Essentials of Genetics (9th Edition) - Standalone book
9th Edition
ISBN: 9780134047799
Author: William S. Klug, Michael R. Cummings, Charlotte A. Spencer, Michael A. Palladino
Publisher: PEARSON
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Chapter 2, Problem 18PDQ
Summary Introduction
To review:
The probability that in anorganism (haploid number of chromosomes or n is10), a spermformed will contain all 10 chromosomes, withcentromeres derived from maternal homologs.
Introduction:
Meiosis is the process of cell division, in which a single cell dividesinto two phases and it leadsto the production of four daughter cells. The daughter cells contain half the amount of parental cell’s genetic information. Meiosis occurs during the formation of gametes (a sperm and an egg).
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What is the probability that, in an organism with a haploid number of 10, a sperm will be formed that contains all 10 chromosomes whose centromeres were derived from maternal homologs?
During metaphase I of meiosis, tetrads align along the metaphase plate independently of each other. Therefore, there is a random “shuffle” of maternal and paternal chromosomes in the resulting gametes.The following diagram demonstrates how this works in a diploid cell with four chromosomes (2n=4) . Because there are two pairs of chromosomes and each pair can align in one of two ways during metaphase I, the number of possible variations in the gametes produced is 22 or 4.For an organism that is , there are three pairs of chromosomes, so the number of possible variations in the gametes produced due to independent assortment in metaphase I is 23 or 8.
In an organism with a haploid number of 7, how many possible combinations of maternal and paternal chromosomes can occur in its gametes?
a. 72=49
b. 27=128
c.17=1
d. 214=16 384
Though an individual with abberations such as Robertsonian translocation may be phenotypically normal, they can generate gametes through meiosis that have atypical organizations of chromosomes, resulting in recurrent fetal abnormalities or miscarriages. Why, despite these Robertsonian translocations, are affected cells still able to generate typical gametes through meiosis?
Chapter 2 Solutions
Essentials of Genetics (9th Edition) - Standalone book
Ch. 2 - CASE STUDY | Timing is everything A man in his...Ch. 2 - CASE STUDY | Timing is everything A man in his...Ch. 2 - CASE STUDY | Timing is everything A man in his...Ch. 2 -
HOW DO WE KNOW?
1. In this chapter, we focused...Ch. 2 -
2. Review the Chapter Concepts list on page 12....Ch. 2 - What role do the following cellular components...Ch. 2 -
4. Discuss the concepts of homologous...Ch. 2 - If two chromosomes of a species are the same...Ch. 2 - Describe the events that characterize each stage...Ch. 2 - How are chromosomes named on the basis of their...
Ch. 2 - Prob. 8PDQCh. 2 -
9. Describe the phases of the cell cycle and the...Ch. 2 - Define and discuss these terms: (a) synapsis, (b)...Ch. 2 - Prob. 11PDQCh. 2 - Prob. 12PDQCh. 2 - Contrast spermatogenesis and oogenesis. What is...Ch. 2 -
14. Explain why meiosis leads to significant...Ch. 2 -
15. A diploid cell contains three pairs of...Ch. 2 - Prob. 16PDQCh. 2 -
17. During oogenesis in an animal species with a...Ch. 2 - Prob. 18PDQCh. 2 -
19. During the first meiotic prophase, (a) when...Ch. 2 -
20. Describe the role of meiosis in the life...Ch. 2 - Prob. 21PDQCh. 2 - Prob. 22PDQCh. 2 - Prob. 23PDQCh. 2 -
24. If one follows 50 primary oocytes in an...Ch. 2 -
25. The nuclear DNA content of a single sperm...Ch. 2 - For Problems 26–31, consider a diploid cell that...Ch. 2 - For Problems 26–31, consider a diploid cell that...Ch. 2 - For Problems 26–31, consider a diploid cell that...Ch. 2 -
For Problems 26–31, consider a diploid cell that...Ch. 2 - For Problems 26–31, consider a diploid cell that...Ch. 2 - For Problems 26–31, consider a diploid cell that...
