Deck 8: Variation in Chromosome Structure and Number

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Question
Given the following sequence of genes on a chromosome,determine what change in chromosome structure occurred.The asterisk (*)indicates the centromere.
Before:A B C D * E F G H
After:A B C D * E F E F G H

A) terminal deficiency
B) interstitial deficiency
C) inversion
D) gene duplication
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Question
A translocation cross may occur in an individual which has which of the following?

A) reciprocal translocation
B) unbalanced translocation
C) simple translocations
D) All of these choices are correct.
Question
Which of following expressions denotes a trisomic organism?

A) 3n
B) 2n-1
C) 2n+1
D) 2n+2
Question
Examples of euploidy include

A) diploidy.
B) triploidy.
C) tetraploidy.
D) polyploidy.
E) aneuploidy.
Question
Inversion loops can occur in which of the following?

A) paracentric inversions
B) pericentric inversions
C) gene duplications
D) reciprocal translocations
E) both paracentric inversions and pericentric inversions
Question
The production of gene families,such as the globin genes,is the result of ________.

A) inversions
B) deficiencies
C) gene duplications
D) simple translocations
E) None of these choices are correct.
Question
Edward and Patau syndromes are examples of ________.

A) aneuploidy
B) allopolyploidy
C) autopolyploidy
D) translocations
Question
Which of the following would have the shortest p arm of the chromosome?

A) acrocentic
B) metacentric
C) telocentric
D) submetacentric
Question
The effects of a deficiency on an organism are dependent on the importance of the missing genetic material.
Question
Inversions are contained within what percent of the human population?

A) less than 1%
B) approximately 2%
C) approximately 5%
D) greater than 10%
Question
Which of the following generally has the least effect on the phenotype of the individual who carries it?

A) Robertsonian translocation
B) unbalanced translocation
C) balanced translocation
D) All of these choices are equally detrimental to the phenotype.
Question
Robertsonian translocations usually occur between what types of chromosomes?

A) metacentric
B) acrocentric
C) telocentric
D) submetacentric
Question
Given the following sequence of genes on a chromosome,determine what change in chromosome structure occurred.The asterisk (*)indicates the centromere.
Before:A B C D * E F G H
After:A B G F E * D C H

A) reciprocal translocation
B) pericentric inversion
C) paracentric inversion
D) gene duplication
E) None of the answers are correct.
Question
What causes gene duplications?

A) the crossing over of misaligned chromosomes
B) deletion of important genetic information
C) reciprocal translocations
D) position effect
E) None of these choices are correct.
Question
An inversion heterozygote contains which of the following?

A) two homologous chromosomes with inversions
B) two normal chromosomes
C) one normal chromosome and one chromosome with an inversion
D) None of these choices are correct.
Question
What process is the cause of human genetic diseases such a cri-du-chat (or Lejeune)syndrome?

A) translocation
B) duplication
C) deletion
D) inversion
Question
Chromosomes may be identified based on which of the following characteristics?

A) location of the centromere
B) banding patterns
C) size of the chromosome
D) All of these choices are correct.
Question
Variations in chromosome structure are important for which of the following reason(s)?

A) evolution of new species
B) may result in the production of abnormal offspring
C) may alter the phenotype of an organism
D) All of these choices are correct.
Question
A loss of an internal portion of a chromosome is called a(n)________.

A) reciprocal translocation
B) terminal deficiency
C) interstitial deletion
D) gene duplication
Question
Given the following sequence of genes on a chromosome,determine what change in chromosome structure occurred.The asterisk (*)indicates the centromere.
Before: A B C D * E F G H
After:A C D * E F G H

A) terminal deletion
B) interstitial deletion
C) inversion
D) gene duplication
Question
Due to the formation of an inversion loop,sections of DNA may either be duplicated or deleted.
Question
_______ is a drug that is used to experimentally produce polyploidy in organisms.

