Mutation Flashcards

(66 cards)

1
Q

is a change in a DNA sequence that often contributes to diversity among organisms

A

mutation

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2
Q

Mutations can result from DNA copying mistakes made during (4)

A

cell division
exposure to ionizing radiation
exposure to mutagens
infection by viruses

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3
Q

is the process of altering a DNA sequence that range from a single base, to deletion or duplication of ten, hundreds or even millions of bases, to missing or addition of entire chromosomes.

A

mutation

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4
Q

Genes and chromosomes can mutate in somatic tissue

A

somatic mutations

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5
Q

Genes and chromosomes can mutate in either germinal tissue

A

germinal mutation

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6
Q

the change occurs during the DNA replication that precedes meiosis

A

germline mutation

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7
Q

The resulting gamete and all the cells that descend from it after fertilization have the mutation—that is, every cell in the body.

A

germline mutation

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8
Q

happens during DNA replication before a mitotic cell division

A

somatic mutation

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9
Q

are more likely to occur in cells that divide often, such as hair root cells, because there are more opportunities for replication errors.

A

somatic mutations

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10
Q

Somatic mutations are more likely to occur in cells that divide often, such as __ ___ cells, because there are more opportunities for replication errors.

A

hair root

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11
Q

Mutagenesis may occur (2)

A

spontaneously
induced

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12
Q

can happens naturally during normal cellular processes.

A

spontaneous mutation

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13
Q

A spontaneous mutation may be due to a mistake during

A

DNA replication

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14
Q

A mutation caused by an environmental factor, or mutagen, is known as an

A

induced mutation

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15
Q

typical mutagens include

A

chemicals
radiation

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16
Q

chemical mutagens

A

nitrous acid
formaldehyde
ethylethane
sulphonate

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17
Q

radiation mutagens example

A

X-rays
UV light
nuclear radiation (physical mutagens)

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18
Q

may cause bonding between the adjacent nucleotides on one strand of DNA molecule.

A

UV radiation

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19
Q

this prohibits normal bonding between complementary nucleotides of the opposing strand. This causes a bulge in the DNA double helix.

A

bonding between adjacent nucleotides due to UV radiation

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20
Q

is a change in a single nucleotide in DNA.

A

gene mutations

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21
Q

It is usually less deleterious than chromosomal aberrations.

A

gene mutation

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22
Q

a purine replaces a pyrimidine, or vice versa;

A

transversion

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23
Q

a purine replaces a purine or a pyrimidine replaces a pyrimidine.

A

transition

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24
Q

gene mutation include what kind of mutation

A

same/silent
missense
nonsense mutation

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25
Mutated codon codes for the same amino acid.
silent/same sense mutation
26
effect of silent/same sense mutation
none
27
Mutated codon codes for a different amino acid.
missense mutation
28
missense mutation effect
variable
29
Mutated codon is a premature stop codon.
nonsense mutation
30
effect of nonsense mutation
serious
31
is a deletion or insertion of one or more nucleotides that changes the reading frame of the base sequence
frameshift mutation
32
remove nucleotides
deletions
33
adds nucleotides
insertions
34
are changes involving chromosome structure or number.
chromosomal mutations
35
There are three general types of chromosomal mutation
changes in number of whole chromosome change involving addition or subtraction of one or more chromosomes structural changes involving parts of chromosomes
36
changes in the number of the whole chromosomes set (genome) or
euploidy
37
changes involving addition or subtraction of one or more chromosomes
aneuploidy
38
x type of euploidy
monoploid
39
type of euploidy 2x
diploid
40
type of euploidy 3x
triploid
41
type of euploidy 4x
tetraploid
42
type of euploidy 6x
hexaploid
43
type of euploidy 8x
octaploid
44
involves addition or missing of the whole chromosome.
aneuploidy
45
2n+1
trisomy
46
trisomy 21
down syndrome
47
trisomy 13
patau's syndrome
48
trisomy 18
Edward's syndrome
49
XXY
Klinefelter syndrome
50
XXX
triplo X syndrome
51
XYY
double Y sondrome
52
2n+2
tetrasomy
53
2n+2 chrom 8
tetrasomy 18
54
2n-1
monosomy
55
X
turner's syndrome
56
can come about due to deletions or deficiency, duplications, and rearrangements of chromosome segments.
changes in chromosome structure
57
Deletion of chromosome 22 long arm
philadelphia 22
58
Deletion of chromosome 5 short arm
cri du chat syndrome
59
Deletion of chromosome X short arm
muscular dystrophy
60
Duplication of 17p12
charcot marie tooth disease type I
61
Inversion of chromosome 9
chromosome 9 inversion
62
Involves chromosomes 13, 14, 15, 21 & 22 translocation
roberstonian translocation
63
inversions do not include the centromere
paracentric
64
pericentric
Involves a segment of DNA that spans the centromere, including both chromosome arms (short and long arms). Breaks occur on both sides of the centromere
65
two non-homologous chromosomes exchange segments, essentially swapping pieces of genetic material.
reciprocal translocation
66
involves the fusion of the long arms of two acrocentric chromosomes (chromosomes 13, 14, 15, 21, or 22) at their centromeres, resulting in one chromosome with the combined genetic material and the short arms of the fused chromosomes being los
roberstonian translation