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September 1, 2022
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Chapter
11
– Genome Alterations
– Mutation and Epigenetics
True / False
1.
When the number
of
trinucleotide repeats
in
a gen
e
is
significantly above
normal,
it
can
produce a mutant phenotype.
a.
True
b.
False
True
11
-5 Mutations
at
the Molecular Level:
DNA
as
a Target
expansion.
2.
Nonsense mutations change termination
codons into amino acid codon
s.
a.
True
b.
False
False
11
-5 Mutations
at
the Molecular Level:
DNA
as
a Target
3.
PBDEs have
not
been linked directly
to
cancer
in
test animal
s.
a.
True
b.
False
True
11
-1 Are Some Flame Retardants Dangerou
s?
4.
Halogen-containing organic compo
unds persist
in
the environment for
approximately five years.
a.
True
b.
False
False
11
-1 Are Some Flame Retardants Dangerou
s?
5.
A mutation
of
an
autosomal recessive trait
can
remain undetected fo
r generations.
a.
True
b.
False
True
11
-3 Detecting Mutations and Measuring
Mutation Rates
6.
Mutations
in
germ cells are passed
on
only
to
other germ cells
in
members
of
future generations.
a.
True
b.
False
False
11
-2 Mutations Are Heritable Changes
in
DNA
7.
Most often, radiation doses are expressed
in
terms
of
damage.
a.
True
b.
False
True
11
-4 Mutations Can
Be
Spontaneous
or
Induced
8.
Control systems
in
the cell
can
indu
ce cell suicide,
or
apoptosis,
in
cells with excessive
DNA
damage.
a.
True
b.
False
True
11
-6 Mutations Can
Be
Repaired
9.
People with cystic fibrosis display a sing
le phenotype for the disorder.
a.
True
b.
False
False
11
-7 Mutations, Genotypes, and Phenotypes
phenotypes.
10.
Beckwith-Wiedemann syndrome
is
a cell growth disorder that causes enlarge
d organs, high birth weight,
and
predisposition
to
cancer.
a.
True
b.
False
11
-8 Epigenetic Changes Involve
Reversible Alterations
to
the
Genome
Chapter
11
– Genome Alterations
– Mutation and Epigenetics
Multiple Choice
11.
New
____ mutations
can
often
be
detected
by
examining the inheritance
of
the trait
in
males.
a.
mitochondrial
b.
imprinting
c.
autosomal dominant
d.
autosomal recessive
e.
X-linked
e
Bloom’s: Understand
11
-3 Detecting Mutations and Measuring
Mutation Rates
rates and list factors affecting
those rates.
12.
Mutation rates
of
human genes are expressed
as
the number
of
____.
a.
nucleotides substitutions per gene
b.
frameshift mutations per
genome
c.
mutated alleles per genome
d.
induced mutations per generation
e.
mutated alleles per gene
in
each
generation
e
Bloom’s: Understand
11
-3 Detecting Mutations and Measuring
Mutation Rates
rates and list factors affecting
those rates.
13.
What
is
the largest single source
of
radiation
exposure for the average person
in
the U.S.?
a.
radon
b.
medical X-rays
c.
cosmic
d.
nuclear medicine
e.
consumer products
a
Bloom’s: Remember
11
-4 Mutations Can
Be
Spontaneous
or
Induced
mutations associated with
each
cause.
14.
What occurs
in
a missense mutation?
a.
All
of
the amino acids beyond the
mutation point are changed.
b.
A nucleotide
is
added
to
the
DNA.
c.
A nucleotide
is
deleted from the
DNA.
Beckwith-Wiedemann syndrome
as
an
example.
Chapter
11
– Genome Alterations
– Mutation and Epigenetics
d.
A single amino acid
is
substituted
for another
in
a protein.
e.
The protein
is
always completely no
nfunctional.
d
Bloom’s: Understand
11
-5 Mutations
at
the Molecular Level:
DNA
as
a Target
and describe the different types
and possible consequences
of
each.
15.
Mutagenic chemicals that ____
and are incorporated into
DNA
or
RNA
du
ring synthesis are called base analogs.
a.
resemble nucleotides
b.
resemble genes
c.
resemble amino acids
d.
cause deletion mutations
e.
cause frameshift mutations
a
Bloom’s: Understand
11
-4 Mutations Can
Be
Spontaneous
or
Induced
mutations associated with
each
cause.
16.
If
a genetic disorder appears
in
a family with
no
prior history, and
is
fully
expressed
by
everyone carrying that allele,
it
is
most likely a(n) ____ trait.
a.
autosomal dominant
b.
autosomal recessive
c.
X-linked recessive
d.
Y-linked
e.
mitochondrial
a
Bloom’s: Understand
11
-3 Detecting Mutations and Measuring
Mutation Rates
source
of
an
autosomal recessive mutatio
n.
17.
When ____
is
incorporated into
DNA
or
RNA
durin
g synthesis,
it
will create a(n) __
__.
a.
carbon; base analog
b.
oxygen; base analog
c.
5-bromouracil; nucleotid
e substitution mutation
d.
