Mendel and the Gene Idea: Chp 14 Flashcards

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1
Q

p generation

A

true-breeding parents in a genetic cross

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2
Q

f1 generation

A

p generation offspring

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3
Q

f2 generation

A

f1 generation offspring

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4
Q

four concepts explaining mendel’s 3:1 inheritance pattern

A

1: alternative versions of genes cause variations in inherited characteristics among offspring
2: for each character, every organism inherits one allele from each parent
3: if the two alleles are different, then the dominant allele will be fully expressed
4: the two alleles for each character separate during gamete production

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5
Q

mendels law of segragation

A

states that allele pairs separate or segregate during gamete formation, and randomly unite at fertilization

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6
Q

mendels law of independent assortment

A

states that each pair of alleles will segregate independently during gamete formation

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7
Q

homozygous

A

two of the same alleles

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8
Q

heterozygous

A

two different alleles

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9
Q

phenotype

A

refers to an organisms expressed physical traits

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10
Q

genotype

A

refers to an organisms genetic makeup

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11
Q

testcross

A

is done to determine if an individual showing a dominant trait is homozygous or heterozygous

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12
Q

monohybrid cross

A

a cross involving the study of only one character

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13
Q

dihybrid cross

A

a cross intended to study two characters

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14
Q

the rule of multiplication

A

when calculating the probability that two or more independent events will occur together in a specific combination, multiply the probabilities of each of the two events

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15
Q

the rule of addition

A

when calculating the probability that any of two or more mutually exclusive events will occur, you need to addd together their individual probabilities

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16
Q

complete dominance

A

dominance in which the heterozygote and the homozygote for the dominant allele are indistinguishable

17
Q

co dominance

A

occurs when two alleles are dominant and affect the phenotype in two different but equal ways

18
Q

incomplete dominance

A

a type of dominance in which the F1 hybrids have an appearance that is in between that of the two parents

19
Q

multiple alleles

A

occur when a gene has more than two alleles

20
Q

pleiotrophy

A

the property of a gene that causes it to have multiple phenotypic effects

21
Q

epistasis

A

a gene at one locus alters the effects of a gene at another locus

22
Q

polygenic inheritance

A

two or more genes have an additive effect on a single character in the phenotype

23
Q

pedigree

A

a diagram that shows the relationship between parents and offspring across two or more generations. Circles represent females and squares represent males.

24
Q

recessively inherited disorders

A

require two copies of the defective gene for the disorder to be expressed

25
Q

cystic fibrosis

A

caused by a mutation in an allele that codes for a cell membrane protein that functions in the transport of chloride ions into and out of the cells. the resulting high extracellular levels of chloride cause mucus to be thicker and stickier, leading to organ malfunction and recurrent bacterial infections

26
Q

tay-sachs disease

A

is caused by an allele that codes for a dysfuntional enzyme, which is unable to break down certain lipids in the brain. as they accumulate in the brain cells, the child suffers from blindness, seizures, and degeneration of brain function, leading to death

27
Q

sickle cell disease

A

caused by an allele that codes for a mutant hemoglobin molecule that forms long rods when the oxygen levels in the blood are low these long rods cause the red blood cell to sickle, clogging small blood vessels and leading to pain, organ damage, and even paralysis

28
Q

lethal dominant alleles

A

require only one copy of the allele in order for the disorder to be expressed. usually, only late-acting lethal alleles are passed on

29
Q

huntingtons disease

A

caused by a lethal dominant allele. it is a degenerative disease of the nervous system, which usually doesn’t affect the individual until he or she is over 40years old

30
Q

amniocentesis

A

occurs when the physician removes amniotic fluid from around the fetus. the amniotic fluid can be utilized to detect some genetic disorders, and the cells in the fluid can be cultured for a karyotype

31
Q

chorionic villus sampling

A

involves using a narrow tube inserted through the cervix to suction out a tiny sample of the placenta that contains only fetal cells. a karyotyp can immediately be developed from these cells