Genetics: Analysis and Principles
6th Edition
ISBN: 9781259616020
Author: Robert J. Brooker Professor Dr.
Publisher: McGraw-Hill Education
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Chapter 8.2, Problem 1COMQ
Summary Introduction
Introduction:
Changes in the chromosome structure can cause different mutations in the chromosome and they can have adverse effects on the pattern of chromosome, binding, and pairing. Mutationsin chromosome number can be deletion, duplication, inversion, and translocation.
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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
When the chromosomes of closely related species are compared,
a. the banding patterns are often similar.
b. a few structural alterations may be seen.
c. a change in chromosome number may be seen.
d. all of the above are commonly observed.
Which of the following is correct regarding polytene chromosomes?
options:
A.
Exposure to a sublethal dose of X-rays causes spontaneous mutations.
B.
Polytene chromosomes have been useful to observe specific bands correlated with individual genes.
C. Both A and B
D. None of the above
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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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
- During the molecular process of homologous recombinationbetween homologous chromosomes,a. a Holliday junction forms.b. branch migration occurs.c. a heteroduplex region forms.d. all of the above occur.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_forwardWhen recombination (“crossing over”) doesn’t happen correctly, what type(s) of mutations that can occur? Mark all that apply Select one or more: a. Deletion of part of a chromosome b. Translocation (transfer of part of a chromosome to a non-homologous chromosome) c. Duplication of part of a chromosome d.Inversion (reversal or “flipping” of part of a chromosome)arrow_forward
- 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, duplicationarrow_forwardIn which of the following is genetic material moved betweennonhomologous chromosomes?a. insertion d. translocationb. nondisjunction e. inversionc. deletionarrow_forwardErrors in crossing-over can happen when... Select one: a. Non-homologous chromosomes cross-over and recombine. b. Homologous chromosomes form chiasmata at the wrong (non-homologous) locations. c. Chromosome breakage during crossing-over results in a chromosome fragment getting added to a different (incorrect) chromosome. d. All of the abovearrow_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_forwardIn an organism’s genome, autosomes are a. the chromosomes that differ between the sexes. b. chromosomes that are involved in sex determination. c. only inherited from the mother (maternal inheritance). d. all of the chromosomes other than sex chromosomesarrow_forwardWhich 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_forward
- Which of the following situations does not describes a chromosomal mutation? Select one: a. A cytosine nucleotide is substituted for thymine nucleotide in a gene. b. A portion of Chromosome 4 is deleted during interphase of meiosis. c. The sister chromatids of Chromosome 18 do not separate during anaphase II. d. A section of Chromosome 17 is duplicated leading to problems in the peripheral nervous system.arrow_forwardTrisomy 18 (Edwards Syndrome) is identified by a karyotype that shows A. too few copies of chromosome 18. B. too many copies of chromosome 18. C. an inversion of genes on chromosome 18. D. a translocation between both chromosome 18.arrow_forwardA paracentric inversiona. includes the centromere within the inverted region.b. does not include the centromere within the inverted region.c. has two adjacent inverted regions.d. has an inverted region at the very end of a chromosome.arrow_forward
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