Deck 19: Genomes and Proteomes

Question 1

Which pre-mRNA processing mechanism allows different proteins to be produced from the same DNA sequence? ​

A)transposition
B)alternative splicing
C)intron shuffling
D)intron splicing
E)open reading frame shuffling

Answer 1

B

Question 2

The human genome is composed of approximately _____ billion base pairs.

A)1
B)​3
C)​7
D)​10
E)​14

Answer 2

B

Question 3

When the human genome was sequenced, we learned that there are fewer than expected protein coding genes (approximately 20,000). Yet, the total number of proteins produced in humans approaches 100,000. What accounts for this discrepancy in numbers?

A)We have not yet identified all of the open reading frames in the human genome.
B)We have not yet fully sequenced the human genome.
C)mRNA processing mechanisms allowmultiple proteins to be produced from a single DNA sequence.
D)Some noncoding DNA sequences encode proteins.
E)There has been a gross over-estimation of the number of proteins produced in humans.

Answer 3

C

Question 4

The chemical difference between dideoxyribonucleotides used in Sanger sequencing and the deoxyribonucleotides normally found in DNA is the presence of a(n)_____ in the deoxyribose sugar of dideoxyribonucleotides.

A)3' - H rather than - OH ​
B)5' - H rather than - OH
C)5' - OH rather than - H
D)5'  - H rather than - OH
E)3' - COOH rather than - OH

Question 5

The percentage of the human genome that is protein-coding is less than _____. ​

A)2%
B)20%
C)30%
D)50%
E)85%

Question 6

A scientist obtains the DNA sequence datafor a bacterial plasmid. The data includes As, Ts, and Gs, but no Cs.  What is the most likely cause of this result? ​

A)ddCs were omitted from the sequencing reaction.
B)The cytosine deoxyribonucleotides were omitted from the sequencing reaction.
C)DNA polymerase was omitted from the sequencing reaction mix.
D)The ddG fluorescent tags were degraded.
E)There is no cytosine in this DNA molecule.

Question 7

Which domain(s)have densely packed genomes with little noncoding space? ​

A)Archaea only
B)Bacteria only
C)Eukarya only
D)Archaea and Eukarya
E)Bacteria and Archaea

Question 8

In humans, the majority of a transcription unit is composed of ____.

A)exons
B)introns
C)promoter regions ​
D)start codons
E)regulatory elements

Question 9

The Human Genome Project completed in 2003 focused on sequencing the genome(s)of _____.

A)the mouse only
B)humans only
C)bacteria only
D)humans and prokaryotes only
E)humans and other model organisms

Question 10

What is a difference between human male and female genomes? ​

A)Males have 46 chromosomes; females have 45.
B)Males have 22 pairs of autosomal chromosomes; females have 21 pairs of autosomal chromosomes.
C)Males have 23 pairs of chromosomes plus 1 Y chromosome; females have 23 pairs of chromosomes.
D)Males have 24 different chromosomes; females have 23 different chromosomes
E)Males have an X chromosome; females do not.

Question 11

Which study indicates that some mutations are inherited from our parents?

A)study of mutations in nerve cells
B)study of mutations in somatic cells
C)study of mutations in germline cells
D)study of mutations in premature infants
E)study of mutations in in vitro babies

Question 12

How do scientists most often access genome sequences determined by research projects?

A)They must request the sequence from the group that performed the research.
B)They must request the sequence from the governmental or private group that funded the research.
C)They must request the sequence from the company that performed the sequencing.
D)They can retrieve the sequence from an online public database, such as GenBank.
E)They must sequence the organism themselves to obtain the sequence.

Question 13

In the whole-genome shotgun method, the genome is fragmented and individual fragments are sequenced. How is the order of the nucleotides determined for the original intact chromosome? ​

A)The fragmentation is done in a systematic way such that the physical arrangement of fragments is readily apparent.
B)The random fragmentation produces overlapping sequencesthat can be aligned and assembled to generate the original intact DNA molecule.
C)We supplement our information with data from a different technique to determine the final chromosome arrangement.
D)DNA hybridization assays are conducted to determine the physical arrangement of the genes on the chromosome.
E)After sequencing, the fragments are labeled and used as probes in a microarray.

