Preview

Crosses of Sordara

Better Essays
Open Document
Open Document
1224 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Crosses of Sordara
Biology 260: gENETICS | CROSSES OF SORDARIA | Sordaria of Tan and Grey Allele | |

Abstract:
To understand the details of genetic behavior, Sordaria fimicola is used in this study by observing the asci produced from monohybrid and dihybrid crosses with observance to recombination. This experiment performed extended over a three week period. The strains that were used from S. fimicola were wild type producing black, and mutants producing grey and tan strains. There are seven possible phenotypes as a result from second division segregations through the dihybrid crosses. Map units were found through results of the monohybrid cross. Expected map unit results are 33 mu for grey and 28 mu for tan. However, our results differ from that expected, 24.7 mu for the grey and 25.1 for tan. The differentiation may be due to certain factors like temperature, time, and maturation of the perithecial.
Introduction:
S. fimicola is a fungus that produces asci contained in a perithecium, and individual ascus’ have ordered ascospores that are used in studies of genetics because through ascospores is the way S. fimicola reproduces. S. fimicola has a short life span and is good in studies for genetics because S. fimicola stays in a haploid state and also tetrad analysis allows for a direct observation of crossing-over. This study is extremely helpful in understanding crossing over because it’s easy to see that the genetic material that were previously on separate homologs have combined, and through laboratory experiment there’s a visual interpretation of genetic variation (Glase, 2005). S. fimicola is an excellent candidate for studying recombination and genetics and has been used in many studies.
Studies of this fungus, for educational purposes and the establishing was first accomplished by obtaining spore colored mutants of S. fimicola through ultraviolet irradiation in 1956. Further, the mutants of S. fimicola were crossed with the wild strain resulting in visible



Cited: Cassel, P and T.R. Mertens (1968) “A laboratory Exercise on the Genetics of Ascospore Color in Sordaria fimicola”. The American Biology Teacher 30:367-372 Glase, J.C. (2005) “A Study of Gene Linkage and Mapping Using Tetrad Analysis in the Fungus Sordaria fimicola” in Tested studies for laboratory teaching. 16:1-24 Olive, L.S. (1974) “Sordaria” R.C. King ed. Handbook of Genetics, Plenum Press, NYC. pp 553-556

You May Also Find These Documents Helpful

  • Powerful Essays

    Types of Fungi

    • 1486 Words
    • 6 Pages

    Do an Internet search for a microscopic image of young hyphae of Morchella (Ascomycota) or some other filamentous fungus. Answer the following questions:…

    • 1486 Words
    • 6 Pages
    Powerful Essays
  • Better Essays

    Nt1310 Unit 1 Exercise 1

    • 1475 Words
    • 6 Pages

    De la Parte, E. M. & Dita, M. (2014) Basic Aspects of Molecular Biology and DNA Extraction [Lecture slides]. Retrieved from http://www.fao.org/fileadmin/templates/agphome/documents/Pests_Pesticides/caribbeantr4/10MolecularBiology.pdf…

    • 1475 Words
    • 6 Pages
    Better Essays
  • Satisfactory Essays

    Hsc2 Unit 1 Assignment

    • 402 Words
    • 2 Pages

    i) The enzyme that would be used to cut the vector would be SalI along with adding the CIP. The main reason that you would cut with the particular enzyme Sal I is because the beginning of the vector sequence there isn’t a stop codon, so but cutting it with Sal I than both the vector and the protein will be compatible. There however is going to be a function of the CIP. CIP is a very important aspect of the whole process because once the vector is opened; the CIP is going to…

    • 402 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Ambrosia Beetle Hypothesis

    • 1318 Words
    • 6 Pages

    DNA extraction of the fungi. The sequence will be compared to the sequences obtained by…

    • 1318 Words
    • 6 Pages
    Good Essays
  • Better Essays

    Lab Report Part II

    • 1247 Words
    • 4 Pages

    Background Information: The process begins with preparing a sample. Successful identification starts with using a sample that is considered to be good. The first step is to pick up a single colony and drop it into a microcentrifuge tube. A buffer is used to dissolve the cell wall in order to extract bacterial DNA. This step may take several hours. The proteolytic enzymes need to go before proceeding. Heating the sample in a water bath at 100 degrees Celsius denatures them. Next, cellular debris is spun down in the centrifuge and appears as a pellet at the bottom. The DNA is contained in the liquid, which is then transferred to the tube. To continue the process, PCR amplification is conducted. One must add PCR Master Mix solution to the sample DNA to prepare the polymerase chain reaction. The mix contains water, a buffer to keep the correct pH for the reaction; large quantities of the four nucleotides; large quantities of oligonucleotide DNA primers; and a heat-stable DNA polymerase. At the same time, one will prepare negative and positive control reactions. The positive contains positive control DNA while the negative contains sterile deionized water. Both contain the PCR solution. Once reaction tubes have been loaded onto the PCR machine, DNA replication starts. By doing this, one can know temperature, time remaining, cycle number, melt, anneal, and extend. The first step, melt, is to separate the two DNA chains in the double helix by heating the vial containing the PCR reaction mixture to 95 degrees Celsius for 30 seconds. The vial is cooled at 60 degrees Celsius. The final step, extend, is to allow the DNA polymerase to extend the copy DNA strand by raising the temperature to 70 degrees Celsius for 45 seconds. Separation of the strands, annealing the primer to the template, and the synthesis of new strands…