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- Assume that a meiotic-nondisjunction event causes trisomy 8 in a newborn. If two of the three copies of chromosome 8 are absolutely identical, at what point during meiosis did the nondisjunction event take place?arrow_forwardHuman sex chromosomes are XX for females and XY for males. a. With respect to an X-linked gene, how many different types of gametes can a male produce? b. If a female is homozygous for an X-linked allele, how many different types of gametes can she produce with respect to this allele? c. If a female is heterozygous for an X-linked allele, how many different types of gametes can she produce with respect to this allele?arrow_forwardConsider a diploid cell that contains 7 pairs of chromosomes. Each pair includes a maternal and a paternal member (for example: AP pair) or AP B ^ n * B ^ p (two pairs). How many different combinations of chromatids are possible during the early phases of anaphase in meiosis II?arrow_forward
- During metaphase I of meiosis, tetrads align along the metaphase plate independently of each other. Therefore, there is a random “shuffle” of maternal and paternal chromosomes in the resulting gametes.The following diagram demonstrates how this works in a diploid cell with four chromosomes . Because there are two pairs of chromosomes and each pair can align in one of two ways during metaphase I, the number of possible variations in the gametes produced is , or .For an organism that is , there are three pairs of chromosomes, so the number of possible variations in the gametes produced due to independent assortment in metaphase I is , or . In an organism with a haploid number of , how many possible combinations of maternal and paternal chromosomes can occur in its gametes? Select one: a. 72=49 b. 27=128 c.17=1 d. 214=16 384arrow_forwardAn individual heterozygous for a reciprocal translocation possesses the following chromosomes: A B • C D E F G A B • C D V W X R S • T U E F G R S • T U V W X Q. Draw the pairing arrangement of these chromosomes in prophase I of meiosis.arrow_forwardA cell has four pairs of chromosomes. Assuming that crossing over does not occur, what is the probability that a gamete will contain all of the paternal chromosomes? If n equals the number of chromosomes in a set, which of the following expressions can be used to calculate the probability that a gamete will receive all of the paternal chromosomes: (1/2)n, (1/2)n–1, or n1/2?arrow_forward
- Suppose that meiosis occurs in the transient diploid stageof the cycle of a haploid organism of chromosome number n. What is the probability that an individual haploidcell resulting from the meiotic division will have a complete parental set of centromeres (that is, a set all fromone parent or all from the other parent)?arrow_forwardA male Drosophila melanogaster has the genotype A/a; B/b; C/c; XD/Y (all genes are on separate chromosomes). How many different sperm genotypes can it produce through meiosis of one single pre-gametic (2n) cell? (remember, there is no crossing over in male Drosophila) Explain.arrow_forwardA diploid cell has 15 picograms of DNA in G₁ phase. If this cell is a germ line cell that undergoes meiosis, how much DNA will each daughter cell contain at the end of meiosis I? How much DNA will each daughter cell contain at the end of meiosis II? MI = 30 pg: MII = 15 pg O MI = 15 pg; MII = 15 pg MI = 7.5 pg; MII = 15 pg O MI = 15 pg: MII = 7.5 pgarrow_forward
- Meiosis is characterized by the pairing of homologouschromosomes during prophase I. In many species, an elaboratestructure called the synaptonemal complex forms betweenhomologues. During this pairing, homologues may exchangechromosomal material at sites called chiasmata. In meiosis I, thehomologues separate from each other, reducing the chromosomenumber to the haploid state (thus the reductive division). It isfollowed by a second division without replication, during whichsister chromatids become separated. The result of meiosis I and IIis four haploid cells. If sister chromatids separated at the first division, would meiosis still work?arrow_forwardAssume that you were examining a first polar body and noted that it had one copy (dyad) of each chromosome except chromosome 21. Chromosome 21 was completely absent. What would you expect to be the chromosome 21 complement (only with respect to chromosome 21) in the secondary oocyte? What consequences are likely in the resulting zygote if the secondary oocyte was fertilized?arrow_forwardKuliev and Verlinsky (2004) state that there was a relatively high number of separation errors at meiosis I. In these cases the centromere underwent a premature division, occurring at meiosis I rather than meiosis II. Regarding chromosome 21, what would you expect to be the chromosome 21 complement in the secondary oocyte in which you saw a single chromatid (monad) for chromosome 21 in the first polar body? If this secondary oocyte was involved in fertilization, what would be the expected consequences?arrow_forward
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