Genetics: Analysis and Principles
6th Edition
ISBN: 9781259616020
Author: Robert J. Brooker Professor Dr.
Publisher: McGraw-Hill Education
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Textbook Question
Chapter 8.4, Problem 3COMQ
A mechanism that may cause a translocation is
a. the joining of reactive ends when two different chromosomes break.
b. crossing over between nonhomologous chromosomes.
c. crossing over between homologous chromosomes.
d. either a or b.
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Chromosome translocations include:
A. Alterations in which the genetic material remains the same but rearranged
B. Alterations in which the total amount of genetics information increases
C. Alterations in which the total amount of genetics information decreases
D. Variations in the chromosome number
Altered chromosome structure can drastically affect an individual organism’s phenotype. However, some types of chromosomal rearrangements are more likely to be harmful than others. Categorize the following types of rearrangements from MOST LIKELY to be harmful to LEAST LIKELY to be harmful.
A. reciprocal translocation, deletion, translocation
B. deletion, translocation, inversion
C. inversion, translocation, reciprocal translocation
D. translocation, inversion, duplication
During crossing over,a. chromatids of homologous chromosomes exchange parts.b. mutations occur with higher than average frequency.c. chromatids of nonhomologous chromosomes exchange parts.d. nondisjunction occurs.
Chapter 8 Solutions
Genetics: Analysis and Principles
Ch. 8.1 - 1. A chromosome that is metacentric has its...Ch. 8.1 - Staining eukaryotic chromosomes is useful because...Ch. 8.2 - Prob. 1COMQCh. 8.3 - Which of the following statements is correct? a....Ch. 8.3 - Prob. 2COMQCh. 8.4 - 1. A paracentric inversion
a. includes the...Ch. 8.4 - Due to crossing over within an inversion loop, a...Ch. 8.4 - 3. A mechanism that may cause a translocation is...Ch. 8.5 - 1. Humans have 23 chromosomes per set. A person...Ch. 8.6 - Prob. 1COMQ
Ch. 8.6 - Prob. 2COMQCh. 8.7 - The term endopolyploidy refers to the phenomenon...Ch. 8.7 - 2. In agriculture, an advantage of triploidy in...Ch. 8.8 - Prob. 1COMQCh. 8.8 - The somatic cells of an allotetraploid contain a....Ch. 8 - 1. Which changes in chromosome structure cause a...Ch. 8 - Prob. 2CONQCh. 8 - 3. How does a chromosomal duplication occur?
Ch. 8 - 4. What is a gene family? How are gene families...Ch. 8 - Prob. 5CONQCh. 8 - Two chromosomes have the following orders for...Ch. 8 - An inversion heterozygote has the following...Ch. 8 - Prob. 8CONQCh. 8 - Explain why inversions and reciprocal...Ch. 8 - 10. An individual has the following reciprocal...Ch. 8 - A phenotypically normal individual has the...Ch. 8 - 12. Two phenotypically normal parents produce a...Ch. 8 - With regard to the segregation of centromeres, why...Ch. 8 - Prob. 14CONQCh. 8 - Prob. 15CONQCh. 8 - 16. A phenotypically abnormal individual has a...Ch. 8 - 17. A diploid fruit fly has eight chromosomes. How...Ch. 8 - Prob. 18CONQCh. 8 - Prob. 19CONQCh. 8 - 20. Aneuploidy is typically detrimental, whereas...Ch. 8 - 21. Explain how aneuploidy, deletions, and...Ch. 8 - Prob. 22CONQCh. 8 - 23. A cytogeneticist has collected tissue samples...Ch. 8 - Prob. 24CONQCh. 8 - A zookeeper has collected a male and a female...Ch. 8 - Prob. 26CONQCh. 8 - 27. What is mosaicism? How is it produced?
