Chapter 12 Flashcards

1
Q

Mendel’s “hereditary factors” were genes which are?

A

segments of DNA located along chromosomes.

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2
Q

Chromosome theory of inheritance

A

-Mendelian genes have specific loci on chromosomes
-chromosomes undergo segregation and independent assortment

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3
Q

What evidence did Thomas Hunt Morgan find?

A

a specific gene is with a specific chromosome

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4
Q

Why is Drosophila Melanagaster a convenient organism for genetic studies? (4)

A

-produce many offspring
-new generation every 2 weeks
-have only 4 pairs of chromosomes
-traits are readily visible

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5
Q

Wild-type

A

common phenotype

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6
Q

Mutant phenotypes

A

uncommon phenotype

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7
Q

What was the first mutant phenotypes Thomas Hunt Morgan discovered?

A

fly with white eyes instead of red

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8
Q

When Morgan mated white eye males and red eyed females, the F2 generation?

A

had only males with white eyes

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9
Q

Morgan concluded that?

A

eye color was related to the sex of the fly

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10
Q

The white eyed mutant allele must be on the _____ chromosome

A

X

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11
Q

Morgan’s findings supported?

A

Chromosome theory of inheritance

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12
Q

Where are there regions that are homologous with corresponding regions on the X Chromosome?

A

Ends of the Y chromosome

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13
Q

Sex-linked gene

A

gene located on either sex chromosome

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14
Q

X-linked genes

A

genes on the X chromosome

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15
Q

Because of the complexity of the process of sex determination, ____.

A

many variations exist

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16
Q

Many _____ help determine sex

A

Y-linked genes

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17
Q

X chromosomes have genes for?

A

characters unrelated to sex

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18
Q

What needs to happen in order for a recessive X-linked trait to be expressed?

A

-female needs 2 copies of the allele (homosygous)
-male needs only one copy of the allele (hemizygous)

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19
Q

X-linked recessive disorders are more common in?

A

males

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20
Q

Disorders caused by recessive alleles on X chromosome:

A

-color blindness
-duchenne muscular dystorphy
-hemophilia

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21
Q

In females, the inactive x condenses into a?

A

barr body

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22
Q

If a female is __ for a particular gene located on the ___ chromosome, she will be?

A

heterozygous, X, a mosaic for that character

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23
Q

Each X chromosome has?

A

hundreds of thousands of genes

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24
Q

Linked genes

A

genes located on the same chromosome that tend to be inherited together.

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25
Q

Morgans experiment showed how linkage affects?

A

inheritance of 2 characters

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26
Q

Morgan crossed flies that differed in?

A

body color and wing size

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27
Q

Morgan find that body color and wing size are usually?

A

inherited together in specific combinations

28
Q

Genetic recombination

A

production of offsrping with combinations of traits differing from either parent.

29
Q

Genetic findings of Mendel and Morgan relate to?

A

Chromosomal basis of recombination

30
Q

Mendel observed that combinations of traits in some offspring?

A

differ from either parent

31
Q

parental types

A

offspring with a phenotype matching one of the parental phenotypes

32
Q

recombinant types

A

offspring with nonparental phenotypes

33
Q

50% frequency of recombination is observed for any?

A

2 genes on different chromosomes

34
Q

Morgan proposed that some process must occasionally break the?

A

physical connection between genes on the same chromosome

35
Q

recombinant chromosomes bring alleles together in?

A

new combinations in gametes

36
Q

The abundance of genetic variation is what ___ works upon?

A

natural selection

37
Q

genetic map

A

ordered list of the genetic loci along a particular chromosome

38
Q

The farther apart 2 genes are?

A

the higher the crossover probability and recombinant frequency

39
Q

linkage map

A

genetic map of a chromosome based on recombinant frequency.

40
Q

genes that are far apart on the same chromosome have a recombination frequency near?

41
Q

Genes that are far apart on the same chromosome are physically connected but?

A

genetically unlinked

42
Q

cytogenetic maps

A

indicate the positions of genes with respect to chromosomal features.

43
Q

large-scale chromosomal alterations often lead to?

A

spontaneous abortions or developmental disorders

44
Q

Nondisjuction

A

pair of homologous chromosomes do not separate normally during meiosis or sister chromatids do not separate during meiosis 2.

45
Q

A result of nondisjunction is that one gamete receives?

A

two of the same type of chromosome and another receives none

46
Q

Aneuploidy

A

results from fertilization of gametes in which nondisjunction occurs

47
Q

monosomic zygote

A

has only one copy of a particular chromosome

48
Q

trisomic zygote

A

has 3 copies of a particular chromosome

49
Q

polyploidy

A

condition in which an organism has more than 2 complete sets of chromosomes

50
Q

Polyploid is common in?

51
Q

deletation

A

removes a chromosomal segment

52
Q

duplication

A

repeats a segment

53
Q

inversion

A

reverses orientation of a segment within a chromosome

54
Q

Translocation

A

moves a segment from one chromosome to another

55
Q

A diploid embryo that is ___ for a large deletation is likely missing __ which is generally ___.

A

homozygous, a number of essential genes, lethal

56
Q

Alterations of chromosome __ and ___ are associated with some serious disorders.

A

number, structure

57
Q

Surviving individuals of alternation of chromosomes have?

A

a syndrome, characteristic of the type of aneuploidy

58
Q

down syndrome

A

aneuploid conditions that results from 3 copies of chromosome 21

59
Q

The frequency of down syndrome increases with?

A

age of the mother

60
Q

Klinefelter syndrome is the result of?

A

an extra chromosome in the male, producing XXY

61
Q

About ___ is born with an extra Y chromosome and ___.

A

1/1000 males, does not exhibit any defined syndrome

62
Q

Females with ___ have ____ except ___.

A

Trisomy X (XXX) no unusual physical features, being taller than average

63
Q

Monosomy X is also called

A

Turner syndrome

64
Q

Monosomy X produces?

A

X0 females who are sterile

65
Q

cri du chat

A

results from specific deletion in chromosomes

66
Q

chronic myelogenous leukemia is caused by?

A

translocation of chromosomes