1. The
collection of proteins that can be
produced by a given species is:
A)
Considered that species' genetic complement.
B)
Correlated with the size of the organism.
D) All
of these.
E) None
of these
2. A
cDNA library:
A) Can also be called an expressed
sequence tag (EST) library.
B) Consists
of coding sequences from genes that are expressed.
C) Is
specific to the set of conditions under which the original mRNA was generated.
E) None
of these.
3. The
technique of subtractive hybridization allows identification of genes that are
selectively activated under a certain set of conditions.
B) False
4. Which of these questions could be
answered using subtractive hybridization?
A) What genes are required for basic
cellular functions?
B) What site is bound by a kidney
specific transcription factor?
D) All of these
E)
None of these
5. A single microarray may have a
surface area of less than three square inches, yet may contain unique spots of
tens of thousands of gene sequences.
B) False
6.
Which of these might be an advantage to genetic testing
of individuals via microarrays?
A) Many
different potential mutations in a single gene could be tested at once.
B)
Expression patterns of many different genes can be
analyzed simultaneously.
C)
Microarray analysis can provide information on relative
levels of expression of particular genes.
E)
None of these
7.
Which of these would not be a valid reason that use of
microarray technology to differentiate between closely related bacterial
species and subspecies is important?
A)
Certain strains of bacteria are more pathogenic than
other related strains.
B)
Some strains of bacteria are more active in
bioremediation than other related strains.
C)
Infection by different strains of bacteria may require
different therapeutic approaches.
D)
In many cases, critical information about
characteristics of a bacterium causing an infection needs to be immediately
available.
E)
All of the above are valid reasons.
8.
A cluster analysis is the study of groups of genes that
seem to be regulated together.
B)
False
9. The two most common processes that lead to production of
multiple functional proteins from the same DNA sequence are:
A)
RNA editing and alternative splicing.
B)
Protein folding and posttranslational covalent
modifications.
D)
Posttranslational covalent modification and
transcriptional regulation.
E)
RNA editing and base modification.
10. Examples
of irreversible posttranslational covalent modification include acetylation and
phosphorylation.
A)
True
11. Which
of the following statements regarding the proteome is the most correct?
A)
A large proportion of the proteome is expressed by each
cell of a species.
B)
Levels of gene expression at the mRNA level generally
correlate highly with levels of functional protein.
D)
All of the above.
E)
None of the above.
12. In two dimensional gel electrophoresis:
A)
Different forms of the same protein will tend to
migrate at the same position.
B)
Up to about a hundred different proteins can be
distinguished from each other.
C)
Proteins with similar functions will be located near
each other.
D)
All of these.
13. Western
blotting of 2D gel electrophoresis would be a high resolution method of
demonstrating a change in a particular protein as a result of mutation.
B)
False
14. Which
of these conclusions might be drawn from the results of a 2D gel
electrophoresis experiment?
A)
Levels of mRNA expression for two different genes are
lower under one set of conditions than another.
B)
In a mutant cell, the lack of protein expression is due
to production of unstable mRNA, which is rapidly degraded.
C)
A mutation prevents proper posttranslational modification
of a protein.
D)
All of these are reasonable conclusions.
15. Tandem
mass spectrometry can be used to determine the specific amino acid sequence of
a protein
A)
True
- If computers were not able to access the entire genomic sequence of an organism, which of the following techniques might allow determination of the gene sequence that encodes a particular protein?
A) PCR amplification of related gene
sequences.
C) Production of synthetic peptides.
D) All of these.
E) None of these.
- Which of these concerns would apply to functional protein microarrays but not antibody microarrays?
A) Antibodies recognize relatively short
peptide sequences from a protein, and presence of the same peptide sequence in
several proteins is possible.
B) Three dimensional structure of a
protein is essential for correct function, and the process of microarray
preparation may interfere with this structure.
C) Certain functions, such as structural
support of a cell, may not be amenable to analysis on a microarray.
D) All of these apply to functional
protein microarrays but not antibody microarrays.
E) All of these apply equally to both
types of microarrays.
- Functional protein microarrays can identify protein functions only if their sequence is known.
A) True
- Which of the following pieces of information would not be required for a computer program to determine exon/intron structure of a gene?
A) A table correlating codons to amino
acids.
C) Splice site signals for the species
under study.
D) All of these pieces of information
would be requireD. E. None of these pieces of information would be requireD.
This would be a required piece of information; at least the start and stop
codons must be recognized by the computer program to identify potential open
reading frames.
- How many potential open reading frames are present in a DNA sequence?
A) One
B) Three
D) More
than Six
E) None
of these
- A computer program must be written in a specific language in order for the computer to understand what needs to be done.
B) False
- You have cloned a new gene from your favorite species of experimental organism, which has had very few genes cloned so far. Which of the following techniques would you expect to provide information about the function of this gene?
A) Comparison of regulatory sequences to
other DNA sequences in this organism.
B) Comparison of regulatory sequences to
DNA sequences from other organisms.
C) Comparison of the gene sequence to other
DNA sequences in this organism.
E) None of these.
- Why might you want to search a database for a protein motif?
A) A specific motif may impart a specific
function to the molecule. You could then identify groups of proteins that may have
similar functions.
B) Presence of a specific motif in several
proteins indicates that they are likely to be all from the same species.
C) Absence of a specific motif from one of
a pair of otherwise similar proteins indicates that they are produced by
alternative splicing of the same gene.
D) All of the above.
E) None of the above.
- Which of these would not be an example of sequence element?
A) A recognition site for binding of a
particular transcription factor.
B) A restriction endonuclease cut site.
D) A stop codon.
E) None of these.
- In an analysis of eukaryotic gene, you identify several nonoverlapping open reading frames, but they are not all in the same frame. Which explanation makes the most sense?
A) By random chance, a second reading
frame within the gene also has an open reading frame.
C) This is a mutant allele that has had
several small insertions.
D) All of these.
E) None of these.
- Identification of a gene that does not fit the typical patterns for eukaryotic gene structure would not have a dramatic effect on bioinformatics.
A) True
- Homologous genes:
B) Would be expected to be more similar in
distantly related organisms than in organisms that are closely related.
C) May have become similar to each other
by random mutation.
D) All of these.
E) None of these.
- A multiple sequence alignment of related genes can identify amino acids required for protein function.
B) False
- You clone a novel gene from your favorite experimental organism, and identify the sequence of the gene itself and the protein. You would like to know if this gene is regulated by any known transcription factors. Which technique would be best suited to provide you evidence to address this question?
A) BLAST analysis of the protein sequence.
B) BLAST analysis of the DNA from the
coding sequence.
C) BLAST analysis of the DNA from the
upstream regions.
- Secondary structure of RNA molecules:
B) Is generated by covalent bonding
between sections of the RNA molecule.
C) Can be described as interactions
between portions of the backbone of the molecule.
D) Does not have an impact on function of
the molecule.
Source: http://mcgraw-hill.com
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