A) Penicillin
B) Colchicine
C) Polymosca
D) Karyocine
Question
The failure of chromosomes to separate during anaphase is called ________.

A) synapsis
B) maternal effect
C) epistasis
D) nondisjunction
Question
The short arm of a chromosome is denoted by the letter ________ and the long arm by the letter ________.

A) p; q
B) s; l
C) q; p
D) c; d
Question
What are Klinefelter and Turner syndromes examples of?

A) sex chromosome aneuploidy
B) autosomal aneuploidy
C) reciprocal translocations
D) paracentric inversions
Question
The polytene chromosomes of Drosophila are an example of ________.

A) aneuploidy
B) polyploidy
C) translocations
D) inversion loops
E) None of these choices are correct.
Question
Variations in a gene are called allelic variations.
Question
Which type of plant would usually be a seedless variety?

A) aneuploid
B) diploid
C) triploid
D) tetraploid
Question
A ________ translocation occurs when a piece of one chromosome is attached to another chromosome.

A) simple
B) complex
C) reciprocal
D) balanced
Question
The ends of chromosomes have areas of repeated DNA called centromeres.
Question
The majority of autosomal aneuploid conditions are lethal,but sex chromosome aneuploids are usually not lethal.
Question
Which of the following describes an organism with two complete sets of chromosomes from two different species?

A) tetraploid
B) aneuploid
C) allodiploid
D) allotetraploid
Question
Since no genetic material is lost or gained by an inversion,it will only influence phenotype if the breaks are within a gene or in important regulatory regions for a gene.
Question
Which correctly describes mitotic nondisjunction?

A) It is a relatively rare event.
B) It results in the loss of chromosomes in some cells.
C) It usually does not affect all of the cells of the organism.
D) All of these choices are correct.
Question
Homologous genes within a species are called paralogs.
Question
Select the pairs that correctly match an aneuploid condition to its genotype.

A) Edward syndrome - trisomy 18
B) Down syndrome - trisomy 21
C) Jacobs syndrome - XYY
D) Turner syndrome - XXY
E) Klinefelter - XO 
Question
The term ________ refers to genetic differences between members of the same species.

A) chromosomal variation
B) genetic variation
C) chromosomal deletions
D) polyploidy
Question
Which human cells exhibit endopolyploidy?

A) sex cells
B) nerve cells
C) all somatic cells
D) liver cells
E) red blood cells
Question
Polyploid plants tend to produce less fruits and flowers,be smaller in size,and cannot adapt as well to extreme environmental conditions as normal varieties.
Question
Inversions represent a change in the total genetic material of a chromosome.
Question
Polytene chromosomes are

A) chromosomes that lack telomeres.
B) chromosomes with high copy number variation.
C) backup copies of chromosomes that are kept segregated away from the functional copies.
D) bundles of hundreds of copies of the same chromosome.
Question
If a disease is associated with copy number variation,that suggests that it is caused by the presence of

A) mRNA transcripts missing the translation STOP sequence.
B) a much longer version of a gene.
C) a duplicated or deleted copy of a gene.
D) extra telomeres.
Question
Describe endopolyploidy,and how it might benefit an organism.

A) Portions of the organism have extra copies of all chromosomes, for producing additional gene products.
B) The entire organism has extra copies of certain chromosomes, for producing additional gene products.
C) The entire organism has extra copies of all chromosomes, to act as backup in case of DNA damage.
D) Portions of the organism have extra copies of certain genes, for the functions of specialized cell types.
Question
Genetic abnormalities that occur after fertilization may result in some tissues of the body differing in their genetic composition.This is called ________.

A) mosaicism
B) polyploidy
C) polypheny
D) genetic variation
Question
Visible or measurable characteristics of an organism,resulting from its genotype,are called its ________.
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Deck 8: Variation in Chromosome Structure and Number
1
Given the following sequence of genes on a chromosome,determine what change in chromosome structure occurred.The asterisk (*)indicates the centromere.
Before:A B C D * E F G H
After:A B C D * E F E F G H

A) terminal deficiency
B) interstitial deficiency
C) inversion
D) gene duplication
D
2
A translocation cross may occur in an individual which has which of the following?

