exam 5 Flashcards

1
Q

blending hypothesis

A

the idea that genetic material contributed by the two parents mixes in a manner analogous to the way blue and yellow paints blend to make green

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2
Q

particulate hypothesis

A

gene idea

parents pass on discrete heritable units, genes, that retain their separate identities in offspring

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3
Q

character

A

heritable feature that varies among individuals

ex. flower color

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4
Q

trait

A

each variant for a character

ex. purple or white flowers?

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5
Q

true breeding

A

over many generations of self pollination had produced only the same variety as the parent plant
homozygous dominant or recessive

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6
Q

hybridization

A

crossing of two true breeding varieties

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7
Q

P generation

A

parental generation

two true breeding parents

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8
Q

F1 generation

A

first filial generation

hybrid offspring of P generation

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9
Q

F2 generation

A

second filial generation

result of self pollination of F1 generation

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10
Q

alleles

A

alternate versions of a gene

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11
Q

dominant allele

A

determines the organism’s appearance

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12
Q

recessive allele

A

no noticable effect on the organisms appearence except in the absence of a dominant allele

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13
Q

law of segregation

A

the two alleles for a heritable character segregate (separate from each other) during gamete formation and end up in different gametes

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14
Q

Punnett Square

A

handy diagrammatic device for predicting the allele composition of all ofspring resulting from a cross between individuals of known genetic makeup

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15
Q

homozygous

A

pair of identical alleles

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16
Q

heterozygous

A

two different alleles for its gene

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17
Q

phenotype

A

appearance or observable traits

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18
Q

genotype

A

genetic makeup

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19
Q

testcross <!>

A

breeding an organism of unknown genotype with a recessive homozygote
depending on the phenotypes of the offspring you can tell the genotype of the parent (4:0 ratio means homozygous dominant and 3:1 ratio means heterozygous)

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20
Q

monohybrids

A

they were heterozygous for the one particular character being followed in the cross

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21
Q

monohybrid cross

A

cross between two heterozygotes

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22
Q

dihybrids

A

individuals heterozygous for two characters being followed in the cross

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23
Q

dihybrid cross

A

a cross between F1 dihybrids (heterozygotes)

always yields a 9;3;3;1 phenotypic ratio

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24
Q

law of independent assortment

A

two or more genes assort independently, that is, each pair of alleles segregates independently of each other pari during gamete formation
aka FOIL