Question 14

Deoxyribonucleotidesare included in the Sanger sequencing reaction mix to _____.

A)provide a substrate forRNA polymerase ​
B)enhance the activity of the dideoxyribonucleotides
C)allow longer DNA fragments (up to 300 additional base pairs)to be sequenced
D)allow the production of multiple DNA fragments of different lengths
E)prevent the DNA polymerase from making too many errors

Question 15

In whole-genome shotgun sequencing, ____.

A)DNA is broken into many random, overlapping fragments that are sequenced and then assembled using computer algorithms
B)whole chromosomes are sequencedintact from the 3'end to the 5' end
C)whole chromosomes are sequenced intactfrom the 5'end to the 3' end
D)DNA is broken into a few, non-overlapping fragments that can be read directly by computer algorithms
E)DNA is broken into individual nucleotides that are sequenced and then assembled using computer algorithms

Question 16

Which element of a dideoxy sequencing reaction allows for visualization ofthe DNA sequence? ​

A)the mixture of the four dideoxyribonucleotides, each with a different fluorescent label
B)DNA primer
C)the mixture of the four deoxyribonucleotides
D)DNA polymerase
E)DNA ligase

Question 17

To study how genes have evolved, scientists compare the genome sequences of related organisms, a research approach known as _____.

A)genome sequence determination
B)genome annotation
C)comparative genomics
D)functional genomics
E)proteomics ​

Question 18

What marks the 5 ¢ end of an ORF in a DNA sequence? ​

A)the stop codon TAG
B)the stop codon TAA
C)the start codon AUG
D)the start codon ATG
E)the promoter region containing a consensus sequence ​

Question 19

What is an open reading frame (ORF)? ​

A)a protein coding sequence plus associated regulatory sequences
B)the sequence between and including a start codon and an stop codon
C)the sequence between and including a start codon and an stop codon, minus the introns
D)the sequence between and including a start codon and an stop codon, minus the exons
E)the sequence between a start codon and stop codon in prokaryotes only

Question 20

During a DNA sequencing experiment, the researcher adds all the required components to the reaction but accidentally adds only one of the four dideoxynucleotides, the ddC. What products will be observed after this reaction is complete?

A)All fragments will end in A. ​
B)All fragments will end in C.
C)All fragments will end in G.
D)All fragments will end in T.
E)No fragments will be made.

Question 21

During DNA sequence annotation, which feature is not identified? ​

A)protein coding genes
B)noncoding RNA genes ​
C)origins of replication
D)pseudogenes
E)protein interactions

Question 22

How can microarrays help us understand cellular functions?

A)Microarrays let us study different cellular structures under different conditions.
B)Microarrays let us directly measure protein expression in individual cells.
C)Microarrayslet us identify which portions of a genome were being expressed in a cell at a particular time.
D)Microarrays let us identify which DNA sequences are present in a particular cell type under certain conditions.
E)Microarrays let us identify which portions of a genome serve as regulatory sequences.

Question 23

What is directly sequenced in RNA-seq? ​

A)protein
B)transcripts ​
C)RNA
D)DNA
E)cDNA

Question 24

A sequence similarity search reveals that a candidate gene's sequence has a partial match to a known gene's sequence. What does this most likely indicate? ​

A)There is no relationship between the candidate and known gene.
B)The candidate gene encodes an identical transcript to the known gene.
C)The candidate gene encodes the same protein as the known gene.
D)The protein encoded by the candidate gene contains a protein domain also found in the known gene's protein.
E)The protein encoded by the candidate gene has the same function as the protein encoded by the known gene.

Question 25

What can be removed from pre-mRNA during alternative splicing? ​

A)exons and ribosomal binding sites ​
B)ribosomal binding sites
C)exons only
D)introns only
E)exons and introns

Question 26

A researcher wants to investigate the function of a gene without permanently altering the gene's function or activity. Which experimental approach should she choose?

A)gene knockout
B)gene knockdown
C)electrophoresis
D)RNA-seq
E)bioinformatics

Question 27

A researcher obtains the results of his RNA-seq analysis. Several transcripts are listed as being derived from the same gene. How is this possible? ​

A)Alternative splicing allows for different transcripts to be created by the same gene sequence.
B)The researcher's sample was contaminated.
C)Exon shuffling allows for different transcripts to be created by the same gene sequence.
D)Intron shuffling allows for different transcripts to be created by the same gene sequence.
E)It is not possible; there was an error in the alignment process.

