Genetic Test 4 Ch. 14 Flashcards
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
Answer: E
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
Answer: D
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
Answer: C
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
Answer: B
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
Answer: C
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.
Answer: B
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
Answer: D
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
Answer: E
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
Answer: A
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.
Answer: E
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.
Answer: C
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
Answer: D
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
Answer: C
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
Answer: D
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
Answer: B