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Fruit fly experiment lab report
Fruit fly experiment lab report
Fruit fly experiment lab report
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Abstract:
This paper analyzes whether or not gene to map distance in Sordaria fimicola is affected by changes in environmental conditions. The main focus is on how temperature affects the recombination frequency in this organism. It is analyzed if under different environmental conditions wt x gray and wt x tan varies in their percent crossing over. It is investigated how factors such as temperature and ultraviolet light have affected the gene to centromere distance in Sordaria. Results obtained in lab as well as scientific researches prove that as temperatures increases the percent of crossing over increases as well.
Introduction:
Sordaria fimicola belongs to the kingdom of fungi and is part of the phylum Ascosmycota. This fungus habitat is in the feces of herbivores. As many fungi Sordaria have one life cycles which is haploid/ diploid. It is commonly exits as a haploid organism, but when the mycelium from two individuals meets, the result is a diploid zygote. This diploid zygote which undergoes meiosis forms eight haploid ascospores . The ability of Sordaria to make 8 haploid ascospores is what makes it unique and important for the laboratory exercise done in lab.
The laboratory performed had as a purpose to determine the change in crossing-over frequency or the also called map distance under different environmental conditions in Sordaria sp. This paper has a purpose to analyze with the help of scientific research the results obtained in the laboratory exercise. To investigate the crossing over in Sordaria sp., a cross between two mutant strains was performed. The mutant strains used had different genes for spore color. Tan and gray spore-color mutants are used.
The wild type of the spore color of the ...
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...the total number of asci X 100. In order to calculate the map distance, it was necessary to divide the percentage of crossover asci by 2. This has to be performed because only half of the spores in each ascus are result of crossing over. Each student had to count, at least 100 spores, in order to determine if crossing over occurred in a particular perithecium. A data was collected to determine whether various environmental conditions affected the crossing over in Sordaria sp.
In the case of temperatures the cultures were incubated at each determined temperature. For the UV radiation, cells were exposed to UV light for 10 seconds and then grown in 30oC. For the EtBr treatment, 50ul of EtBr was added to the growth medium and cells were incubated at 30oC. In the case of sunlight exposure, cells were exposed to sunlight directly and grown at room temperature
Sordaria fimicola is a species of microscopic fungus that is an Ascomycete and are used to test for genetic variation in the lab setting (Sordaria fimicola: A Fungus used in Genetics, Volk). These organisms are what are called model organisms, or species that has been widely studied usually because it is easy to maintain and breed in a laboratory setting and has particular experimental advantages (Sordaria fimicola, Volk). S. fimicola, because it is in the Ascomycota phylum, have a distinguishing reproductive structure called the ascus, which is surrounded by the perithecium. This cylindrical sac-like structure houses 8 haploid spores; created through meiosis to produce 4 haploid spores and then mitosis to make 8 (Lab Manual, pg. 59-68). Based on the genotype they will vary in order and color. There are 3 different ratios that can arise from the 8 ascospores: 4:4, 2:2:2:2, and 2:4:2 (black/wild type and tan coloration). The 4:4 ratio suggests that no crossing over had occurred because there is no difference in order of the color parents that were mated. The two other ratios suggest genetic recombination, or crossing over, because of the
After 48 hours of incubation the agar plates were viewed. Individual colonies were tested for successful isolation by gram staining and then viewing the stained bacteria under a microscope. Isolation was successful. One colony of each unknown bacteria was transferred to an agar slant for growth. The agar slants were stored at room temperature over the weekend so that they would not grow too much.
The purpose of this experiment is to identify an unknown insert DNA by using plasmid DNA as a vector to duplicate the unknown insert DNA. The bacteria will then be transformed by having it take in the plasmid DNA, which will allow us to identify our unknown insert as either the cat gene or the kan gene.
