Genetic analysis of wild and cultivated germplasm of pigeonpea using random amplified polymorphic DNA (RAPD) and simple sequence repeats (SSR) markers

  • Babasaheb Walunjkar
  • Akarsh Parihar
  • Pratibha Chaurasia
  • K Pachchigar
  • RM Chauhan

Abstract

The reliability of the quantification of genetic diversity using only one type of marker has been questioned as compared to the combined use of different markers. To compare the efficiency of the use of single versus multiple markers, the genetic diversity was quantified among 12 diverse pigeonpea germplasm comprised of eight wild and four cultivated using both random amplified polymorphic DNA (RAPD) and simple sequence repeat (SSR) markers, and how well these two types of markers discriminated the diverse pigeonpea germplasm was evaluated. The pigeonpea germplasm including eight wild species and four cultivated varieties was subjected to 40 RAPD and 40 microsatellite primers. The level of polymorphism as revealed by RAPD primers produced a total of 517 DNA fragments and all were found to be polymorphic that is, 100% and in SSR analysis 101 fragments were produced that too showed 100% polymorphism. The high similarity index value revealed by RAPD was 0.931 between GT-100 and ICPL-87 whereas through SSR, it was 1.00 between GTH-1 and GT-100 as well as Rhyncosia rothi and Rhyncosia minima. The least similarity index value revealed by RAPD (R. rothi and GTH-1) and SSR (Rhyncosia bracteata and ICPL-87) were 0.07 and 0.133, respectively. Using RAPD marker, the calculated arithmetic mean heterozygosity and the marker index were 0.90 and 22.47, respectively. The R. bracteata and ICPL-87 were found distinct from rest of other cultivars by showing only 13% similarity. Average PIC value shown by RAPD and SSR primers were found to be 0.90 and 0.18, respectively.

Keywords: Pigeonpea, random amplified polymorphic DNA (RAPD), simple sequence repeats (SSR) markers.

African Journal of Biotechnology Vol. 12(40), pp. 5823-5832

Author Biographies

Babasaheb Walunjkar
Department of Plant Molecular Biology and Biotechnology, S. D. Agricultural University, S.K. Nagar, Gujarat, India.
Akarsh Parihar
Centre of excellence, Department of Agricultural Biotechnology, Anand Agricultural University, Anand-388110, Gujarat, India
Pratibha Chaurasia
Department of Biotechnology, Genetics and Bioinformatics, N.V. Patel College of Pure and Applied Sciences, S.P. University, V.V.Nagar-388120, Gujarat, India
K Pachchigar
Department of Plant Molecular Biology and Biotechnology, S. D. Agricultural University, S.K. Nagar, Gujarat, India.
RM Chauhan
Department of Plant Molecular Biology and Biotechnology, S. D. Agricultural University, S.K. Nagar, Gujarat, India.
Published
2016-06-03
Section
Articles

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eISSN: 1684-5315