Authors: I. O. Daniel, J. A. Adetumbi, O. O. Oyelakin, S. A. Olakojo, M. O. Ajala, S. O. Onagbesan
American Journal of Experimental Agriculture, 2(4): 597-606, 2012
Abstract
Aims: Morphological evaluation of seeds and growing plants used for certification for purity and variety distinctness in Nigeria is time consuming and expensive. This experiment set to evaluate the usefulness of SSR markers to determine genetic purity of commercial hybrids and their inbred lines.
Place and Duration of Study: Bioscience unit, International Institute of Tropical Agriculture, Nigeria in December, 2011
Methodology: Seedlings of four F1 hybrids and four inbred lines were grown in the screen house of IITA for DNA extraction using Dellaporta method with some modifications. Six Simple Sequence Repeat (SSR) markers were used for Polymerase Chain Reaction (PCR) using Touch-Down PCR profile. The analysis is by fragment analysis as present (1) or absent (0) Mathematical equation to determine genetic purity of the genotypes was developed from the genetic distances matrix.
Results: Simple descriptive analysis revealed that average genetic diversity and
polymorphism information content (PIC) recorded by the markers was 0.592 and 0.512 respectively. Genetic purity level of inbred lines ranged between 91.3% and 98.7% while the hybrids ranged between 81.3% and 95%.
Conclusion: SSR markers are powerful biotechnological tool capable of detecting genetic purity status of Nigerian maize hybrids therefore inclusion of DNA analysis of seeds using SSR markers to determine genetic purity of maize seed is recommended. However, further research work with larger number of seed samples per variety will be needed to validate reliability.
Keywords: Maize; genetic purity; DNA analysis; SSR markers.