A) reciprocal translocation
B) unbalanced translocation
C) simple translocations
D) All of these choices are correct.
A
3
Which of following expressions denotes a trisomic organism?

A) 3n
B) 2n-1
C) 2n+1
D) 2n+2
C
4
Examples of euploidy include

A) diploidy.
B) triploidy.
C) tetraploidy.
D) polyploidy.
E) aneuploidy.
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Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
5
Inversion loops can occur in which of the following?

A) paracentric inversions
B) pericentric inversions
C) gene duplications
D) reciprocal translocations
E) both paracentric inversions and pericentric inversions
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Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
6
The production of gene families,such as the globin genes,is the result of ________.

A) inversions
B) deficiencies
C) gene duplications
D) simple translocations
E) None of these choices are correct.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
7
Edward and Patau syndromes are examples of ________.

A) aneuploidy
B) allopolyploidy
C) autopolyploidy
D) translocations
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Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
8
Which of the following would have the shortest p arm of the chromosome?

A) acrocentic
B) metacentric
C) telocentric
D) submetacentric
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Unlock Deck
k this deck
9
The effects of a deficiency on an organism are dependent on the importance of the missing genetic material.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
10
Inversions are contained within what percent of the human population?

A) less than 1%
B) approximately 2%
C) approximately 5%
D) greater than 10%
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
11
Which of the following generally has the least effect on the phenotype of the individual who carries it?

A) Robertsonian translocation
B) unbalanced translocation
C) balanced translocation
D) All of these choices are equally detrimental to the phenotype.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
12
Robertsonian translocations usually occur between what types of chromosomes?

A) metacentric
B) acrocentric
C) telocentric
D) submetacentric
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Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
13
Given the following sequence of genes on a chromosome,determine what change in chromosome structure occurred.The asterisk (*)indicates the centromere.
Before:A B C D * E F G H
After:A B G F E * D C H

A) reciprocal translocation
B) pericentric inversion
C) paracentric inversion
D) gene duplication
E) None of the answers are correct.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
14
What causes gene duplications?

A) the crossing over of misaligned chromosomes
B) deletion of important genetic information
C) reciprocal translocations
D) position effect
E) None of these choices are correct.
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Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
15
An inversion heterozygote contains which of the following?

A) two homologous chromosomes with inversions
B) two normal chromosomes
C) one normal chromosome and one chromosome with an inversion
D) None of these choices are correct.
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Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
16
What process is the cause of human genetic diseases such a cri-du-chat (or Lejeune)syndrome?

A) translocation
B) duplication
C) deletion
D) inversion
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Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
17
Chromosomes may be identified based on which of the following characteristics?

A) location of the centromere
B) banding patterns
C) size of the chromosome
D) All of these choices are correct.
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Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
18
Variations in chromosome structure are important for which of the following reason(s)?

A) evolution of new species
B) may result in the production of abnormal offspring
C) may alter the phenotype of an organism
D) All of these choices are correct.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
19
A loss of an internal portion of a chromosome is called a(n)________.

A) reciprocal translocation
B) terminal deficiency
C) interstitial deletion
D) gene duplication
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
20
Given the following sequence of genes on a chromosome,determine what change in chromosome structure occurred.The asterisk (*)indicates the centromere.
Before: A B C D * E F G H
After:A C D * E F G H

A) terminal deletion
B) interstitial deletion
C) inversion
D) gene duplication
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
21
Due to the formation of an inversion loop,sections of DNA may either be duplicated or deleted.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
22
_______ is a drug that is used to experimentally produce polyploidy in organisms.

A) Penicillin
B) Colchicine
C) Polymosca
D) Karyocine
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
23
The failure of chromosomes to separate during anaphase is called ________.

