Genetics Exam 2 Flashcards

(31 cards)

1
Q
  1. A mutation in DNA that does not change the amino acid sequence of the resulting protein is
    a. impossible
    b. a missense mutation
    c. a nonsense mutation
    d. a silent mutation
A

d. a silent mutation

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2
Q
  1. A woman suffers from, and successfully recovers from skin cancer. The woman and her husband are trying to decide if they should have children. What is the likelihood their first child will have a higher than average likelihood of skin cancer?
    a. 50%
    b. 20%
    c. 12.5%
    d. 0%
A

d. 0% (Somatic mutation not heritable)

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3
Q
  1. A diploid somatic cell from a rat has a total of 42 chromosomes (2n = 42). What is the total number of chromosomes present in rat
    gametes?
    a. 21
    b. 42
    c. 84
    d. 126
    e. 168
A

a. 21

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4
Q
  1. Which of the following is the correct order of the phases in mitosis?
    a. Metaphase, Prophase, Interphase, Anaphase, Telophase
    b. Prophase, Metaphase, Anaphase, Telophase, Interphase
    c. Prophase, Metaphase, Interphase, Telophase, Anaphase
    d. Telophase, Anaphase, Prophase, Metaphase, Interphase
A

b. Prophase, Metaphase, Anaphase, Telophase, Interphase

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5
Q
  1. Which phase of the mitotic cell cycle has two identical copies of the genome in the cell for the entire phase?
    a. I
    b. S
    c. G2
    d. M
A

c. G2 (DNA has replicated, but mitosis hasn’t started)

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6
Q
  1. When do homologous chromosomes separate in meiosis?
    a. During prophase
    b. At anaphase I
    c. At anaphase II
    d. they don’t have to separate because they never pair up!
A

b. At anaphase I

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7
Q
  1. What is a tetrad?
    a. The four haploid products of meiosis
    b. Two pairs of sister chromatids
    c. The four kinetochores of paired homologous chromosomes
    d. The four nuclei that fuse during meiosis
A

b. Two pairs of sister chromatids (one from each homolog)

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8
Q
  1. Expanding nucleotide repeats such as CAGCAGCAGCAGCAG are often the result of_______.
    a. excess amounts of cytosine, adenine, and guanine in the cell.
    b. a slippage of the DNA template during replication.
    c. the movement of a transposon.
    d. reversion mutations.
A

b. a slippage of the DNA template during replication

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9
Q
  1. Base analogs are mutagenic because of which characteristic?
    a. They produce changes in DNA polymerase that cause it to malfunction.
    b. They distort the structure of DNA.
    c. They are similar in structure to the normal bases, but base pair differently.
    d. They chemically modify the normal bases.
A

c. They are similar in structure to the normal bases, but base pair differently

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10
Q
  1. Homologous chromosomes and sister chromatids differ in that
    a. homologous chromosomes arise from DNA replication and sister chromatids belong to siblings
    b Homologous chromosomes are the copies from each parent and sister chromatids belong to siblings.
    c. Homologous chromosomes are the copies from each parent and sister chromatids are the product of DNA replication of each
    homolog.
    d. Homologous chromosomes are the product of DNA replication of each homolog and sister chromatids are the copies from each
    parent.
A

c. Homologous chromosomes are the copies from each parent and sister chromatids are the product of DNA replication of each homolog

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11
Q
  1. Which statement is most correct?
    a. During interphase sister chromatids are present on different alleles
    b. During interphase different genes are present at the same locus on sister chromatids
    c. During interphase homologs are present on different alleles
    d. During interphase different alleles are present at the same locus on different homologs
A

d. During interphase different alleles are present at the same locus on different homologs

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12
Q
  1. Trisomy 21 is caused by ____________ during either meiosis I or meiosis II.
    a. crossing over
    b. nondisjunction
    c. chiasmata
    d. disjunction
A

b. nondisjunction

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13
Q
  1. In a germline cell there are two pairs of chromosomes (2N=4). F and f represent two different alleles (versions or variants) of one
    gene, and Q and q represent two different alleles of another gene. On one pair of chromosomes are the F & f alleles, and on the other
    pair of chromosomes are the Q and q alleles. If this cell divides normally to produce sperm, what are the possible sperm genotypes?
    A) F, f, Q, q
    B) Ff, Ff, Qq, Qq
    C) FQ, fq, Fq, fQ
    D) Ff, Qq, FQ, fq, Fq, fQ
A

C) FQ, fq, Fq, fQ (independent assortment)

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14
Q
  1. A mutation in DNA that changes a single amino acid of the resulting protein is
    a. impossible
    b. a missense mutation
    c. a nonsense mutation
    d. highly improbable
A

b. a missense mutation

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15
Q
  1. Suppose there are two genes on two different chromosomes, one gene called G and the other called D. An individual has the genotype
    Gg,Dd. Which of the following drawings correctly shows cells in this individual after DNA replication but before cell division of the first
    meiosis? Assume no recombination/crossing-over occurs between the homologs. Circle one.
A

a) Two chromosome pairs, each with two sister chromatids. Alleles are G/g and D/d – this is correct.15.

