Drosophila Lab Report

A) Their F1 offspring were 97 wild type quahaug flies. What is the genotype of these F1 flies??

It is also possible that a number of other random experimental errors (not mentioned above) affected the results of this experiment (for example the possible death of flies and their offspring due to mites and mould). These random errors could also be overcome by doing a large number of trials using a larger number of flies than used in this experiment.

The parents are both homozygous. The homozygous dominant would represent the wild type. And the homozygous recessive would represent the other fly parent of a different strain. The F1 generation would consist of 100% Wild Type but they would all be heterozygous in carrying the recessive gene.

Introduction: The intention of this lab was to gain a better understanding of Mendelian genetics and inheritance patterns of the drosophila fruit fly. This was tasked through inspecting phenotypes present in the dihybrid crosses performed on the flies. An experimental virtual fly lab assignment was also used to analyze the inheritance patterns. Specifically, the purpose of our drosophila crosses is to establish which phenotypes are dominant/recessive, if the traits are inherited through autosome or sex chromosomes and whether independent assortment or linkage is responsible for the expressed traits.

The motivation of this lab report is to use Mendel’s Laws of Inheritance to analyze and predict the genotypes and phenotypes of an offspring generation (F2) after knowing the genotypes and phenotypes of the parent generation (F1). The hypothesis for this experiment is that the mode of inheritance for the shaven bristle allele in flies is autosomal recessive in both male and female flies.

It would be expected that the mutant F1 flies would be heterozygous for the allele responsible for the grounded trait. If two F1 flies were mated, the percentage of flies that would be expected to be wildtype in the F2 generation would be 25% mutants given that the mutant allele (ap) is predicted to be recessive and, leaving 75% to be wildtype (ap+).

Flies may escape vials during experiment. Due to their small size, they should not cause significant harm if accidentally swallowed. Precaution should be taken to reduce likelihood of impacting the local ecosystem if significant amounts of flies are

There were eight different phenotypes among the progeny. The highest phenotypic frequency was the w+m+f+ at 40% of the progeny. The lowest was the w+mf+ with only 2 % of the progeny (Table 3). The sum of the recombinant frequencies between genes, table 4, was used to determine the gene distance. The recombinant frequency was determined by counting the number of individuals whose genes differed from that of the parental type. For example, how many individuals white eye gene, and miniature wing gene, differed from both wild-type or both mutants. Recombination occurred between the white and miniature gene 33 times. Recombination occurred between the miniature and the forked genes 31 times. Recombination occurred between the white and forked genes 44 time. Double recombination occurred 10 times. Therefore, genes w and f are 64 m.u. apart, m and w are 33 m.u. apart, and m and f are 31 m.u. apart (Figure

Two sepia virgin drosophila females and five, dumpy drosophila are put in a vial containing agar. Nap was used to anesthetize the flies. After a week f1 had laid eggs and f1 pupas were visible. Parents were removed from vial. A week later the drosophila f1 had developed and were analyzed and counted.

Heterozygotes, which have the wild type phenotype, have normal sight which gives them the advantage of finding a mate and have a better success with attracting a mate with their courtship song (Kyriacou et al, 1978). The male heterozygous Drosophila had a better advantage at mating than the homozygotes, which were the ebony, and therefore we predict there will be more wild type by the end of the experiment.

The Drosophila melanogaster is a fruit fly with a very short life cycle. They can be winged or wingless, and have red eyes or white eyes. The different options are called alleles. Alleles are the variants of a specific gene, and one is received from each parent on each chromosome. (“What Are Dominant and Recessive?”). It was chosen to use winged females and wingless males to predict the offspring in this experiment. The winged allele is dominant, meaning it only needs one allele to physically appear. The wingless allele is recessive, which gets covered up by the dominant allele (“Fruit Fly Genetics”). Each trait has two alleles in the flies’

we said goodbye and placed them in the fly morgue. We allowed the F2 larval

For our first generation (F1) of flies we chose to cross apterous (+) females and white-eye (w) males. We predicted that the mutation would be sex linked recessive. So if the female was the sex with the mutation then all females would be wild type heterozygous. Heterozygous is a term used when the two genes for a trait are opposite. The males would all be white eye since they only have one X chromosome. If the males were the sex that had the mutation then all the flies would be wild type but the females would be heterozygous.

The study of population genetics is simply how the genes or alleles within a population may vary or change. The purpose of population genetics is being able to predict the genes that are expressed in future generations and understanding why that is. An allele is an alternate form of a gene, so blonde hair and black hair are both alleles but hair color is a gene. In this particular experiment the alleles being focused on are the body colors of the Drosophila melanogaster, which is the common fruit fly. The two different body color alleles are the wild type, tan body color, and the ebony type, black body color.

This experiment looks at the relationship between genes, generations of a population and if genes are carried from one generation to another. By studying Drosophila melanogaster, starting with a parent group we crossed a variety of flies and observe the characteristics of the F1 generation. We then concluded that sex-linked genes and autosomal genes could indeed be traced through from the parent generation to the F1 generation.