Genetic Test 4 Ch. 14 Flashcards

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1
Q

1) Before Muller’s discovery that radiation induces mutation, scientists had to work on spontaneous mutants that were found solely by phenotype differences in natural populations. Which of the features of Drosophila made it a fortuitous choice for Morgan and his colleagues?<br></br>A) both sexual and asexual reproduction<br></br>B) well- known biochemical pathways<br></br>C) especially high rate of mutation<br></br>D) having a long life cycle<br></br>E) large number of visible phenotypes

A

Answer: E

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2
Q

2) Genes for regulatory elements, such as creb, were found to be important in animal learning. Which of the following would increase the probability that such an element is studied throughout the animal kingdom?<br></br>A) the large number of copies of the creb gene within a genome<br></br> <br></br>B) its unique to Drosophila<br></br>C) the finding that creb activates odor perception<br></br>D) the finding that creb is highly conserved <br></br>E) the interaction of creb with cAMP

A

Answer: D

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3
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3) A researcher wants to mutagenize an organism. She is not in need of a large number of mutants but is more concerned with being able to find and then to amplify the mutated sequence. Which of the following would therefore be more useful?<br></br>A) a chemical mutagen<br></br> <br></br>B) UV radiation<br></br>C) transposon insertion<br></br>D) ionizing radiation<br></br>E) search for spontaneous mutant

A

Answer: C

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4
Q

4) In order to identify genes that function together in genetic pathways researchers can perform modifier screens, looking for second site enhancers or suppressors of a mutant. Which of the following is the most reasonable strategy for carrying out a suppressor screen in particular?<br></br>A) screen for enhancer- trap strains that show gene expression differences in the original mutant.<br></br>B) mutagenize the original mutant and look for new mutations that reduce the severity of the original mutant phenotype<br></br>C) isolate mutants with phenotypes similar to the original mutant phenotype and then cross the mutants to identify the affected gene(s)<br></br>D) identify mutations that, when crossed with the original mutant, result in synthetic lethality<br></br>E) analyze the DNA sequence near the mutation of interest, looking for sequences that may act as silencers

A

Answer: B

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5
Q

5) In Drosophila, mutation screening usually involves use of a balancer chromosome that includesthree elements: a set of overlapping inversions, an easily recognized dominant mutation, and a recessive lethal mutation that prevents balancer homozygotes from surviving. Which one, or combination, of these elements is necessary and sufficient to suppress crossovers?<br></br>A) lethal recessive<br></br> <br></br>B) inversions plus dominant C) inversions<br></br>D) lethal plus inversions<br></br>E) dominants

A

Answer: C

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6
Q

6) A mutagenesis screen provides 24 alleles shown by complementation analysis to be in the samegene, which of the following is true?<br></br>A) The gene, in whole or in part, must be involved in transformation.<br></br> <br></br>B) These mutants can be used to identify the function of this gene.<br></br>C) The gene being studied must be present in more than one copy per haploid genome.<br></br>D) The gene must be highly conserved in evolution.<br></br>E) The gene must be involved in regulating a signal pathway.

A

Answer: B

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7
Q

7) EMS (ethylmethane sulfonate) is mutagenic because ________.<br></br>A) it breaks phosphodiester bonds<br></br>B) it forms cross- links between DNA strands<br></br> <br></br>C) it makes DNA more susceptible to radiation<br></br>D) it adds alkyl groups to bases<br></br>E) it causes chromosomal deletions

A

Answer: D

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8
Q

8) Besides the obvious fact that chemical mutagens are dangerous to handle, another major disadvantage to their use is that ________.<br></br>A) chemical mutagens activate transposons which cause widespread genetic damage<br></br> <br></br>B) they alter all A- T and C- G base pairing<br></br>C) they often result in only dramatic alterations of gene function<br></br>D) most of these mutations are immediately lethal<br></br>E) most chemically induced changes are detectable only by genetic mapping and sequencing

A

Answer: E

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9
Q

9) The reasons for using transposon- based mutagenesis include all of the following EXCEPT________.<br></br>A) likely to cause only minimal effects on gene function<br></br>B) mutations are often ‘tagged’ by the nearby transposon<br></br>C) antibiotic selection can be employed during mutagenesis.<br></br>D) dramatic mutations which often cause null alleles E) transposons are found in nearly all organisms

