Preview

Chapter 15: The Chromosomal Basis Of Inheritance

Good Essays
Open Document
Open Document
4682 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Chapter 15: The Chromosomal Basis Of Inheritance
Biology, 7e (Campbell)
Chapter 15: The Chromosomal Basis of Inheritance

Chapter Questions

1) Chromosomes and genes share all of the following characteristics except that
A) they are both present in pairs in all diploid cells.
B) they both undergo segregation during meiosis.
C) their copy numbers in the cell decrease after meiosis, and increase during fertilization.
D) they are both copied during the S phase of the cell cycle.
E) they both pair up with their homologues during prophase of mitosis.
Answer: E
Topic: Concept 15.1
Skill: Knowledge

2) The improvement of microscopy techniques in the late 1800s set the stage for the emergence of modern genetics because
A) it revealed new and unanticipated features of
…show more content…
Wild type (heterozygous for normal wings and red eyes) × recessive homozygote with vestigial wings and purple eyes

74) What pattern of inheritance would lead a geneticist to suspect that an inherited disorder of cell metabolism is due to a defective mitochondrial gene?
Answer: The disorder would always be inherited from the mother.

75) Women born with an extra X chromosome (XXX) are healthy and phenotypically indistinguishable from normal XX women. What is a likely explanation for this finding? How could you test this explanation?
Answer: The inactivation of two X chromosomes in XXX women would leave them with one genetically active X, as in women with the normal number of chromosomes. Microscopy should reveal two Barr bodies in XXX women.

76) Determine the sequence of genes along a chromosome based on the following recombination frequencies: A-B, 8 map units; A-C, 28 map units; A-D, 25 map units; B-C, 20 map units; B-D, 33 map units.
Answer: D-A-B-C

77) Assume that genes A and B are linked and are 50 map units apart. An animal heterozygous at both loci is crossed with one that is homozygous recessive at both loci. What percentage of the offspring will show phenotypes resulting from crossovers? If you did not know that genes A and B were linked, how would you interpret the results of this

You May Also Find These Documents Helpful

  • Good Essays

    Kumabjara of Namjbar

    • 667 Words
    • 3 Pages

    c. Write out the genotypes of the F1 dragons that will be used to breed and give rise to the F2…

    • 667 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    g. The nucleic acid which picks up amino acids in the cytoplasm and then takes them to…

    • 306 Words
    • 3 Pages
    Satisfactory Essays
  • Better Essays

    Nt1310 Lab 6.2

    • 1483 Words
    • 6 Pages

    T 4. In a cross between two homozygous dominant individuals, 25% of the offspring may have the recessive phenotype.…

    • 1483 Words
    • 6 Pages
    Better Essays
  • Good Essays

    Bio 156 lab 7 genetics

    • 916 Words
    • 3 Pages

    b. What is the phenotype for the trait? Is this the dominant or recessive allele for the trait? (2 points)…

    • 916 Words
    • 3 Pages
    Good Essays
  • Good Essays

    P1: Explain how sperm and ova are formed by producing an annotated diagram of meiosis and discussing what happens in ogenesis and spermatogenesis…

    • 639 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Mastering Biology

    • 2505 Words
    • 11 Pages

    - two cells, each with the same amount of genetic material and the same genetic information…

    • 2505 Words
    • 11 Pages
    Good Essays
  • Satisfactory Essays

    Biology Chromosome

    • 859 Words
    • 4 Pages

    c. This syndrome can only be held “responsible” to both the parents chromosome contributions. The mother could achieve nondisjunction anywhere throughout meiosis to achieve the double XX chromosome in one of the final egg gametes. The father if had nondisjunction in the final division could end up with two XX chromosomes in the final sperm gamete at the end of meiosis.…

    • 859 Words
    • 4 Pages
    Satisfactory Essays
  • Satisfactory Essays

    Yellow Wallpaper

    • 932 Words
    • 4 Pages

    Sexual reproduction and the close association between homologous chromosomes that occurs during meiosis probably evolved as a mechanism to repair __________ damage.…