    • 1247 Words
    • 4 Pages
    Better Essays
  • Better Essays

    Sordaria Lab Report

    • 932 Words
    • 4 Pages

    To achieve genetic experiments with haploid organisms, genetic strains of different genotypes must be crossed from one another. Following fertilization and meiosis, the meiotic products can be analyzed as the ascomycete fungus, Sordaria fimicola. Sordaria can be used as a model to study meiotic segregation. The trait followed was the ascospore color. Ascospore color is a single gene trait therefore it is easily observed under a light microspore. Which allele is dominant is very tough to say, because dominant and recessive does not apply in this case. Sexual spores are confined in a saclike form called asci (singular - ascus). Inside the asci, karyogamy occurs and combines the two parental genomes, and then meiosis forms genetically diverse ascospores. Eight ascospores can be found lined up in a row in the asci; they form a single zygote, which is diploid.…

    • 932 Words
    • 4 Pages
    Better Essays
  • Powerful Essays

    Sordaria Lab Report

    • 1466 Words
    • 6 Pages

    Using a compound microscope, locate the asci using the 100x magnification. Once located, observe under 400x magnification. Look for ascus sacs that contain more than one spore color. These were formed by the fusion of the two strains.…

    • 1466 Words
    • 6 Pages
    Powerful Essays
  • Satisfactory Essays

    Genetics Lab Report

    • 581 Words
    • 3 Pages

    To analyze if diploid yeast strain heterozygous for ARG8 ADE2 HIS3/arg8 ade2 his3 on chromosome XV and TRP1/trp1 on chromosome IV irradiated with UV light underwent mitotic recombination to form homozygous recessive ade2/ade2 mutants. The ade2/ade2 mutant are selected then plated on different media to observe if the homozygous recessive mutants were due to mitotic recombination.…

    • 581 Words
    • 3 Pages
    Satisfactory Essays
  • Better Essays

    Sordoria Lab

    • 1569 Words
    • 7 Pages

    Species of the genus Sordaria share a number of characteristics that are advantageous for genetic studies. They all have a short life cycle, usually 7-12 days, and are easy to grow on nutrient agar in dish cultures. All kinds of mutants are easily induced and readily obtainable with particular ascospore color mutants. These visual mutants aid in tetrad analysis, especially in analysis of intragenic recombination. ( Campbell 72)…

    • 1569 Words
    • 7 Pages
    Better Essays
  • Good Essays

    Sordaria

    • 516 Words
    • 3 Pages

    closely related to Neurospora and Podospora, is a member of the numerous class Pyrenomycetes or flask-fungi. The natural habitat of the three species of Sordaria that have been the principal subjects in genetic studies is the dung of herbivorous animals. The species S. fimicola is common and worldwide in distribution. The species of Sordaria are similar morphologically, producing black perithecia containing asci with eight dark ascospores in a linear arrangement. These species share a number of characteristics that are advantageous for genetic studies.…

    • 516 Words
    • 3 Pages
    Good Essays
  • Better Essays

    Sordaria Research Paper

    • 1698 Words
    • 7 Pages

    Sordaria is an Ascomycota that uses a special spore formation process in reproduction. Ascomycota’s use both meiosis and mitosis division to produce eight spores (asci). These asci are held in a sac called a perithecium or ascus, a fruiting body that rupture and release the ascospores when they’ve reached maturity (Cyr, R. 2002). These spores are easily viewed under a microscope and have mutant strain colors with different patterns that serve as proof of crossover events. Wild-type (black spores) and non-black spores (tan) we used to detect crossing over. The asci can be arranged in 4:4: meaning 4 black spores and 4 tan spores, which indicate no crossing over occurred. Asci can also be arranged with alternating tan and black in groups of two. 2:4:2 arrangements also occur meaning 2 black spores, 4 tan then another 2 black spores. 2:2:2:2 and 2:4:2 are both an indication that crossover has taken place. When spores of the organism were crossed with strains from the same slope and from different slopes, it was found that the crossover frequencies were greater on the South Facing slope rather than on the North Facing Slope (Hass, C. and Ward, A. 2010). These findings led to a correlation between harsher environments and high cross over frequencies and also many questions.…

    • 1698 Words
    • 7 Pages
    Better Essays
  • Better Essays

    Gold Fish Lab Report

    • 1120 Words
    • 5 Pages

    Cited: White, M. E. and F. M. Campo. 2008. Investigations in Biology, 4th Ed. The McGraw-Hill Co. Inc., New York, NY, USA.…

    • 1120 Words
    • 5 Pages
    Better Essays
  • Powerful Essays

    Igenetics Study Guide

    • 4404 Words
    • 18 Pages

    Answer: Genetic maps can be used in the process of localizing genes and studying the distribution of genes on chromosomes and in the genome.…

    • 4404 Words
    • 18 Pages
    Powerful Essays
  • Better Essays

    Cited: 1) Campbell, N. A. and J. B. Reece. 2002. Biology. 6th ed. Prentice Hall.…

    • 1062 Words
    • 4 Pages
    Better Essays
  • Satisfactory Essays

    Clinical Observations Indicative for Fusariosis:Some clinical observations may give a first hint to Fusarium being the etiological agent causing an infection. Morphological characteristics of cultures, has long been used to identify fungal isolates,this is still the standard for identification Fusarium grow rapidly on Sabouraud dextrose agar at 25C and produce woolly to cottony, flat, spreading colonies, and may display a variety of colors from the surface (creamy, white, tan, salmon, cinnamon, yellow, red, violet, pink or purple) or the reverse (colorless, tan, red, dark purple or brown). Fusarium will grow on all fungal media not containing cyclohexamide. The diagnosis of Fusarium is based on macroscopic and microscopic features including…

    • 123 Words
    • 1 Page
    Satisfactory Essays

Related Topics