A) synapsis
B) maternal effect
C) epistasis
D) nondisjunction
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Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
24
The short arm of a chromosome is denoted by the letter ________ and the long arm by the letter ________.

A) p; q
B) s; l
C) q; p
D) c; d
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Unlock Deck
k this deck
25
What are Klinefelter and Turner syndromes examples of?

A) sex chromosome aneuploidy
B) autosomal aneuploidy
C) reciprocal translocations
D) paracentric inversions
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Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
26
The polytene chromosomes of Drosophila are an example of ________.

A) aneuploidy
B) polyploidy
C) translocations
D) inversion loops
E) None of these choices are correct.
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Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
27
Variations in a gene are called allelic variations.
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Unlock Deck
k this deck
28
Which type of plant would usually be a seedless variety?

A) aneuploid
B) diploid
C) triploid
D) tetraploid
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
29
A ________ translocation occurs when a piece of one chromosome is attached to another chromosome.

A) simple
B) complex
C) reciprocal
D) balanced
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
30
The ends of chromosomes have areas of repeated DNA called centromeres.
Unlock Deck
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Unlock Deck
k this deck
31
The majority of autosomal aneuploid conditions are lethal,but sex chromosome aneuploids are usually not lethal.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
32
Which of the following describes an organism with two complete sets of chromosomes from two different species?

A) tetraploid
B) aneuploid
C) allodiploid
D) allotetraploid
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
33
Since no genetic material is lost or gained by an inversion,it will only influence phenotype if the breaks are within a gene or in important regulatory regions for a gene.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
34
Which correctly describes mitotic nondisjunction?

A) It is a relatively rare event.
B) It results in the loss of chromosomes in some cells.
C) It usually does not affect all of the cells of the organism.
D) All of these choices are correct.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
35
Homologous genes within a species are called paralogs.
Unlock Deck
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Unlock Deck
k this deck
36
Select the pairs that correctly match an aneuploid condition to its genotype.

A) Edward syndrome - trisomy 18
B) Down syndrome - trisomy 21
C) Jacobs syndrome - XYY
D) Turner syndrome - XXY
E) Klinefelter - XO 
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
37
The term ________ refers to genetic differences between members of the same species.

A) chromosomal variation
B) genetic variation
C) chromosomal deletions
D) polyploidy
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
38
Which human cells exhibit endopolyploidy?

A) sex cells
B) nerve cells
C) all somatic cells
D) liver cells
E) red blood cells
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
39
Polyploid plants tend to produce less fruits and flowers,be smaller in size,and cannot adapt as well to extreme environmental conditions as normal varieties.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
40
Inversions represent a change in the total genetic material of a chromosome.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
41
Polytene chromosomes are

A) chromosomes that lack telomeres.
B) chromosomes with high copy number variation.
C) backup copies of chromosomes that are kept segregated away from the functional copies.
D) bundles of hundreds of copies of the same chromosome.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
42
If a disease is associated with copy number variation,that suggests that it is caused by the presence of

A) mRNA transcripts missing the translation STOP sequence.
B) a much longer version of a gene.
C) a duplicated or deleted copy of a gene.
D) extra telomeres.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
43
Describe endopolyploidy,and how it might benefit an organism.

A) Portions of the organism have extra copies of all chromosomes, for producing additional gene products.
B) The entire organism has extra copies of certain chromosomes, for producing additional gene products.
C) The entire organism has extra copies of all chromosomes, to act as backup in case of DNA damage.
D) Portions of the organism have extra copies of certain genes, for the functions of specialized cell types.
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
44
Genetic abnormalities that occur after fertilization may result in some tissues of the body differing in their genetic composition.This is called ________.

A) mosaicism
B) polyploidy
C) polypheny
D) genetic variation
Unlock Deck
Unlock for access to all 45 flashcards in this deck.
Unlock Deck
k this deck
45
Visible or measurable characteristics of an organism,resulting from its genotype,are called its ________.
Unlock Deck
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Unlock Deck
k this deck
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