Abstract

Molecular diversity in thirty wheat genotypes was done. For this the genomic DNA isolation was carried out and which were then subjected to PCR amplification using twenty SSR primers. Out of these twenty SSR primers, eighteen yielded amplifications and showed polymorphism. Total 93 loci were generated by amplification with 18 polymorphic primers, all of which 93 loci were polymorphic i.e. 100%. Among the SSR primers, BARC-170, WMC-44, produced maximum number of 2 loci. The size of amplification products ranged from 102 bp to 805 bp. All SSR primers showed 100 % polymorphism and all primers had more than 0.50 PIC value except one primer. Maximum PIC value 0.17 was observed in WMC-468. The maximum number of bands were observed in NIAW-2721 (28 bands), whereas minimum number of bands were present in NIAW-301 and NIAW-2539 (19 bands). The dice similarity coefficient values ranged from 0.50 to 0.95. Maximum similarity value of 0.95 was noticed between NIAW-2891 and NIAW-2837, while minimum similarity value of 0.50 was observed among NIAW-2595, NIAW-2874, NIAW-2995 and NIAW-2725. The consensus tree software revealed two major clusters.

Highlights

  • Wheat is the foremost and strategic cereal crop of the world and is the most important and major staple food of more than thirty six percent of worlds population

  • The plant material for the study comprised of thirty three wheat genotypes, which were collected from Agriculture Research Station Niphad, District Nashik, Maharashtra

  • The seeds obtained were sown in plots inside poly house for genomic DNA isolation. Details of these wheat genotypes along with their pedigree are given in table 1

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Summary

Introduction

Wheat is the foremost and strategic cereal crop of the world and is the most important and major staple food of more than thirty six percent of worlds population. The present investigation was conducted to Characterize thirty three wheat genotypes (Triticum aestivum L.) by molecular methods. The clearly resolved PCR amplified bands of wheat genotypes with different SSR and ISSR primers were scored manually as binary matrix for their presence (1) and absence (0) in the data sheet. Molecular marker was used effectively in the assessment of genetic diversity in wheat.

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Conclusion

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