: 35, Issue: 1, Year: 2022
Keywords:
molecular markers , rust diseases , wheat , Simple sequence repeats , Durable rust resistance
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