Y Chromosome Evolution

Improved Essays
Y chromosome is a sex determine chromosome among many species including modern humans. Modern studies in genome suggested that Y chromosome arose from the accumulations of mutations of other chromosomes and have some special genes on it which determine the gender of the carrier; however, some non-mammalian animals carry the Y chromosome even if their genders are not determine by the appearance of the Y chromosome. The Y chromosome works differently on the mammalian and non-mammalian so in this paper when an aspect about Y chromosome is brought up, it well be discussed in both mammalian (use human as example) and non-mammalian (use Drosophila as example) case.
The paper will mainly focus on three point: how Y chromosome originated; the function
…show more content…
2009); the same study also found that in Drosophila pseudoobscura the Y chromosome had a large portion of itself that was not homologous as the X chromosome. All these evidences suggest that the Drosophila Y chromosome has an alternative origin than the mammalian Y …show more content…
The Y chromosome also has several microsatellite sequences on it, what makes these microsatellite sequences special is that these sequences locate on the non-recombining region, meaning that they are likely to be preserved along the time. Therefore, it is possible to use these microsatellite sequences to generate a phylogenetic tree for Y chromosome, and researchers did that in 2002: by using the polymorphism mutations exist in the non-recombining region of Y chromosome, the researchers made a phylogenetic tree for 153 Y chromosome haplogroups, which helps other researchers to further study the Y chromosome evolution (Y Chromosome Consortium 2002). Then in 2003 researchers used the generated phylogenetic tree to construct a map that showed the distribution of different Y chromosome haplogroups around the world (Jobling & Tyler-Smith 2003). In 2013 by studying the human Y chromosome, researchers have found a human Y chromosome that presented the ancestral states for all the polymorphism sites, which meant that it was the ancestor of all the known human Y chromosome (Mendez et al. 2013); this finding suggests that the now known most recent common ancestor of human Y chromosome existed about 338 thousand years

Related Documents

  • Great Essays

    Questions 2: a) 45 chromosomes with one sex chromosome, chromosome Y. There would be a spontaneous miscarriage, as monosomy Y is not viable, resulting in no phenotype. b) 47 chromosomes with an extra chromosome 18 and 2 X sex chromosomes. The resulting phenotype is a female with Edwards Syndrome. c) 45 chromosomes with one less chromosome 21 and a X and Y sex chromosome.…

    • 699 Words
    • 3 Pages
    Great Essays
  • Improved Essays

    The basic principles are simple; the X-sperm contains more DNA than the Y-sperm. Although this difference is small, it is possible to measure DNA content of individual sperm with sufficient accuracy to distinguish between X- and Y-sperm with about 90% accuracy for 50% of the sperm. Therefore, about half of the sperm are discarded as unsexable. The DNA content of sperm is determined using a fluorescing dye, Hoechst 33342 that readily penetrates the sperm cell membrane and binds to the DNA stoichiometrically. Thus, X-sperm ends up with about 4% more dye bound to their DNA than Y-sperm.…

    • 522 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Week 3 Assignment

    • 582 Words
    • 3 Pages

    In a few cases, however, they do. Explain how. Inversions and reciprocal translocations do not usually cause a phenotypic effect because of the person who is possessing these are able to equal the look alike numbers genetic components as a ordinary person. They would be able to possess a regular phenotype. It is also possible that the disengagement of the position of the chromosomes was able to influence the gene that was attempting to be expressed.…

    • 582 Words
    • 3 Pages
    Improved Essays
  • Great Essays

    Fruit Fly Lab Report

    • 1571 Words
    • 7 Pages

    These gene is a vital part of the integrated process of development. In drosophila, it determines the dorsal-ventral axis and also controls the development of the fly’s wings. Without this axis, the determination of where appendages develop can be incomplete or incorrect resulting in wings or feet in the wrong places. Major mutations during development are often lethal. In addition, wing development is extremely important for both survival and reproduction in drosophila.…

    • 1571 Words
    • 7 Pages
    Great Essays
  • Improved Essays

    Fruit Flies Lab Report

    • 894 Words
    • 4 Pages

    The data was able to support the statement above because based on the data, there was only two phenotype and they both have normal wing for the male and the female. Fruit flies does…

    • 894 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    When compared to the mutant female, mutant male Drosophila expressed several unique differences. The mutant males exhibited smaller and darker colored eyes compared…

