The importance of this experimental study cannot be disregarded. This is because of its scientific weight to researchers about solving the life challenges of human beings that revolve around the DNA structure and composition.In brief, the fundamental materials that were used in the study include the wrinkled mutant fruit fly, eleven other mutant strains and laboratory equipment, i.e. CO2 Tank and controller, vials, foodstuffs, dried yeast, dispensing jar, dissembler microscopes, paintbrushes, forceps, sharpies sorting boxes and fly morgue.From the experiment, it is evident that ten genes are available in the region. Under the associated gene name, the gene represented by wrinkled gene w is not present based on the results from the BLAST link provided. It is therefore found outside the genus Drosophila. The starting hypothesis is, therefore, rejected. It is prominent that the most unexpected thing occurred in the experimental results. The fact that the gene location of W that was under investigation was not available from the genome database indicates that the identical chromosomes of the Drosophila fruit fly would theoretically never recombine. This is predominantly because, the diploid characteristic of chromosomes permits for genes on dissimilar chromosomes to separate, independently, or be separated from their homologous pair throughout sexual reproduction in which haploid gametes are produced.Drosophila melanogaster is a variety of fly in the taxonomic order Diptera, family Drosophilidae. It is commonly referred to as fruit fly. It is a biological research model in diverse fields ranging from heredity studies, physiological studies, and microbial pathogenesis to life account evolution. This species of fly is preferred by researchers because it is easy to maintain, has four pairs in terms of chromosomal composition, breeds faster due to its characteristic shorter lifespan, and possesses higher fecundity levels. Thus, the essence of this paper is to explore the genetic mapping of the fruit fly concerning gene mutation and recombination in the chromosomal sites. Additionally, the determination of sex linkage and auto somatic linkage are ideally fundamental (Alice, 2).
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