Question 28

Protein-coding ORFsare easier to identify in which type of organism? ​

A)eukaryotes because they have easily identifiable regulatory regions ​
B)eukaryotes because they have fewer introns
C)prokaryotes because they have few introns
D)eukaryotes because they have more exons
E)prokaryotes because they have more exons

Question 29

A gene encoding a subunit of hemoglobin in humans is found to be homologous to a gene in chimpanzees. The homologous gene in chimpanzees likely _____. ​

A)is a pseudogene
B)encodes the same hemoglobin subunit
C)is inactive because it is in a different species
D)is a regulatory sequence
E)encodes a respiratory enzyme

Question 30

A(n)_____ has a DNA sequence similar to a functional gene but has been mutated so that it no longer produces a functional gene product. ​

A)pseudogene
B)homologous gene
C)orthologous gene
D)microRNA-encoding sequence
E)operon

Question 31

Which field of study applies mathematics and computer science to gain information from biological data, such as data related to gene structure and function?

A)computer forensics ​
B)statistical biology
C)bioinformatics
D)genome sampling
E)metagenomics

Question 32

Through a sequence similarity search, a researcher identifies a gene whose predicted protein product has a putative function of a photosynthesis-enhancing enzyme. Which experimental method could be performed to verify this function? ​

A)PCR
B)an assay measuring photosynthetic productivity
C)identification of signature genes
D)DNA microarray
E)gene knockout

Question 33

Which technique can most accurately quantify RNA and determine levels of gene expression? ​

A)RNA-seq
B)microarray analysis
C)Illumina/Solexa sequencing
D)alignment searches
E)Sanger sequencing

Question 34

Which organism has the largest number of protein-coding genes? ​

A)E. coli (bacteria)​
B)Saccharomyces cerevisiae (yeast)
C)Homo sapiens (human)
D)Oryza sativa (rice)
E)Drosophila melanogaster (fruit fly)

Question 35

Which eukaryotic organelle(s)contain its/their own DNA?

A)chloroplasts only
B)endoplasmic reticulum only
C)mitochondria only ​
D)mitochondria and chloroplasts ​
E)mitochondria and endoplasmic reticulum

Question 36

RNA-seq (whole-transcriptome sequencing)_____.

A)is a new hybridization technique used in transcriptomics
B)is the most common method used to identify certain cancer genes
C)identifies and quantifies RNA transcripts in a sample
D)is being replaced by DNA microarrays in transcriptomics
E)can only identify 100 sequences at a time

Question 37

Many cancers can be identified based on microarray analysis of _____. ​

A)signature genes
B)genes in red blood cells
C)mitochondrial DNA
D)Y chromosome DNA
E)DNA probes ​

Question 38

The study of gene function by observing changes in phenotype is termed _____. ​

A)phenomics
B)genomics
C)mutagenomics
D)proteomics
E)transcriptomics

Question 39

RNAi is commonly used in which experimental strategy?

A)gene overexpression
B)DNA sequencing
C)gene knockout
D)gene knockdown
E)microarray analysis

Question 40

In the microarray shown in the textbook, the cDNAs were labeled with red and green fluorescent tags. Why do some spots on the microarray emit yellow light?

A)Red and green are two of the primary colors, and if both cDNAs hybridize to the spot, the combination of the two will produce yellow light.
B)The yellow light comes from the laser, and a yellow spot indicates that neither cDNA hybridized to that spot on the microarray.
C)The over expression of one cDNA relative to the other will skew the color pattern of the spot on the microarray, resulting in the yellow color.
D)The color choice was an arbitrary decision by the artist and doesn't reflect how the process actually works.
E)Yellow spots are those that contain no DNA probes on the chip.

Question 41

The goal(s)of proteomics include(s)the determination of protein_____. ​

A)structure only
B)function only
C)location only
D)sequence, interactions, and structure
E)structure, function, location, and interactions

Question 42

Gene duplication can result from _____.

