Biology: The Dynamic Science (MindTap Course List)
4th Edition
ISBN: 9781305389892
Author: Peter J. Russell, Paul E. Hertz, Beverly McMillan
Publisher: Cengage Learning
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Chapter 11, Problem 12TYK
Discuss Concepts One of the human chromosome pairs carries a gene that influences eye color. In an individual human, one chromosome of this pair has an allele of this gene that contributes to the formation of blue eyes. The other chromosome of the pair has an allele that contributes to brown eye color (other genes also influence eye color in humans). After meiosis in the cells of this individual, what fraction of the nuclei will carry the allele that contributes to blue eyes? To brown eyes?
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Even though the processes are very similar, mitosis and meiosis are two very distinct processes. What is the difference between meiosis and mitosis?
a.
Mitosis results in two identical sister cells genetically identical to the original parent cell, while meiosis also starts with diploid but results in haploid cells.
b.
Mitosis only occurs in plants and single cell organisms, while meiosis only occurs in animals.
c.
Mitosis starts with diploid but results in haploid cells, while meiosis results in two identical sister cells genetically identical to the original parent cell.
In some genetically engineered corn plants, a Bt gene was inserted into a chromosome. The Bt gene specifies a protein called Bt that is lethal to certain flying insect pests that eat the corn plants. If the corn plant is heterozygous for the Bt gene (one homolog has the introduced Bt gene and the other does not), what proportion of the sperm would carry the Bt gene? Is the presence of the Bt gene (a mutation) dominant or recessive to its absence (the wild type)?
A) all pollen; dominant
B) 1/2; dominant
C) 1/3; recessive
D) 1/4; dominant
E) 1/8; recessive
(Explain your answer)
Consider a hypothetical DIPLOID organism with ONE PAIR of homologous chromosomes. How many DNA molecules are there per nucleus in a somatic cell in G1?
4
8
2
1
Picture 1 shows Bob’s chromosome #18 pair. Picture 2 shows Sue’s chromosome #18 pair. Bob and Sue have a stillborn son with three copies of chromosome #18 that look like picture 3. In which parent did the chromosome separation problem occur?
Bob
Sue
Both parents
You need additional information to determine which parent.
Starting with a population of genetically identical mice, you discover two new independent mutant strains in which all of the animals have epileptic seizures. In both strains, you know that the epileptic seizures are due to a single DNA mutation. You cross a mutant mouse from one strain to a mutant mouse from the second strain and find that none of their many offspring undergo spontaneous seizures. From…
Chapter 11 Solutions
Biology: The Dynamic Science (MindTap Course List)
Ch. 11.1 - How does the outcome to meiosis differ from that...Ch. 11.1 - Prob. 2SBCh. 11.1 - Prob. 3SBCh. 11.2 - Prob. 1SBCh. 11.2 - Consider an animal with six pairs of chromosomes;...Ch. 11.3 - Prob. 1SBCh. 11 - The chromosome constitution number of this...Ch. 11 - Which of the following is not associated with...Ch. 11 - Chiasmata: a. form during metaphase II of meiosis....Ch. 11 - If 2n is four, the number of possible combinations...