5-bromouracil; frameshift mutatio
n
e.
oxygen; nucleotide substitutio
n mutation
c
Bloom’s: Understand
mutations associated with
each
cause.
18.
PBDEs are
____.
a.
permitted
in
many European
countries
but
banned
in
the United States
b.
permitted
in
only
one
European country
and
in
only
11
states
in
the United States
c.
banned worldwide
but
are still being
used illegally
d.
banned
in
many European count
ries
but
permitted
in
most states
in
the United
States
e.
banned
in
many Europeans cou
ntries and all states
in
the United
States
d
Bloom’s: Remember
11
-1 Are Some Flame Retardants Dangerou
s?
possible negative health effects
on
humans
and other animals.
19.
Several lines
of
research provide strong evid
ence that ____
to
environmental signals influence
behavior.
a.
epigenetic responses
b.
epigenetic feedback
c.
base analog reconstruction
due
d.
base analog reactions
e.
base analog responses
Bloom’s: Understand
11
-8 Epigenetic Changes Involve
Reversible Alterations
to
the
Genome
20.
Genetic imprinting
is
caused
by
____.
a.
insertion
of
a nucleotide into
an
exon
b.
deletion
of
an
amino acid from the mRNA
strand
c.
a frameshift mutation
d.
epigenetic changes
to
DNA
e.
a change
in
a termination codon
d
Bloom’s: Understand
11
-8 Epigenetic Changes Involve
Reversible Alterations
to
the
Genome
phenotypic expression.
21.
Mutations are changes
in
the nucleotide sequence
of
DNA
that
____.
a.
do
not occur
in
the germ
cells
b.
do
not occur
in
the somatic cells
c.
are always chemically induced
d.
are always spontaneous
e.
can
be
passed
on
to
daughter cells
Bloom’s: Understand
22.
As
radiation strikes molecules
in
cells,
it
creates
____.
a.
charged atoms called isotopes
b.
charged atoms called ions
c.
excess storage
of
tRNA
d.
excess copies
of
mRNA
e.
excess
DNA
polymerase
b
Bloom’s: Understand
11
-4 Mutations Can
Be
Spontaneous
or
Induced
mutations associated with
each
cause.
23.
As
DNA
polymerase synthesizes a
new
DNA
strand,
it
can
____.
a.
detect
an
incorrect nucleotide
b.
not
detect
an
incorrect nucleotide
c.
induce apoptosis when
it
detects a mist
ake
in
DNA
synthesis
d.
induce senescence when
it
detects a
mistake
in
DNA
synthesis
e.
immediately stop the cell cycle
Bloom’s: Understand
11
-6 Mutations Can
Be
Repaired
24.
Several genetic disorders, including Fanconi
anemia and ataxia telangiectasia, are caus
ed
by
mutations
in
____.
a.
the cell wall
b.
mitochondrial
DNA
c.
ribosome structure
d.
DNA
repair genes
e.
DNA
polymerase genes
d
Bloom’s: Understand
11
-6 Mutations Can
Be
Repaired
25.
In
sickle cell anemia, affected individuals carry
____.
a.
one
of
several different nucleotide substitutions
b.
the same single nucleotide sub
stitution
c.
more than one nucleotide substitu
tion
11
-2 Mutations Are Heritable Changes
in
DNA
Chapter
11
– Genome Alterations
– Mutation and Epigenetics
d.
a number
of
mutant alleles
e.
one
mutant allele
in
several genes
b
Bloom’s: Understand
11
-7 Mutations, Genotypes, and Phenotypes
ph
enotypes.
26.
Identical twins have identical
____,
but they
do
not always have identical ____.
a.
mitochondrial
DNA;
genot
ypes
b.
genotypes; mitochondrial
DNA
c.
genotypes; phenotypes
d.
phenotypes; genotypes
e.
phenotypes; mitochondrial
DNA
Bloom’s: Understand
11
-8 Epigenetic Changes Involve
Reversible Alterations
to
the
Genome
epigenetic modifications and
mutations.
27.
A promoter
is
a regulatory regio
n located
at
the
____.
a.
beginning
of
a gene
b.
end
of
a gene
c.
beginning
of
a chromosome
d.
centromere
of
a chromosome
e.
end
of
a chromosome
Bloom’s: Understand
11
-8 Epigenetic Changes Involve
Reversible Alterations
to
the
Genome
epigenetic modifications and
mutations.
28.
Because there
was
no
previous history
of
hemophilia
in
Queen
Victoria’s
family, and
because she transmitted the
mutant allele
to
a number
of
her children,
it
is
reasonable
to
assume th
at ____.
a.
her father was homozygous fo
r the disorder
b.
her mother
was
homozygous for
the disorder
c.
her sister was a heterozygous carrier
d.
she
was
homozygous
for the disorder
e.
she
was
a heterozygous
carrier
Bloom’s: Understand
determine the origin
of
an
abnormal ph
enotype, and explain
why
it
is
difficult
to
identify
the
29.