    • 281 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Morgan had a very keen sense towards teaching. He is also known as being a successful teacher. He began to research sex linkage on the fruit fly, or Drosophila, in 1909. Before his discovery, the world had thought that the chromosomes were fully formed adults already present in the egg or sperm. People did not have the knowledge to test that theory, until Thomas Hunt Morgan began to research the chromosomes of the male fruit fly (Thomas Hunt Morgan, American Biologist, n.d.).…

    • 852 Words
    • 4 Pages
    Improved Essays
  • Decent Essays

    COLUMN 2: Behind Column 2

    • 571 Words
    • 3 Pages

    COLUMN 2: Behind Column 1 What causes this disorder? A chromosomal mutation called translocation. Translocation is when the chromosome breaks and a portion of that chromosome reattaches to another chromosome. This chromosome that is affected by this is the 8 and 14 chromosome pair.…

    • 571 Words
    • 3 Pages
    Decent Essays
  • Great Essays

    In this lab, the purpose was to demonstrate how the Drosophila melanogaster is used in the field of genetics to study the inheritance of traits throughout the F1 and F2 generations. Drosophila melanogaster was introduced into the wild type and other mutant alleles such as white eyed, vestigial, and sepia. The results gathered in the lab would then be compared to actual results, and a Chi-Square test will be used for…

    • 4136 Words
    • 17 Pages
    Great Essays
  • Improved Essays

    Fruit Fly Lab Report

    • 395 Words
    • 2 Pages

    Introduction Fruit fly Drosophila melanogaster that is used as a model to study genetics for more than a hundred years. Thomas Hunt Morgan, in the early 1900’s, used the heritable traits of a common species of fruit fly to develop our understanding of genetics. Morgan was the first to show through experiments that genes were located on chromosomes. He also found that certain fruit fly traits like eye color are found on the same chromosomes that also determine their sex. Fruit flies have several characteristics that make them excellent subjects for genetic studies.…

    • 395 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Creating Food Lab Report

    • 2497 Words
    • 10 Pages

    The marker chromosomes used in the experiment are Cy, Pm, D, Sb. Cy and Pm are located on chromosome 2. D and Sb are located on chromosome 3. 66 out of 263 flies (25%) of the marker DC1 cross was Cy/D. 61 out of 263 flies (23%) are Cy/Sb. 65 out of 263 flies (25%) are Pm/D. 71 out of 263 flies (27%) are Pm/Sb.…

    • 2497 Words
    • 10 Pages
    Improved Essays
  • Improved Essays

    Fruit Fly Lab Report

    • 1262 Words
    • 6 Pages

    If there are two X’s it is a female whereas, if there is one X and a Y, it is a male. The female flies are larger than the males as well as have a pointed abdomen rather than round. A gene is a heredity unit, thus made up of DNA (King & Stansfield, 1985, p.151). Two alleles are inherited from each gene, hence, if homozygous, the alleles are the same, and if heterozygous, the alleles are different (King & Stansfield, 1985, p.14). The mode of inheritance is determined through experimental crosses to identify if the mutation is autosomal or X-linked, and also dominant or recessive.…

    • 1262 Words
    • 6 Pages
    Improved Essays
  • Improved Essays

    Y-STRs are derived from male sex-determining Y-chromosomes. It is much stronger to use autosomal STR because autosomal DNA is randomly exchanged between matched pairs of sperm and egg cells. This is the primary reason why no two people are alike. In addition to this, Y-STRs are much weaker due to them based on the Y-chromosome, which all males obtain from their fathers. Thus, all males in any paternal line have nearly the same…

    • 471 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    This was done through DNA analysis by the Y-chromosome DNA of men and the mitochondrial DNA that we inherit from our mothers. Along the way, they…

    • 737 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Kennedy's Disease

    • 411 Words
    • 2 Pages

    Introduction How do you define Kennedy’s disease? Kennedy’s disease is a rare inherited disease that disturbs the males in the family by progressively weakening and wasting the motor neurons in the muscles (Kennedy's Disease Association, 2015). Kennedy’s disease got its name from the studies by Dr. William R. Kennedy who found patients with the rare disorder back in 1968, which had occurred in the later part of the adult life. Kennedy’s disease starts to appear in males between the ages of 30 to 50 years old.…

    • 411 Words
    • 2 Pages
    Improved Essays

Related Topics