A

Answer: A

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10
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10) A researcher is interested in testing the role for a highly- conserved amino acid in the function of a mouse protein. She has been unable to locate any pre- existing variants in this codon among a large<br></br> <br></br>number of available mouse strains. What might be her approach to generating such mutants? <br></br>A) Use RNAi to knockdown the expression of the target gene.<br></br>B) Use RNAi to interfere with translation of the gene.<br></br>C) Use transposons to generate insertion alleles in the gene.<br></br>D) Measure the expression of this gene in mice as they develop.<br></br>E) Use CRISPR- cas to cause DNA cleavage at the codon encoding this amino acid.

A

Answer: E

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11
Q

11) In a disease associated with a nucleotide repeat, anticipation is often noticed in subsequent generations, usually associated with a more severe phenotype. Which of the following is a more likely cause of anticipation?<br></br>A) Highly repeated sequences are expressed more often.<br></br> <br></br>B) Children of affected parents receive more attention from physicians than other children.<br></br>C) Alleles with a large number of repeats are unstable and change size from generation to generation.<br></br>D) The sequences have greater stability in later generations.<br></br>E) Family members are exposed to the same mutagens.

A

Answer: C

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12
Q

12) If you wish to use RNAi to reduce the expression of a gene in an organism. What would you inject into the organism?<br></br>A) Dicer with double- stranded (ds) DNA<br></br> <br></br>B) dsRNA including transposase<br></br>C) ssRNA complementary to cDNA<br></br>D) dsRNA homologous to the gene<br></br>E) ssRNA complementary to introns of the target gene

A

Answer: D

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13
Q

13) To introduce dsRNA into C. elegans, it is enough just to dip the worms into media that includes E.coli containing the dsRNA because ________.<br></br>A) C. elegans emit toxins that paralyze the bacteria<br></br> <br></br>B) E. coli infect C. elegans and then the RNA is released <br></br>C) C. elegans feed on the transgenic bacteria<br></br>D) E. coli DNA integrates into the genome of C. elegans<br></br>E) E. coli emit chemicals that cause pores to open in the nematode body wall

A

Answer: C

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14
Q

14) Which of the following tools/techniques would allow a researcher to measure the expression of a gene of interest in live organisms?<br></br>A) a lacZ reporter fused to the gene promoter<br></br>B) homologous recombination to replace the promoter of the gene of interest with a bacterial promoter<br></br>C) measuring the frequency of mutations by DNA sequencing<br></br>D) a transgene that fuses GFP to the gene of interest<br></br>E) RNAi targeting the promoter of the gene of interest

A

Answer: D

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15
Q

15) In reverse genetics, what is the correct order in which the experimenter proceeds?<br></br>A) selection of mutants with a phenotype of interest and then mapping to locate the effected gene(s)<br></br>B) identification of a gene of interest followed by screening for mutations in that gene and studies of the phenotypes caused those mutations.<br></br>C) random bombardment of the DNA with a known mutagen, followed by observation of offspring for newly acquired traits<br></br>D) screening individuals by PCR/DNA sequencing to associate altered genes with the trait of interest<br></br>E) silencing the genes in question using RNAi, followed by mapping to locate the gene

A

Answer: B

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16
Q

16) If a gene in Drosophila is expressed only in imaginal disc (A) when it begins to differentiate, it is referred to as a homeotic gene. Recessive mutations in such genes often result in loss of function so that the structure does not develop. If a transgenic organism is made in which the gene is expressed in a different imaginal, disc (B), what is the predicted result?<br></br>A) deregulation of gene expression throughout disc A<br></br>B) loss of function of disc B’s primary gene<br></br>C) gain of function of several inappropriate genes in disc A<br></br>D) deregulation of gene expression throughout disc B<br></br>E) gain of function in disc B of some of the structures usually seen in disc A

A

Answer: E

17
Q

17) A gene, VTE4, from the sunflower of known sequence and well- understood transcriptional regulation, is available from another lab. The product of this gene enables sunflowers to to produce a significantly increased amount of vitamin E from a substrate produced in all plants. The plant Brassica napus is harvested for canola oil. To produce canola oil with increased vitamin E, how would you proceed?<br></br>A) Clone VTE4 in A. tumefaciens and use these bacteria to produce transgenic Brassica.<br></br>B) Use a yeast system to engineer yeasts that produce the vitamin, and get manufacturers to add this to the canola oil during bottling.<br></br>C) Introduce the gene and necessary cis elements into Brassica, along with a reporter gene, then measure the vitamin E produced.<br></br>D) Introduce VTE4 into tomato plants or another food that humans eat more than Brassica.<br></br>E) Select Brassica plants with the highest titer of the vitamin, isolate the genes responsible, and cause these genes to duplicate.