Ch. 11 - Prob. 5TYKCh. 11 - The DNA content in a diploid cell in G2 is X. If...Ch. 11 - Metaphase in mitosis is similar to what stage in...Ch. 11 - In the human sperm: a. there must be one...Ch. 11 - In plants, the adult diploid individuals are...Ch. 11 - Prob. 10TYKCh. 11 - Discuss Concepts You have a technique that allows...Ch. 11 - Discuss Concepts One of the human chromosome pairs...Ch. 11 - Prob. 13TYKCh. 11 - Prob. 14TYKCh. 11 - Prob. 15TYKCh. 11 - Prob. 1ITDCh. 11 - Prob. 2ITD
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- Consult Figure 1, which shows a human karyotype with chromosomes arranged in order of decreasing size. Would you expect this cell to have any genes characterized as hemizygous? If so, what is an example of a hemizygous gene? On which chromosome would it be located?arrow_forwardSCIENTIFIC INQUIRY The diagram in question 6 represents just a few of the chromosomes of a meiotic cell in a certain person. Assume that the freckles gene is located at the locus marked F, and the hair-color gene is located at the locus marked H, both on the long chromosome. The individual from whom this cell was taken has inherited different alleles for each gene (“freckles” and “black hair” from one parent, and “no freckles” and “blond hair” from the other). Predict allele combinations in the gametes resulting from this meiotic event. (It will help if you draw out the rest of meiosis and label the alleles by name.) List other possible combinations of these alleles in this individual’s gametes. Question is also in the picture.arrow_forwardWhat is the key difference between daughter cells resulting from mitosis and meiosis? In humans, the 4 daughter cells of meiosis contain how many chromosomes? A parent cell has 10 chromosomes. If one daughter cells after mitosis has 9 single chromosomes and the other has 9 single chromosomes and 1 double chromosome, when did the error occur?arrow_forward
- consider the metaphase (mitosis) chromosome spread of the following related animal species. The first meiotic division in the hybrid animal shows a mixture of paired and single chromosomes. Why do you suppose this occurs? Can you suggest a possible relationship between the mixed chromosomes and the observed sterility of the hybrid?arrow_forwardDuring meiosis, when crossing-over occurs between two homologous chromosomes, it does not happen at a single point, but rather two points with a stretch of DNA in between. What are the two junction points called?What is the region between the two points called and what is different about this region compared to how double-stranded DNA usually is?If the region described in b.) is located within a gene and the two homologues have different alleles of this gene, what might happen that is a direct violation of Mendel’s first law? (Describe the process with 2-3 sentences of detail.)arrow_forwardA company that offers PGD terms an embryo “normal and healthy” if it has 46 chromosomes. Why is this statement misleading? , Two famous male actors had twins using a surrogate mother who carried two embryos that hadbeen fertilized in vitro, one with one man’s sperm and the other with the other man’s sperm. In terms of genetics, how closely are the babies, a boy and a girl, related to each other if they have different fathers?arrow_forward
- What is the fundamental difference between mitosis and meiosis? A. DNA is replicated twice in meiosis, but only once in mitosis. B. The number of DNA molecules per cell nucleus is cut in half in meiosis but remains constant in mitosis. C. The number of chromosomes doubles in meiosis, whereas it stays the same in mitosis. D. Mitosis involves two cell divisions, whereas meiosis only involves one.arrow_forwardDiscuss and explain how a child inherits one copy of each gene from each parent. What processes ensure that each cell in your body has a complete set of chromosomes with all the genes?arrow_forwardVISUALIZE Sketch a series of diagrams showing each of the following, making sure to end each series with haploid cells: (a)How a pair of alleles for a single locus segregate in meiosis (b)How the alleles of two unlinked loci assort independently in meiosis (c)How the alleles of two linked loci undergo genetic recombinationarrow_forward
- Identify two ways meiosis contributes to genetic recombination? Why is it necessary to reduce the number of chromosomes in gametes? Blue whales have 44 chromosomes in every cell. Determine how many chromosomes you would expect to find in the following: Cachalot whale Egg cell Daughter cell from mitosis Daughter cell from mitosis IIarrow_forwardConsider a cell with 2 pairs of homologous chromosomes where Chromosome 1 with genes VWXYZ is the homolog of Chromosome 2 with genes vwxyz while Chromosome 3 with genes PQRST is the homolog of Chromosome 4 with genes parst. If a reciprocal translocation occurred between Chromosome 1 YZ genes and Chromosome 3 ST genes, give the following gamete types produced after meiosis: (Answer in Arabic numbers only) 1. Gamete/s with non-recombinant chromosomes 2. Gamete/s with 1 recombinant chromosome 3. Gamete/s with 2 recombinant chromosomes 4. Gamete/s with gene duplications 5. Gamete/s with gene deletions 6. Gamete/s with 2 normal chromosome sequences 7. Gamete/s with 1 normal chromosome sequence 8. Gamete/s with balanced translocation 9. Gametes/ with all dominant genes 10. Gamete/s with all recessive genes 11. Gamete/s with 10 different genes 12. Gamete/s with TSXWV genes 13. Gamete/s with vwxyz genes 14. Gamete/s with pqrst genes 15.Gamete/s with PORYZarrow_forwardWe say that genes that are close together on the same chromosome are linked. What does that mean? Imagine that in a diploid nucleus, one chromosome has the allele R and right next to it on the same chromosome is the allele T for a different gene. Are these linked? Imagine that r is right next to t on the homologous chromosome. If this cell never undergoes meiosis, does this matter at all? If it does undergo meiosis, what are the two genotypes that the gametes are most likely to have? Look at Figure for help if you need it.arrow_forward
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