Ch 11 and 12 Flashcards

1
Q

Mendel’s Model for Inheritance

A

variation in characteristics are from multiple versions of genes, an offspring inherits one allele from each parent per trait, dominant allele determines phenotype

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2
Q

Law of Segregation

A

each gamete gets only one allele

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3
Q

true breeding

A

homozygous dominant or recessive parents

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4
Q

test crossing

A

hybridization by crossing two true breds

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5
Q

monhybrid cross

A

cross of two heterozygous individuals for one trait

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6
Q

dihybrid cross

A

cross of two heterozygous individuals for two traits

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7
Q

law of independent assortment

A

when crossing two traits, they are entirely independent, creating 16 genotypes instead of still just 4

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8
Q

complete dominance

A

one allele determines the phenotype

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9
Q

incomplete dominance

A

combination of alleles creates an inbetween phenotype (red + white = pink)

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10
Q

codominance

A

combination of alleles creates a mix of phenotype (red + white = spotted colors)

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11
Q

epistasis

A

a double trait relationship in which the second trait alters the state of the first

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12
Q

polygenic inheritance

A

a trait combination that is on a spectrum of phenotypes (skin color)

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13
Q

multiple alleles

A

one trait has more than one possible allele (blood type has three)

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14
Q

pleiotropy

A

a single allele combination that determines multiple characteristics

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15
Q

chromosome theory of inheritance

A

the way we knew how inheritance worked: 1. chromosomes and genes are both paired with diploid. 2. alleles separate during meiosis. 3. fertilization restores pairs

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16
Q

Morgan’s experiments: why the fly?

A

used fruit fly, creates hundreds of offspring in one mating, new generation can occur in two weeks, only 4 chromosomes

17
Q

Morgan’s experiments: sex-linked

A

discovered flies with red and white eyes and the ratios of males and females, more males had mutation, X-linked traits

18
Q

Sex-determining region of Y (SRY)

A

a region that must be present to convert ovaries to testes on the Y chromosome

19
Q

X-linked genes

A

have both sex related and non-sex related traits

20
Q

hemizygous

A

because Y has no allele, the X has only one allele for males so it cant be homo or hetero, its hemi

21
Q

X inactivation

A

most of one female X chromosome is inactivated during pregnancy because don’t need double genes

22
Q

linked genes

A

genes located near each other tend to be inherited together

23
Q

Morgan’s experiment: linked genes

A

black body and small wings or gray body and normal wings; when parental frequency is more than 1/2 is it linked

24
Q

recombination of linked genes

A

when offspring have different phenotypes than parents, close genes evidently did cross-over; often creates entirely new genes

25
Q

linkage map

A

shows distance and recombination frequency on genes

26
Q

Chi-square test

A

observed and expected frequency value showing that the frequency differences are due to chance OR due to a genetic pattern; based on df and p=0.05

27
Q

nondisjunction

A

chromosome separation goes wrong; one gamete has two, one has three

28
Q

aneuploidy

A

monosomic = 2n-1; trisomic = 2n+1

29
Q

polyploidy

A

created by trisomic aneuploidy on every chromosome so that the organism is 3n

30
Q

chromosomal deletion

A

fragment of chromosome deleted

31
Q

chromosomal duplication

A

fragment added to a chromosome as an exact copy

32
Q

chromosomal inversion

A

reversed segment within a chromosome

33
Q

translocation

A

moves a chromosome’s section to a nonhomologous chromosome