A)a normal crossover event
B)exon shuffling ​
C)unequal crossing over
D)a point mutation
E)alternative splicing

Question 43

DNA microarrays that reveal differential expression patterns are used to study the _____. ​

A)genome
B)transcriptome
C)proteome
D)interactome
E)ribosome

Question 44

What has been learned from comparative genomics studies? ​

A)Similar genes in different organisms perform very different functions.
B)Prokaryotic DNA has different nucleotide bases compared to eukaryotic DNA.
C)Similar genes do not exist in different species.
D)Some genes are present in the genomes of almost all present-day organisms.
E)Different species can have identical genome sequences.

Question 45

A portion of a microarray is shown above in which the expression of genes on human chromosome 21 was examined in normal brain cells (cDNAs labeled with a white fluor)or brain cells from an individual with a neurological disorder (cDNAs labeled with a black fluor).
Which genes are over-expressed in the abnormal cells compared to the normal cells? ​

A)A2, B1, B3, and C4
B)B2 and C1
C)A1, A3, A4, B4, C2, and C3
D)A1, A2, B2, and C1
E)A2, C2, and C4

Question 46

Which gene would most likely be found in the genomes of all present-day organisms?

A)an amino-acyl tRNA synthetase gene ​
B)a photosynthetic gene
C)a nitrogen fixation gene
D)a gene for anaerobic respiration
E)a gene for cellulose breakdown

Question 47

When copies of a gene are found at different locations on the same or different chromosomes, the phenomenon is called _____.

A)dispersed duplication ​
B)dispersed localization
C)duplicate localization
D)gene dispersion
E)random dispersion

Question 48

The _____ techniqueis most effective for transcriptomics studies in non-model organisms because _____. ​

A)DNA microarray; DNA sequences from related organisms can be used as probes.
B)RNA-seq;it is less expensive
C)DNA microarray; prior knowledge about the genome sequence is not required.
D)RNA-seq; the probes used are smaller than those for DNA microarrays.
E)DNA microarray; fluorescence gives the best indication of gene activity.

Question 49

Protein structure can be predicted nonexperimentally by ____. ​

A)microscopy
B)nuclear magnetic resonance ​
C)X-ray crystallography
D)computer algorithms based on amino acid chemistry
E)electrophoresis

Question 50

Which event can introduce a protein domain into a pre-existing protein? ​

A)gene alignment
B)intron shuffling
C)exon shuffling
D)peptide shuffling
E)exon splicing

Question 51

To experimentally determine the function of an annotated gene, a researcher may _____. ​

A)look for similar gene sequences of known function
B)examine the putative protein structure
C)perform a gene knockout
D)find a pseudogene for the gene
E)determine the amino acid sequence

Question 52

Researcher A studies the protein interactions involving the polypeptides that comprise hemoglobin, while Researcher B studies protein interactions between a protein kinase and its target protein. Researcher A will therefore focus on ____, and researcher B will focus on ____. ​

A)protein localization; protein sequence
B)protein sequence; protein localization
C)permanent protein interactions; transient protein interactions
D)transient protein interactions; permanent protein interactions
E)protein regulation; transcriptional regulation

Question 53

How might a researcher best determine the location of a protein in a cell? ​

A)studying the amino acid sequence of the protein ​
B)fusing a fluorescent tag to the protein to visualize its cellular location under a microscope
C)attaching an antibiotic tag to the protein and determining its location using DNA microarrays
D)analyzing the untranslated regions of the gene encoding the protein
E)understanding the protein's function

Question 54

The proteome represents _____, while the cellular proteome represents _____. ​

A)all of the proteins able to be made by all living organisms; the proteins made by unicellular organisms
B)the set of proteins made by any multicellular organism; the set of proteins made by unicellular organisms
C)all of the proteins able to be expressed by an organism's genome; the subset of proteins found in a particular cell type
D)all of the proteins that are common to all living organisms; the proteins found in the same cell types of different species
E)the subject of proteomics research; the subject of phenomics research

Question 55

Unequal crossing over _____. ​

A)is an abnormal crossover event that occurs during mitosis ​
B)occurs between different points on homologous chromosomes
C)generates a single point mutation
D)is the result of alternative splicing
E)occurs between heterologous chromosomes

Question 56

Proteomics _____. ​

A)refers to the analysis of the entire protein content of a cell ​
B)refers to the analysis of all the DNA of a species
C)looks only at plasmids
D)studies mRNA levels
E)uses DNA chips

Question 57

In humans, there are three genes encoding different nitric oxide synthase enzymes. These three genes form a ____. ​

A)multigene locus ​
B)replicate gene family
C)multi-enzyme family
D)multigene family
E)gene grouping

Question 58

During a microarray analysis, cDNAs made from normal cells are stained with a green fluor and cDNAs from abnormal cells are stained with a red fluor. Which of the following statements is true about the results of this experiment?