Ch. 8 - 28. Explain how polytene chromosomes of Drosophila...Ch. 8 - 29. Describe some of the advantages of polyploid...Ch. 8 - 30. While conducting field studies on a chain of...Ch. 8 - Prob. 31CONQCh. 8 - Which of the following terms should not be used to...Ch. 8 - Prob. 33CONQCh. 8 - Prob. 34CONQCh. 8 - A triploid plant has 18 chromosomes (i.e., 6...Ch. 8 - Prob. 36CONQCh. 8 - Prob. 37CONQCh. 8 - 38. A woman who is heterozygous, Bb, has brown...Ch. 8 - 39. What is an allodiploid? What factor determines...Ch. 8 - Prob. 40CONQCh. 8 - 41. Table 8.1 shows that Turner syndrome occurs...Ch. 8 - 42. Male honeybees, which are haploid, produce...Ch. 8 - Prob. 1EQCh. 8 - Prob. 2EQCh. 8 - With regard to the analysis of chromosome...Ch. 8 - 4. Describe how colchicine can be used to alter...Ch. 8 - 5. Describe the steps you would take to produce a...Ch. 8 - Prob. 6EQCh. 8 - What are G bands? Discuss how G bands are useful...Ch. 8 - A female fruit fly has one normal X chromosome and...Ch. 8 - Prob. 2QSDCCh. 8 - Besides the ones mentioned in this textbook, look...Ch. 8 - Prob. 4QSDCCh. 8 - 5. Discuss the importance of gene families at the...
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- In which of the following is genetic material moved betweennonhomologous chromosomes?a. insertion d. translocationb. nondisjunction e. inversionc. deletionarrow_forwardHow is homologous recombination for DNA repair different from recombination in meiosis? Choose all correct answers. a. HR in DNA repair requires a double-strand break, but meiotic recombination does not. b. HR in DNA repair requires strand invasion, but meiotic recombination does not. c. HR in DNA repair results in identical chromosomes. Meiotic recombination results in changes to the DNA sequence of the "repaired" chromosomes. d. HR in DNA repair uses a newly synthesized identical chromosome as a template. Meiotic recombination uses a homologous chromosome as a template.arrow_forwardUnder the influence of gamma-radiation a fragment of the chromosome was lost. What chromosomal mutation is it? Select one: a. Deletion. b. Duplication. c. Inversion. d. Intrachromosomal translocation. O e. Interchromosomal translocation.arrow_forward
- A mechanism that may cause a translocation isa. the joining of reactive ends when two different chromosomesbreak.b. crossing over between nonhomologous chromosomes.c. crossing over between homologous chromosomes.d. either a or b.arrow_forwardWhich of the following is not true in regard to crossover? a. Spindle microtubules guide the transfer of DNA across the synaptonemal complex. b. Nonsister chromatids exchange genetic material. c. Chiasmata are formed. d. Recombination nodules mark the crossover point.arrow_forwardCrossing over usually contributes to genetic variation by exchanging chromosomal segments between: A. nonhomologous loci of the genome (E) autosomes and sex chromosomes. B. chromatids of nonhomologous chromosomes C. non-sister chromatids of homologous chromosomes D. sister chromatids of a chromosome E. polyploid chromosomesarrow_forward
- Which of the following is a FALSE statement regarding human chromosomes? A. The chromosome number in humans is 2n=46. B. Gametes have half number of the chromosomes as in somatic cells. C. There are 22 pairs of autosomes and 2 sex chromosomes. D. Liver cells can be polyploids. They can have 23, 46, 69 or 92 chromosomes.arrow_forwardThe physical cause of the law of independent assortment for genes on the same chromosome is which of the following? Group of answer choices A. crossing over B. separation of homologous chromosomes in mitosis C.separation of sister chromatids in mitosis D. separation of sister chromatids in meiosis E. separation of homologous chromosomes in meiosisarrow_forwardUsing the symbols above: 1. Given: Adult diploid cell (2n = 8) 2. Show the condition of the chromosomes in the following Mitosis phases (illustrate): a. prophase b. metaphase c. anaphase d. telophase/cytokinesisarrow_forward
- When recombination (“crossing over”) doesn’t happen correctly, what type(s) of mutations that can occur? circle all that apply Select one or more: a. Inversion (reversal or “flipping” of part of a chromosome) b. Duplication of part of a chromosome c. Translocation (transfer of part of a chromosome to a non-homologous chromosome) d. Deletion of part of a chromosomearrow_forwardExamination of a karyotype reveals 23 pairs of chromosomes, with each homologous pair illustrating similar size and centromere location. Which of the following can be concluded from this karyotype?a. The individual has Down syndrome.b. The individual is a female.c. The individual does not have cystic fibrosis.d. The individual does not have sickle-cell anemia.arrow_forwardIn this image of the human karyotype: A. The sister chromatids have separated B. There are 46 pairs of chromosomes C. The DNA has already been replicated D. There are 23 pairs of autosomes E. None are true.arrow_forward
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