Frameshift mutations change the number
of
____
in
the gene
and usually cause large-scale changes
in
th
e
____
sequence
of
the protein.
a.
polypeptides; nucleotide
b.
amino acids; allelic
c.
alleles; amino acid
d.
nucleotides; amino acid
e.
amino acids; nucleotide
d
Bloom’s: Understand
11
-5 Mutations
at
the Molecular Level:
DNA
as
a Target
and describe the different types
and possible consequences
of
each.
30.
Sense mutations produce
____.
a.
elongated proteins
b.
shortened proteins
c.
extra termination codons
d.
frameshifts
e.
cell death
a
Bloom’s: Understand
11
-5 Mutations
at
the Molecular Level:
DNA
as
a Target
and describe the different types
and possible consequences
of
each.
Completion
31.
____________________ are mutations invo
lving the increase
of
the number
of
repeat
sequences
in
genes.
Allelic expansions
Bloom’s: Understand
11
-5 Mutations
at
the Molecular Level:
DNA
as
a Target
expansion.
32.
Insertion
or
deletion
of
a nucleotide
in
a gene causes a type
of
mutation
called a(n) ____________________
mutation.
frameshift
Bloom’s: Understand
11
-5 Mutations
at
the Molecular Level:
DNA
as
a Target
and describe the different types
and possible consequences
of
each.
33.
Selective expression
of
either the maternal
or
paternal copy
of
a gene
is
called ____________
________.
genetic imprinting
Bloom’s: Remember
source
of
an
autosomal recessive mutatio
n.
34.
The ability
of
DNA
polymerase
to
repair
its
own nucleotid
e mismatches
is
called __________
__________.
35.
Mutations
in
____________________
cells will
be
passed
on
by
cell division,
but
cannot
be
transmitted
to
fu
ture
generations.
36.
Radiation
in
the environment that contrib
utes
to
radiation exposure
is
called ____
________________ radiation.
37.
A purine
or
pyrimidine that differs
in
chemical structure
from those normally found
in
DNA
or
RNA
is
called a(n)
____________________.
38.
Beckwith-Wiedemann syndrome
results from abnormalities
of
____________________.
39.
The epigenetic state
of
a cell
is
called
its
__________
__________.
40.
In
the 1970s,
children’s
pajamas were treated with
a(n) ____________________
called tris-BP.
41.
Tris
–
BP
was
banned after the discovery
that the chemical caused cancer
in
test animal
s and
was
____________________
through the ____________________
by
those wearing
treated clothing.
42.
The process
by
which electromagnetic energy
travels through space
is
called __
__.
43.
When the direct method
of
measuring mutatio
n rates
is
used, estimates are m
ade for a specific
____________________
over a number
of
____________________.
44.
An
individual with cystic fibrosis
carrying two different mutant alleles would
be
a(n) ____________________
heterozygote for the di
sease.
45.
A form
of
mutation associated with the expansion
in
copy number
of
a nucleotide triplet
in
or
near a gene
is
called
a(n) ____________________.
46.
Indirect methods for measuring
mutation rates make inferences from levels
of
genetic variation between and among
____________________.
47.
Nucleotide substitutions are mutations
that alter the ____________________,
but
not
the ____________________,
of
nucleotides
in
a
DNA
molecule.
48.
A cell that accumulates lots
of
mutational
damage
to
its
DNA
may
escape the
normal controls
of
the cell cycle and
become
___________________
_.
49.
Many
cases
of
epigenetic modification
involve adding a methyl group
to
the
DNA
in
promoters, a process called
____________________.
50.
Individuals with ____________________
are extremely sensitive
to
sun
light and develop skin cancer
at
a rate
1000
times above normal.
Chapter
11
– Genome Alterations
– Mutation and Epigenetics
Essay
51.
Explain why individuals with cystic fibro
sis have different levels
of
severity
of
the disease.
52.
Explain how, when improper base pairi
ng escapes repair
by
the proofreading
system, cells are able
to
detect and repa
ir
mutations.
53.
Summarize some factors known
to
influence mutation rates
of
genes.
54.
Discuss
how
geneticists have concluded that th
e X-linked form
of
hemophilia that spread
through the royal families
of
Western Europe and Russia
in
the nineteenth and twentieth centuries prob
ably originated with Queen Victoria.
55.
Explain what might occur when pu
rine
or
pyrimidine bases
in
nucleotides undergo
tautomeric shifts.
11
-4 Mutations Can
Be
Spontaneous
or
Induced
56.
Summarize the arguments both
for and against irradiating foods.
11
-4 Mutations Can
Be
Spontaneous
or
Induced
57.
Explain why a frameshift mutation
can
have such devastating effects.
11
-5 Mutations
at
the Molecular Level:
DNA
as
a Target
58.
Distinguish between sense and nonsense mutations
and describe the characteristics
of
a protein
affected
by
each
type
of
mutation.
Chapter
11
– Genome Alterations
– Mutation and Epigenetics
59.
Describe
how
an
epigenetic trait differs from a mutated trait.
60.
Summarize research conducted
in
order
to
identify
how
epigenetic changes
might affect the risks
of
depression
and
suicide
in
certain individuals. Comment
on
the limitations
of
this study.