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25
multiplication rule
multiply the probability of one event by the probability of another
26
addition rule
the probability that any one of two or more mutually exclusive events will occur is calculated by adding their individual probabilities
27
complete dominance
mendelian genetics | dominant allele has complete dominance and is the only one shown over the recessive allele
28
incomplete dominance
blended intermidiate not completely dominant white+red=pink
29
codominance
two alleles each affect the phenotype in separate distinguishable ways black spots on a white chicken
30
Tay-Sachs disease
an inherited disorder in humans the brain cells of a child with this cannot metabolize certain lipids because a crucial enzyme does not work properly as these lipids accumulate in brain cells, the child begins to suffer seizures, blindness and degeneration of motor and mental performance and dies within a few years
31
pleiotropy
genes that have multiple phenotypic effects | one gene codes for more than one thing
32
epistasis
a gene at one locus alters that of a gene at a second locus | labradors (217)
33
quantitative characters
characters vary in the population in gradations along a continuum skin color
34
polygenic inheritance
quantitative variation usually indicates polygenic inheritance, the additive effect of two or more genes on a single phenotypic character reverse pleiotropy: many genes code for one phenotype
35
multifactorial
many factors, both genetic and environmental, collectively influence phenotype
36
pedigree
geneticists assemble information about members of a family into a tree diagram that describes the traits of parents and children across the generations
37
square/circle
square is male | circle is female
38
carriers
heterozygotes may transmit the recessive allele to their offspring and thus are called carriers
39
cystic fibrosis
common lethal genetic disease in the united states most common in european descent (4% carriers) the normal allele for this gene codes for a membrane protein that functions in the transport of chloride ions between certain cells and the extracellular fluid. these chloride channels are defective or absent in the plasma membrane of children who inherit two recessive alleles for cystic fibrosis
40
sickle cell disease
most common inherited disorder among people of african descent 1/400 african americans caused by the substitution of a single amino acid in the hemoglobi protein of red blood cells; in homozygous individuals, all hemoglobin is of the sickle cell variety
41
anchondroplasia
form of dwarfism that occurs in one of every 25,000 people | dominant allele
42
huntington's disease
degenerative disease of the nervous system, caused by a lethal dominant allele that has no obvious phenotypic effect until the individual is about 35-45 years old. once the deterioration of the nervous system begins, it is irreversible and inevitably fatal
43
chromosome theory of inheritance
mendelian genes have specific loci along chromosomes, and it is the chromosomes that undergo segregation and independent assortment
44
Thomas Hunt Morgan
experimental embryologist | used Drosophila Melanogaster to do experiments on sex linked genes
45
Drosophila melanogaster | qualities making them good for experimentation
prolific breeders: single mating will produce hundreds of offspring and a new generation can be bred every 2 weeks only 4 pairs of chromosomes which are easily distinguishable under a light microscope
46
wild type
the phenotype for a character most commonly observed in natural populations (w+)
47
mutant type
traits that are alternatives to the wild type they are due to alleles assumed to have originated as changes, or mutations in the wild type allele (w)
48
XX
female
49
XY
male
50
sex-linked gene
a gene located on either sex chromosome those on Y: Y-linked genes those on X: X-linked genes
51
hemizygous
used for describing traits in males since they only have one possibility for an allele
52
duchenne muscular dystrophy
affects about 1 in every 3500 males born in the US disease is characterized by a progressive weakening of the muscles and loss of coordination rarely live past their 20s
53
hemophilia
x-linked recessive disorder absences of one or more of the proteins required for blood clotting when a person with hemophilia is injured bleeding is prolonged because a firm cut is slow to form
54
Barr body
inactive condensed X chromosome most barr body genes are not expressed barr body chromosomes are activated in the ovaries
55
linked genes
genes located near each other on the same chromosome tend to be inherited together in genetic crosses
56
genetic recombination
result from crossing over | the production of offspring with combinations of traits that differ from those found in either P generation parent
57
parental ypes
offspring that inherit the phenotype that matches eithe of the parental (P) generation phenotypes
58
recombinant types
nonparental phenotypes that do not reseble either parent
59
crossing over
accounts for the recombination of linked genes in crossing over, which occurs while replicated homologous chromsomes are paired during prophase of meiosis I, a set of proteins orchestrates an exchange of corresponding segments of one maternal and one parental chromatid
60
genetic map
Alfred H. Sturtevant | an ordered list of the genetic loci along a particular chromosome
61
recombination frequency
percentage of recombinant offspring
62
linkage map
genetic map based on recombination frequencies
63
map units
one map unit is equivalent to 1% recombination frequency | centimorgan
64
nondisjunction
members of a pair of homologous chromosomes don't move apart properly during meiosis ! or sister chromatids fail to separate during meiosis ii
65
aneuploidy
if either of the aberrant gametes unites with a normal one at fertilization, the zygote will also have an abnormal number of a particular chromosome
66
monosomic
fertilization involving a gamete that has no copy of a particular chromosome will lead to a missing chromosome in the zygote 2n-1
67
trisomic
if a chromosome present in triplicate in the zygote | 2n+1
68
polyploidy
plants 3n 4n
69
deletion
chromosomal fragment is lost
70
duplication
repeats a chromosomal segment
71
inversion
a chromosomal fragment reattaches to the origninal chromosome but in the reverse orientation
72
translocation
fragment joins a nonhomologous chromsome switch occurs reciprocal mostly
73
down syndrome
trisomy 21 one additional chromosome 21 disorder
74
klinefelter syndrome
XXY | 1/500-1000 live male births
75
trisomy x
XXX
76
Turner syndrome
X0
77
cri du chat
cry of the cat deletion of chromosome 5 baby cries like cat dies