lecture 11- genetics Flashcards

1
Q

what do the law of segregation and the law of independent assortment have in common

A

both contribute to genetic diversity

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2
Q

what is incomplete dominance

A

neither allele is dominant
mix/blend of both homozygous alleles
pink flower = mix of homozygous red and white

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3
Q

what is the notation for incomplete dominance alleles (red pink and white)

A

R^1R^1
R^1R^2
R^2R^2

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4
Q

in incomplete dominance what terms do you use for the middle allele

A

heterozygous

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5
Q

in incomplete dominance what is the genotype ratio compared to the phenotype ratio

A

they are equal
all allele combination will display their phenotype

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6
Q

what is codominance

A

both alleles’ phenotype being expressed
not a mix, are independent

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7
Q

what is the notation for codominance

A

same as incomplete dominance (R^1R^2)

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8
Q

is a gene limited to having only two alleles

A

no (blood type antigens)

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9
Q

how many alleles can an individual have for a specific gene

A

two because theres only two homologous chromosomes for that gene

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10
Q

what are the blood cell antigens

A

I^A - type A
I^B - type B
i - type O

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11
Q

what are all the blood types you can have and their notations

A

type A - I^A I^A or I^A i
type B - I^B I^B or I^B i
type AB (codominant) - I^A I^B
type O - ii

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12
Q

what is epistasis

A

presence of a certain allele in one locus that can mask the expression of alleles in a different locus

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13
Q

is the epistasis gene dominant or recessive

A

recessive ee

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14
Q

how does epistasis work

A

if the epistasic gene is homozygous recessive then it blocks another gene from being expressed

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15
Q

what is pleiotropy

A

a single gene that can affect multiple phenotype

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16
Q

how does pleiotropy work

A

when a gene product is used in different cell types or a signaling functions on various targets it affects multiple organs

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17
Q

what are examples of pleiotropy

A

cystic fibrosis (defective protein found in the plasma membrane): affects lungs, intestines, pancreas, liver, sweat glands
sickle cell anemia (defective protein in red blood cells): symptoms such as heart failure, jaundice and pain

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18
Q

what is polygenic inheritance

A

many genes interacting to affect the expression of one trait (opposite of pleiotropy)

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19
Q

example of polygenic inheritance

A

skin color is controlled by at least three genes

20
Q

what is sex-linked inheritance

A

characteristics inherited on sex chromosomes other than sex related ones (mostly X)

21
Q

what types of genes do sex chromosomes contain

A

sex assigned
control of development of secondary sex characteristics (breasts, voice, etc)
other genes: hemophilia and color blindness

22
Q

are sex chromosomes homologous

A

no but they act as homologous (pair up during meiosis)
have a homologous region (bottom, small)

23
Q

where are sex linked genes

A

on one of the sex chromosomes but not on the other

24
Q

what is a hemizygous allele

A

allele that determines the condition in males because they only have that gene on one sex chromosome

25
what is dosage compensation
mechanism that makes the 2 doses in females (XX) and the one dose in males (XY) equivalent
26
how does dosage compensation work in mammals
inactivation of an X chromosome or part of it creation of a barr body (inactive chromosome)
27
what is the point of dosage compensation
avoiding over expression of X genes in females
28
due to X inactivation what changes in the genetic material
nothing, they all keep the same genetic material
29
what is polyploidy
presence of multiple sets of chromosomes (normal)
30
what is aneuploidy
abnormalities caused by the presence or absence of a single chromosome (only affects one chromosome type)
31
what is a nondisjunction
chromosomes failing to separate during meiotic division
32
what is the result of nondisjunction
aneuploidies
33
what is disomy
a normal pair of chromosomes
34
what is trisomy
having an extra chromosome in a pair (3)
35
what is monosomy
missing a chromosome in a pair (1)
36
where can aneuploidies happen
autosomes and sex chromosomes
37
what is the reason for down syndrome
trisomy 21 (extra chromosome #21) so 47 chromosomes instead of 46
38
what are the four chromosome structure mutation
deletion duplication inversion reciprocal translocation (different chromosomes exchanging genes)
39
is a phenotype solely based on genes and why
no its also based on the environment (height = how much you eat, sleep, etc)
40
what are the different types of abnormal sex chromosome numbers
XXX XXY XYY X0 Y0
41
how will a XXX person develop
female mild disorders only one X active taller than average normal sexual development
42
how will a XXY person develop
male have some female characteristics
43
how will a XYY person develop
male normal sexual development taller than average
44
how will a X0 person develop
female underdeveloped ovaries male characteristics (lack breasts)
45
how will a Y0 person develop
death humans cannot live without at least one X chromosome