A

Answer: C

18
Q

18) Identifying an autosomal recessive mutation in a mutagenic screen in Drosophila requires identification of a mutant in the F3 generation. If testing for a sex- linked recessive lethal mutation (e.g., cn l + using a balancer chromosome such as cnCyO), in which generation can lines with mutations be identified?

A

Answer: F2

19
Q

19) Which portion of a gene might you target with the CRISPR- cas system to interfere withsplicing?

A

Answer: intron/exon junction or splice site

20
Q

20) What kind of analysis is needed to determine whether two mutations are in the same geneor in different genes?

A

Answer: complementation

21
Q

21) In a given situation, reduced or missing function in gene A results in a viable but noticeable phenotype. The same is true for gene B. However, when both gene A and gene B products are reduced or missing in the same organism, the result is lethality. What is this called?

A

Answer: synthetic lethality or synthetic enhancement

22
Q

22) Suppose a scientist works with a mouse strain B75 and isolates an interesting recessive mutant that they call glyph. The researcher wants to identify the gene affected in glyph by complementation cloning. Which strain would the researcher use as the source of DNA for transformation?

A

Answer: the wild type strain B75

23
Q

23) In positional cloning, the researcher begins with a phenotype. To move toward identification of its DNA sequence, she must begin with what step?

A

Answer: genetic mapping

24
Q

24) DNA markers that are found to segregate with a mutation of interest can be used to determine the mutation’s distance from the markers by looking at what?

A

Answer: recombination frequency

25
Q

25) Which technique can be used to replace an endogenous gene with one constructed in vitro?

A

Answer: homologous recombination

26
Q

26) Libraries of insertion strains can be screened, primarily by which common technique, toidentify mutations in a gene of interest?

A

Answer: polymerase chain reaction or PCR

27
Q

27) In an organism, X, it is found to be impossible to generate loss- of- function mutants formost genes. There is an alternative method of introducing random mutations that can later be screened for the gene(s) in question. This can be accomplished by using insertions due to what genetic entities?

A

Answer: transposons or T- DNA

28
Q

28) What method allows researchers to reduce the expression of a target gene, even in wildtype organisms that have not previously been genetically modified?

A

Answer: RNA interference or RNAi

29
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29) In nature, RNAi protects cells against infection by what kind of pathogen?

A

Answer: dsRNA viruses or double- stranded RNA viruses

30
Q

30) Reporter genes such as GFP can be integrated into a native gene to study the expressionpattern of a target gene. If a researcher wishes to make a fusion of the GFP protein to the protein expressed by the target gene, where must the GFP gene integrate?

A

Answer: into the coding region or exon of the target gene

31
Q

31) The GFP gene is useful as a reporter gene because the cells and tissues with it emit fluorescence when treated with what, which functions as a substrate?

A

Answer: UV, purple, or blue light

32
Q

32) If an experimenter wants to use the GFP method but needs to detect the presence or absence of several proteins at the same time, he can take advantage of mutational variants of GFP that emit what?

A

Answer: other colors

33
Q

33) A genetic strategy that starts with knowing the DNA sequence and works toward identifying an associated phenotype is known as ________.

A

Answer: reverse genetics

34
Q

34) Chemical mutagens are preferred to ________ because they have a broader mutationspectrum, including generating alleles that affect only a single codon.

A

Answer: transposons or radiation

35
Q

35) A balancer chromosome includes a recessive lethal allele, a marker dominant allele, and ________.

A

Answer: inversion(s)

36
Q

36) A single nucleotide in a genome can be targeted for mutagenesis using the ________ technique, adapted from a bacterial defense system.

A

Answer: CRISPR- cas