    • 932 Words
    • 4 Pages
    Satisfactory Essays
  • Good Essays

    Give an example of a dominant and recessive genetic disorder. People with light eyes tend to carry recessive alleles of the major genes; people with dark eyes tend to carry dominant alleles.…

    • 369 Words
    • 1 Page
    Good Essays
  • Good Essays

    X Rated Summary

    • 1290 Words
    • 6 Pages

    To add to the credibility of the article, she describes studies executed by several other scientists reaching the same conclusions. Methods used to conduct the experiments were observation and testing. The facts were presented in a logical manner, but were obviously tailored to an audience that already has insight into genetics. Also contributing to the credibility of the author 's research is the extensive list of references following the conclusion of the article. While X rated was a fascinating read, the reader gains more specific facts in Intelligence and the X chromosome and thus has a greater understanding of the…

    • 1290 Words
    • 6 Pages
    Good Essays
  • Good Essays

    Genetic information is complex and overwhelming and there are many resources available via the internet containing detailed facts on the subject. For this assignment, I will summarize information that is available from various genetic websites and who might find these types of sites useful. I will also select two abnormalities of sex chromosomes and two gene-linked abnormalities from Chapter 2 of our text entitled Child Development (Santrock, 2014) and use the information from the websites to provide a brief report on each abnormality.…

    • 792 Words
    • 4 Pages
    Good Essays
  • Satisfactory Essays

    hardy

    • 798 Words
    • 4 Pages

    5) Tay-Sachs disease is inherited as a Mendelian recessive and occurs in Ashkenazic Jews at a frequency of 1 per 3,600 births. Estimate the percentage of this population that are heterozygote carriers of the Tay-Sachs allele.…

    • 798 Words
    • 4 Pages
    Satisfactory Essays
  • Good Essays

    Karyotype: Sex Chromosomes

    • 1225 Words
    • 5 Pages

    1. The attached sheet was used to complete one out of two normal karyotypes ( Chromosome Pic #2 and #3) and another out of the four sets of abnormal karyotypes ( Set A, B, C, and D).…

    • 1225 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Mitosis and Meiosis

    • 745 Words
    • 3 Pages

    1. A certain species has three pairs of chromosomes: an acrocentric pair, a metacentric pair, and a telocentric pair. Draw a cell of this species as it would appear in metaphase of mitosis. (BAP 2.18) 2. A cell in G1 of interphase has 12 chromosomes. How many chromosomes and DNA molecules will be found per cell when this original cell progresses to the following stages? (BAP 2.20) a) G2 of interphase b) Metaphase I of meiosis c) Prophase of mitosis d) Anaphase I of meiosis e) Anaphase II of meiosis f) Prophase II of meiosis g) After cytokinesis following mitosis h) After cytokinesis following meiosis II 3. How would the answers to the above question change if the question had asked about centromeres and chromatids rather than chromosomes and DNA molecules? 4. The fruit fly Drosophila melanogaster has four pairs of chromosomes, whereas the house fly Musca domestica has six pairs of chromosomes. Other things being equal, in which species would you expect to see more genetic variation among the progeny of a cross? Explain your answer. (BAP 2.24) Calculate the number of possible chromosome combinations in the two fly species described above, then calculate the number of possible chromosome combinations in crosses unrelated individuals for each species. 5. Female bees are diploid and male bees are haploid. The haploid males produce sperm and can successfully mate with diploid females. Fertilized eggs develop into females and unfertilized eggs develop into males. How do you think the process of sperm production in male bees differs from sperm production in other animals? (BAP 2.29) 6. A mythical beast called the paradoxitaur (see, it’s an imaginary creature that only exists if you don’t believe in it) has cells that contain 14 chromosomes, some cells with 7 chromosomes and some with 28 chromosomes. It seems that it only has 7 linkage groups. Assuming all cells are normal and healthy,…

    • 745 Words
    • 3 Pages
    Good Essays
  • Good Essays

    With all these overwhelming evidences in favor of nuclear inheritance it was but natural for geneticists to believe that nucleus is the only seat where all the genetic potentialities are located…

    • 680 Words
    • 3 Pages
    Good Essays