A)Red spots indicate genes that are under expressed in abnormal cells.
B)Red spots indicate genes that are not expressed in abnormal cells.
C)Red spots indicate genes that are overexpressed in abnormal cells.
D)Red spots indicate genes that are overexpressed in normal cells.
E)Red spots indicate pseudogenes.

Question 59

Multigene families arise from _____. ​

A)a single gene duplication event
B)repeated cycles of gene duplication followed by mutation
C)single point mutations
D)exon shuffling
E)deletions of genes

Question 60

Genes that are closely related evolutionarily, have the same function, and are present in the genomes oftwo or more different organisms are called _____.

A)genologs ​
B)heterologs
C)Paralogs
D)Metalogs
E)orthologs

Question 61

A researcher obtains a sequence of a gene of interest including the ORF, 5 ¢ untranslated region, and 3 ¢ untranslated region. Which portion of the gene sequence encodes the protein? ​

A)the 5 ¢ untranslated region and the ORF only ​
B)the ORF only
C)the ORF and 3 ¢ untranslated region only
D)the 5 ¢ and 3 ¢ untranslated regions only
E)the ORF, 5 ¢ untranslated region, and 3 ¢ untranslated region

Question 62

Human and chimpanzee genomes share 96% DNA sequence identity. What most likely causes humans to be phenotypically distinct from chimpanzees? ​

A)the presence of many new genes unique to humans
B)a much larger human genome compared to the chimpanzee genome
C)the loss of higher functioning genes in chimpanzees
D)dramatic changes in chromosome structure and organization in humans
E)small mutations in protein coding sequences and changes in regulatory units of human genes

Question 65

Which was the first mammalian genome sequenced?

A)chimpanzee ​
B)gorilla
C)mouse
D)human
E)sheep

Question 67

Genes with novel functions are most commonly produced by ____.

A)inversion of DNA sequences
B)nondisjunction during meiosis
C)unequal crossing-over
D)exon shuffling
E)small mutations

Question 69

A researcher is interested in creating a phylogenetic tree showing the evolutionary relationship of several cyanobacterial species based on the closeness of their nitrogenase gene sequences. Which field of research most directly applies to the researcher's project?

A)comparative proteomics
B)comparative genomics
C)comparative transcriptomics
D)comparative phylogenetics
E)comparative phenotype

Question 72

Chromosomal rearrangement can occur by ____.

A)translocation only
B)inversion only
C)translocation and inversion
D)point mutations
E)alternative splicing

Question 73

Which gene-altering event is most likely to create a new gene encoding a functional protein? ​

A)gene duplication followed by small mutations ​
B)gene duplication followed by large mutations
C)exon shuffling
D)transposition of DNA sequences
E)inversion of DNA sequences

Question 75

Which ethical dilemma may arise from the application of pharmagogenomics? ​

A)The use of embryonic stem cells for gene therapy. ​
B)The discovery of a gene that predicts an unfavorable drug response in an individual, for whom there are no alternative treatments available.
C)The use of vaccination to prevent diseases.
D)The use of blood transfusions to treat diseases.
E)The introduction of foreign genes to restore loss of vital gene function in a patient with an infectious disease.

Question 77

Pharmacogenomics is the study of ____. ​

A)DNA mutations that decrease well-being ​
B)genes that make an organism prone to certain diseases
C)disease resistance genes in an organism's genome
D)the antibiotic resistance genes in an organism's genome
E)the ways in which genes affect an individual's response to drug therapy

Question 79

An application of pharmacogenomics is the study of ____ for determining the appropriate dosages of certain drugs in specific patients. ​

A)drug metabolism genes ​
B)body size
C)blood volume
D)trial and error methods
E)drug interactions