In order to figure out the genes responsible, there are several other factors that must be determined. These factors include the number of genes involved, if each gene is x-linked or autosomal, if the mutant or wild-type allele for each is dominant, and if genes are linked or on different chromosomes. Proposed crosses include reciprocal crosses between the pure-breeding mutants of strains A and B with the wild-type will help determine if the genes or sex-linked or autosomal, in addition to which alleles are dominant (8). Another proposed cross includes complementation crosses between pure-breading mutants from strains A and B to determine if one or two genes are involved (8). Furthermore, testcrosses between F1 progeny and pure-breeding recessive mutants from strains A and B, which will help determine if genes are linked on the chromosome or if they assort independently (8). These proposed crosses are shown in the attached
Therefore colonies containing the non-recombinant pUC19 plasmid have a functional lacz’ gene appear blue on the agar and colonies containing recombinant pUC19 would have a non-functional lacz’ gene due to insertional inactivation and appear white on the growing medium.
The gels were run at 90-100 volts for 1-1.5 hours. Upon completion of the experiment, we were able to examine the DNA. First, the electrophorese. revealed that three of the fourteen samples were homozygous while the other eleven were
In wild type culture of C-ferns, it is expected that there will be a high concentration of antheridiogen since the hermaphrodites are producing antheridiogen. The greater the population density of C-ferns, the higher the concentration of antheridiogen; hence a high percentage of male gametophytes in the wild type cultures.
Examining the Crosses Between Drosophila Fruit Flies Introduction The major topic of this experiment was to examine two different crosses between Drosophila fruit flies and to determine how many flies of each phenotype were produced. Phenotype refers to an individual’s appearance, where as genotype refers to an individual’s genes. The basic law of genetics that was examined in this lab was formulated by a man often times called the “father of genetics,” Gregor Mendel. He determined that individuals have two alternate forms of a gene, referred to as two alleles.
The second morphological stage of G. lamblia is the cyst form. The cyst is generally egg-shaped and measures eight to fourteen micrometers in length. The width of the cyst is between seven and ten micrometers. When in this form, the original organelle is duplicated. Instead of just having the two nuclei, the microbe now exhibits four nuclei, four median ...
The purpose of this experiment is to conduct genetics studies using drosophila fly as the test organism. Scientists can study the basic biology that is shared by all organisms using a model organism, such as drosophila fly1. Drosophila fly, or more commonly known as fruit fly, has several qualities that makes it well suited for experimental genetics cross. First, fruit flies are low maintenance organisms. They are small in size (few millimeters long), so they occupy a small space and a lot of them can fit in one vial at the same time. They only require a media to feed on. In this lab, instant media was used, which is efficient as it only requires the addition of water to be used. This media contains ingredients that the fruit fly can feed one,
We began this experiment by obtaining four separate vials that contained the four fly genotypes that I mentioned above. We then took the vials of the respective crosses, gently tapped them on the desk to knock the flies to the bottom of the vials, took the stoppers out of the vials and put the open ends together. We had to tap the vials on the desk again to get all of the flies into one vial. We had to perform these procedures for both Cross A and B. After combining the flies into the proper vials, we labeled and turned in to our TA and allowed them to mate for a week.
Plants and Fungi are similar because they lack mobility, both have cell walls, and they both are eukaryotes and multicellular.
This lab report dealt with the analyzation and transmission of genetic traits in monohybrid and dihybrid crosses using Caenorhabditis. Mutations will be either dominant or recessive or X-linked or autosomal. Where using a sterile pick you will pick certain worms and place them in a new petri dish for them to reproduce and observe new progenies, mutations and different crosses.
B. C. LAMB, Related and unrelated changes in conversion and recombination frequencies with temparature in Sordaria (1968)
Spores all the time haploid and unicellular and are generated by meiosis in the sporangium of a diploid sporophyte. Under convenient conditions the spore can use mitotic division to promote into a new organism, which produce a multicellular gametophyte, which eventually goes on to produce gametes. Zygote been formed from Two gametes, which develops into a new sporophyte. This cycle is known as alternation of generations.