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16
Q
  1. Post-translational modifications of proteins that bind to DNA in eukaryotic cells including phosphorylation, methylation, and
    acetylation are known as_____________.
    a. mutagens
    b. the histone code
    c. enhancers
    d. insulators
A

b. the histone code

17
Q
  1. When do sister chromatids separate in meiosis?
    a. At anaphase I
    b. At anaphase II
    c. During prophase
    d. During cytokinesis
A

b. At anaphase II

18
Q
  1. When do homologous chromatids separate in meiosis
    a. At anaphase I
    b. At anaphase II
    c. During prophase
    d. During cytokinesis
A

a. At anaphase I

19
Q
  1. In eukaryotic cells the nuclear envelope separates the processes of transcription and translation. This allows eukaryotic cells to
    perform __________ before translation that enhances the number of different proteins that can be made from a specific gene.
    a. alternative splicing
    b. polyadenylation
    c. RNA capping
    d. all of the above
A

a. alternative splicing

20
Q
  1. You perform a CHIP (Chromatin Immunoprecipitation) assay to determine
    a. if there are chloroplast genes in a sample
    b. which DNA sequence a known transcription factor binds to in a genome.
    c. which transcription factor a fragment a known DNA fragment binds to in a cell.
    d. to see if gene regulatory networks are similar between two organisms.
A

b. which DNA sequence a known transcription factor binds to in a genome

21
Q
  1. Ploidy refers to the number of sets of chromosomes found in an organism. Most multicellular organisms are _____.
    a. haploid
    b. tetraploid
    c diploid
    d. polyploid
22
Q
  1. siRNAs act ____________________.
    a. to connect tRNAs and mRNAs in the ribosome
    b. to remove introns.
    c. to silence genes by turning over tRNA
    d. to silence genes by turning over mRNA
A

d. to silence genes by turning over mRNA

23
Q
  1. When considering the initiation of transcription, one often finds consensus sequences located in the region of the DNA where RNA
    polymerase(s) binds. What is a consensus sequence?
    a. GAGA
    b. GCATGCAT
    c. the most probable set of nucleotides at a functional position.
    d. any trinucleotide repeat
A

c. the most probable set of nucleotides at a functional position

24
Q
  1. The amount of a specific protein that accumulates in the cell can be regulated by___________________
    a. the amount of transcription.
    b. the amount of translation.
    c. the amount of protein turnover or proteolysis.
    d. the rate of mRNA degradation
    e. all of the above
A

e. all of the above

24
25. The MLH1 gene is located on chromosome 3 in humans and four different alleles have been identified. The maximum number of alleles a single normal individual can have is: a. 1 b. 2 c. 3 d. 4
b. 2 (One from each parent)
25
26. Chromatin structure plays a role in eukaryotic but not bacterial gene regulation. In general condensed chromatin represses gene expression; Chromatin structure must therefore be altered before transcription can take place. Chromatin structure is altered by________ a. chromatin- remodeling complexes. b. modification of histone proteins. c. changes to DNA methylation. d. all of the above.
d. all of the above
26
27. Humans have 23 pairs of chromosomes. If a human had 47 chromosomes that would be the result of______. a. Polyploidy b. Aneuploidy c. Triploidy d. Diploidy
b. Aneuploidy
27
28. ___________ means that all cells in an organism contain the same genetic information, or genome, and the ability to create a complete organism. a. Mitosis b. Meiosis c. Genomic equivalence c. aneuploidy
c. Genomic equivalence
28
29. Which of the following is most likely a loss of function mutation? a. silent b. missense c. nonsense d. transversion e. transposition
c. nonsense (Usually creates a premature stop codon)
29
30. Which of the following leads to gametes receiving incorrect numbers of chromosomes? a. apoptosis b. synapsis c. heterozygosity d. nondisjunction
d. nondisjunction
30
31. Describe in detail how one DNA repair mechanism works including the type of mutation does it repair. (10 pts.)
drawing Nucleotide Excision Repair (NER): NER repairs bulky lesions such as thymine dimers (caused by UV light). Steps: Damage recognized by protein complex. DNA is unwound around the lesion. Endonuclease cuts strand on both sides of damage. Damaged segment is removed. DNA polymerase fills in gap using complementary strand. DNA ligase seals the nick. Type of Mutation Repaired: Pyrimidine dimers and bulky chemical adducts.