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19: Eukaryotic Genomes: Organization, Regulation, and Evolution
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Pre-Test
Chapter 19: Eukaryotic Genomes: Organization, Regulation, and Evolution
Pre-Test
Pre-Test
1 .
Histones are _____. (Concept 19.1
)
[
Hint
]
master genes that affect development
groups of genes that respond to environmental changes
proteins around which DNA is coiled
portions of genes that are transcribed
portions of genes that are eliminated by DNA splicing
2 .
Your muscle and skin cells are different because _____. (Concept 19.2
)
[
Hint
]
they contain different sets of genes
they contain different chromosome sets
they contain different operons
different genes are switched on and off in each type of cell
they contain different histones
3 .
DNA methylation is a mechanism used by eukaryotes to _____. (Concept 19.2
)
[
Hint
]
inactivate genes
increase the rate of transcription
terminate transcription
facilitate the binding of DNA to intermediate filaments
cause apoptosis
4 .
In humans, the hormone testosterone enters cells and binds to specific proteins, which in turn bind to specific sites on the cells' DNA. These proteins probably act to _____. (Concept 19.2
)
[
Hint
]
help RNA polymerase transcribe certain genes
alter the pattern of DNA splicing
promote recombination
unwind the DNA so that its genes can be transcribed
cause mutations in the DNA
5 .
It is possible for a cell to make proteins that last for months; hemoglobin in red blood cells is a good example. However, many proteins are not this long-lasting; they may be degraded in days, hours, or even minutes. What is the advantage of short-lived proteins? (Concept 19.2
)
[
Hint
]
Most proteins are used only once.
Most cells have a short life span.
Cells lack the raw materials to make most of the proteins they need.
Long-lasting proteins are likely to make the cell cancerous.
Short-lived proteins enable the cells to control their activities precisely and efficiently.
6 .
Which of the following would be most likely to lead to cancer? (Concept 19.3
)
[
Hint
]
amplification of a proto-oncogene and inactivation of a tumor-suppressor gene
hyperactivity of a proto-oncogene and activation of a tumor-suppressor gene
failure of a proto-oncogene to produce a protein and amplification of a tumor-suppressor gene
failure of both a proto-oncogene and a tumor-suppressor gene to produce proteins
hyperactivity of both a proto-oncogene and a tumor-suppressor gene
7 .
In normal cells, the genes that malfunction in cancer usually _____. (Concept 19.3
)
[
Hint
]
control RNA transcription
are responsible for sex determination
code for enzymes involved in cellular respiration
are not present
regulate cell division
8 .
All your cells contain proto-oncogenes, which can change into cancer-causing genes. Why do cells possess such potential time bombs? (Concept 19.3
)
[
Hint
]
Proto-oncogenes protect cells from infection by cancer-causing viruses.
Proto-oncogenes are genetic junk that has not yet been eliminated by natural selection.
Proto-oncogenes are unavoidable environmental carcinogens.
Cells produce proto-oncogenes as a by-product of mitosis.
Proto-oncogenes are necessary for the normal control of cell growth and division.
9 .
Retrotransposons differ from other transposons in that _____. (Concept 19.4
)
[
Hint
]
retrotransposons have lost the ability to move about a genome
retrotransposons are likely to be the remains of a viral infection
retrotransposons have retained the ability to move about a genome, an ability that has been lost by other transposons
retrotransposons move via an RNA transcript, whereas other transposons do not
only retrotransposons can affect gene expression
10 .
Gene duplication has played a critical role in evolution because it _____. (Concept 19.5
)
[
Hint
]
produces redundant copies of existing genes, which are then free to mutate and adopt new functions
increases the number of pseudogenes in the genome
increases the likelihood of viral infection in cells
increases the amount of DNA in the genome
almost always introduces immediate benefits for the organism
©2005 Pearson Education, Inc., publishing as
Benjamin Cummings