Exam 2 Flashcards

(111 cards)

1
Q

when does crossing over occur

A

prophase 1

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2
Q

what happens in meiosis 2 with normally-linked genes

A

they assort independently and end up in different gametes

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3
Q

what happens if there is no crossing over in meiosis 1

A

there will be no recombinant gametes…they will all be parental

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4
Q

single crossover

A

50% parental, 50% recombinant

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5
Q

recombination frequency equation

A

number of recombinant progeny/all progeny x 100

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6
Q

% recombination white eyes yellow bodies

A

1.5%

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7
Q

% recombination yellow bodies cut wings

A

17.7%

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8
Q

% recombination yellow bodies vermillion eyes

A

34.5%

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9
Q

what is a test cross

A

crossing an F1 with a homozygous recessive

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10
Q

is there recombination in male drosophila

A

no

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11
Q

why do male drosophila not have recombination

A

they don’t form synaptonemal complexes

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12
Q

what is responsible for breakage of chromosomes during crossing over

A

something-ase. protease?

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13
Q

can sister chromatids have crossover

A

they can but wouldn’t do anything?

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14
Q

double crossover - 2 strands

A

2 crossovers occurring, all parental chromosomes

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15
Q

triple crossover

A

three crossovers occurring on the four strands

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16
Q

quadruple crossover

A
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17
Q

double crossover - 3 strands

A

half parental, half recombinant

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18
Q

double crossover - 4 strands

A

all recombinant

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19
Q

% recombination white eyes mini wings

A

31.5%

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20
Q

% recombination yellow body rudimentary wings

A

50%

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21
Q

explain theoretical vs empirical map distances

A

theoretical map distance for percent recombination is always higher than empirical

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22
Q

over what distance is percent recombination a good estimate

A

short distances: less than 25 MU

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23
Q

over what distance is percent recombination a bad estimate

A

long distances: over 35 MU

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24
Q

are far apart genes likely to be linked?

A

no

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25
how can you find the number of recombinant offspring in a cross
divide recombinant by 2 and excess by two and multiply proportion by whole number of progeny to get estimate.
26
calculating recombinant percent from first gene to middle gene
R1 + R1 + D + D / total # x 100
27
calculating recombinant percent from middle gene to end gene
R2 + R2 + D + D / total # x 100
28
do you do count doubles twice when calculating recombination frequency
yes
29
calculating coefficient of coincidence
number of doubles obs / number of doubles exp
30
calculating interference
1-coefficient of coincidence
31
probability of a crossover in region 1
.122
32
probability of a crossover in region 2
.146
33
probability of a double crossover
.018
34
how do you calculate the number of expected doubles
you multiply .018 by the total number of progeny
35
what if interference is 1
no doubles occured
36
what if interference is negative
more occurred than expected
37
are genetic maps linear
yes
38
are map distances additive
yes
39
characteristics of 3 unlinked genes
all phenotypic classes will be equal in frequency
40
characteristics of 2 linked, 1 unlinked genes
parentals=doubles, 2 sets of recombinants = but less than parentals and doubles
41
characteristics of 3 linked genes
four distinct sets of phenotypic classes
42
G and Q banding
fluoresces karyotypes to show chromosome bands
43
what are the 4 chromosome aberrations
deletions, duplications, inversions, translocations
44
what is a chromosome deletion
a portion of the chromosome is deleted. usually recessive lethal. can show a dominant effect.
45
what is a chromosome duplication
a portion of the chromosome is duplicated.
46
what is a chromosome inversion
a portion of the chromosome is flipped 180 degrees
47
what is a chromosome translocation
a portion of the chromosome moves to a non-homologous chromosome or another place on the same chromosome
48
pseudodominance
when a single recessive allele is inherited but still expressed
49
when does the deletion loop form on chromosome deletions
during prophase 1
50
what are polytene chromosomes
they remain condensed during interphase. homologous chromosomes remain paired even though there is no meiosis. they are large and easy to see.
51
genetic vs cytological maps
co-linear but not co-metric
52
cri-du-chat syndrome
cat-like cry, intellectually challenged, small head, small jaw, wide-set eyes
53
deletions are consistently found where
in patients with solid tumors
54
duplications in wild-type chromosomes
chromosomes don't align properly, so unequal crossing over
55
pericentric inversion
includes the centromere
56
paracentric inversion
does not include the centromere
57
inversion characteristics
no gene imbalance, can have position effects, if moved next to heterochromatin position effects can be patchy
58
dna + proteins
chromatin
59
euchromatin
stains normally, thought to contain genes, loosely packed
60
heterochromatin
densely staining, condensed chromatin thought to be genetically inert. mostly repetitive dna, tightly packed
61
constitutive
always on
62
facultative
occurring sometimes
63
result of a crossover inside a paracentric inversion
gametes containing chromatin involved in crossover are non-viable. gametes containing chromatin not involved in crossover are viable.
64
result of a crossover inside a pericentric inversion
gametes containing chromatin involved in crossover are non-viable. gametes containing chromatin not involved in crossover are viable.
65
coadapted gene complex
a group of genetic traits with high fitness when they occur together, but without each other have low fitness
66
reciprocal translocation
no predictable phenotypes, pairing of homozygotes is normal, pairing of heterozygotes will result in a cross shape
67
how chromosomes separate in anaphase 1 - alternate segregation
viable gametes
68
how chromosomes separate in anaphase 1 - adjacent 1 segregation
non-viable gametes
69
how chromosomes separate in anaphase 1 - adjacent 2 segregation (rare)
non-viable gametes
70
5:11 translocation
Cr- du Chat
71
8:14 reciprocal translocation
Burkitt's lymphoma
72
Reciprocal Translocations in Oenothera
ring chromosomes
73
polyploid
any organism with more than 2 sets of chromosomes
74
autopolyploids
have multiple of the species' original sets of chromosomes
75
allopolyploids
contain sets of chromosomes from different species
76
pairing possibilities in tetraploids
two bivalents, one quadrivalent, univalent + trivalent
77
in allopolyploids who is viable
F1 will make non-viable progeny
78
why are hybrids sterile
meiosis is highly unstable
79
Karpechenko's Experiments
there can be a few fertile offspring of hybrids
80
XO
Turner's Syndrome
81
XXX
Trisomic X
82
XXXX
Tetrasomic X
83
XXXXX
Pentasomic X
84
XYY
Jacob's Syndrome
85
XXY
Kleinfelter's Syndome
86
XXYY
Kleinfelter's Syndome double trisomic
87
XXXY
Kleinfelter's Syndome tetrasomic
88
2N
normal
89
2N-1
monosomic
90
2N-1-1
double monosomic
91
2N-2
nullosomic
92
2N+1
trisomic
93
2N+1+1
double trisomic
94
2N+2
tetrasomic
95
Barr Body
condensed, inactivated X chromosome
96
Barr Bodies in X0
0
97
Barr Bodies in XX
1
98
Barr Bodies in XXX
2
99
Barr Bodies in XXXX
3
100
Barr Bodies in XXXXX
4
101
Barr Bodies in XY
0
102
Barr Bodies in XYY
0
103
Barr Bodies in XXY
1
104
Barr Bodies in XXYY
1
105
Barr Bodies in XXXY
2
106
Barr Bodies in XXXXY
3
107
mechanism of x-chromosome inactivation
repressor of inactivation binds to one x chromosome
108
Down Syndrome
trisomic 21
109
Edward Syndrome
trisomic 18
110
Patau Syndrome
trisomic 13
111
Warkany Syndrome
trisomic 8