As a contribution to DUS testing within the system of protection of plant breeders' rights (PBR), the AFLP molecular system has been used in this study to produce DNA fingerprinting profiles. DNA polymorphism and genetic distance of nine agronomicaly important maize genotypes has been investigated using the AFLP technique. Two specific adapters, two preselective primers and twenty selective primers were utilized for DNA amplification. The selective primers were GC rich, each having a 3-mer selective sequence at 3' termini. Ten double stranded primer combinations were made out of the twenty primers but only five of them turned out to be reliable. Out of 253 amplified DNA fragments, 177 were polymorphic (70%). The CGA/GAG (B) primer combination has proved to be the most polymorphic (44 polymorphic fragments have been recorded) revealing the polymorphism rate of 81.5%. Genotypes g1 and g7 were most distinct (GD=55% and GD=79%, respectively) and genotypes g1. g4 and g8 were closest (GD=55% in all cases). The paper discusses possible uses of AFLP DNA profiling technique to achieve a unique fingerprinting pattern of agronomicaly important maize genotypes
Maize is one of the most important economic crops and the best studied and most tractable genetic system among monocots. The development of biotechnology has led to a great increase in our knowledge of maize genetics and understanding of the structure and behaviour of maize genomes. Conventional breeding practices can now be complemented by a number of new and powerful techniques. Some of these often referred to as molecular methods, enable scientists to see the layout of the entire genome of any organism and to select plants with preferred characteristics by "reading" at the molecular level, saving precious time and resources. DNA markers have provided valuable tools in various analyses ranging from phylogenetic analysis to the positional cloning of genes. Application of molecular markers for genetic studies of maize include: assessment of genetic variability and characterization of germ plasm, identification and fingerprinting of genotypes, estimation of genetic distance, detection of monogamic and quantitative trait loci, marker assisted selection, identification of sequence of useful candidate genes, etc. The development of high-density molecular maps which has been facilitated by PCR-based markers, have made the mapping and tagging of almost any trait possible and serve as bases for marker assisted selection. Sequencing of maize genomes would help to elucidate gene function, gene regulation and their expression. Modern biotechnology also includes an array of tools for introducing or deieting a particular gene or genes to produce plants with novel traits. Development of informatics and biotechnology are resulted in bioinformatic as well as in expansion of microarrey technique. Modern biotechnologies could complement and improve the efficiency of traditional selection and breeding techniques to enhance agricultural productivity
The objective of this paper was to examine the functionality of two microsatellite primers as their polymorphism levels were determined for select Novi Sad wheat genotypes. Chosen as representatives of Gater-sleben wheat microsatellites (GWM) were two sets of microsatellite primers, GWM 165 and GWM539, which had been described according to RODER et al. (1998a; 1998b). Twenty five wheat genotypes from the World Collection of the Institute of Field and Vegetable Crops in Novi Sad were used in the study. Genomic DNA was isolated from the plant materials using a modification of the PLASCHKE et al. (1995) method. PCR amplification of the desired fragments was carried out in a volume of 30 ul (Eppendorf thermocycler) according to RODER et al. (1998b). The PAGE conditions were implemented according to GALOV1Ć et al. (2004). The GWM539 set, with six different alleles, showed a higher level of polymorphism than GWM165, in which three different alleles were detected for the locus concerned
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