Ch.15: Chromosomes and Inheritance Flashcards

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1
Q

Mitosis and meiosis were first described in

A

late 1800s

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2
Q

The chromosome theory of inheritance states:

A

Mendelian genes have specific loci (positions) on chromosomes
Chromosomes undergo segregation and independent assortment

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3
Q

The behavior of chromosomes during meiosis was said to account for Mendel’s

A

law of segregation and law of independent assortment

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4
Q

an embryologist
Particular genes are on particular chromosomes
Still didn’t know about DNA

A

Thomas hunt morgan

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5
Q

What did Morgan worked with?? It is a model organisms that has certain characteristics that are easily observed such as eye color

A

fruit flies

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6
Q

Several characteristics make fruit flies a convenient organism for genetic studies:

A

They breed at a high rate
A generation can be bred every two weeks
They have only four pairs of chromosomes

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7
Q

or normal, phenotypes

Types that were common in the fly populations

A

wild type

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8
Q

Traits alternative to the wild type are called

A

mutant phenotypes

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9
Q

In one experiment, Morgan mated male flies with white eyes (mutant) with female flies with red eyes (wild type)
The F1 generation all had red eyes
The F2 generation showed the 3:1 red:white eye ratio, but only males had white eyes
Morgan determined that the white-eyed mutant allele must be located on the ____________

A

x chromosome

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10
Q

A gene located on either sex chromosome is called a

A

sex-linked gene

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11
Q

Some disorders caused by recessive alleles on the X chromosome in humans:

A

Color blindness
Duchenne muscular dystrophy
Hemophilia

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12
Q

For a recessive sex-linked trait to be expressed

A

A female needs two copies of the allele

A male needs only one copy of the allele

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13
Q

sex-linked recessive disorders are much more common in

A

males than females

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14
Q

The production of offspring with combinations of traits differing from either parent

A

gene recombination

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15
Q

Offspring with a phenotype matching one of the parental phenotypes are called

A

parental types

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16
Q

Offspring with nonparental phenotypes (new combinations of traits) are called

A

recombinant types or recombinants

17
Q

3 types Types of Chromosomal Alterations

A

Nondisjunction
Aneuploidy
Alteration of Chromosome Structure

18
Q

pairs of homologous chromosomes do not separate normally during meiosis
As a result, one gamete receives two of the same type of chromosome, and another gamete receives no copy

A

nondisjunction

19
Q

results from the fertilization of gametes in which nondisjunction occurred
Offspring with this condition have an abnormal number of a particular chromosome

A

aneuploidy

20
Q

zygote has only one copy of a particular chromosome

A

monosomic

21
Q

zygote has three copies of a particular chromosome

A

trisomic

22
Q

is an aneuploid condition that results from three copies of chromosome 21

A

downs syndrome

23
Q

the result of an extra chromosome in a male, producing XXY individuals

A

klinefelter syndrome

24
Q

Monosomy X, called ______ _______, produces X0 females, who are sterile; it is the only known viable monosomy in humans
Only possible because it occurs on sex chromosomes

A

Turners syndrome

25
Q

is a condition in which an organism has more than two complete sets of chromosomes
Triploidy (3n) is three sets of chromosomes
Tetraploidy (4n) is four sets of chromosomes
common in plants not animals

A

polyploidy

26
Q

Breakage of a chromosome can lead to four types of changes in chromosome structure:

A

Deletion removes a chromosomal segment
Duplication repeats a segment
Inversion reverses a segment within a chromosome
Translocation moves a segment from one chromosome to another

27
Q

The syndrome cri du chat (“cry of the cat”), results from a specific deletion in

A

chromosome 5

28
Q

are genes found in organelles

Mitochondria and chloroplasts carry small circular DNA molecules

A

extranuclear genes or cytoplasmic genes

29
Q

Extranuclear genes are inherited

A

maternally because the zygote’s cytoplasm comes from the egg.

30
Q

What are some examples of Some defects in mitochondrial genes prevent cells from making enough ATP and result in diseases that affect the muscular and nervous systems

A

mitochondrial myopathy and Leber’s hereditary optic neuropathy