Ch 15: Chromosomal Basis of Inheritance Flashcards

1
Q

Who developed the Chromosome theory of inheritance?

A

around 1902 Sutton and Boveri and others independently noted the parallels between chroomosme behavior and the behavior of the proposed factors and developed the theory

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2
Q

What is a wild type?

A

normal phenotypes in populations

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3
Q

What is a sex-linked gene?g

A

genes on X and Y chromosomes that code for an individuals sex

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4
Q

What are X-linked genes?

A

genes on the X chromosome, which humans contain about 1,100 genes on their X chromosme

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5
Q

What needs to occur for a recessive X-linked trait to be expressed?

A

a female needs two copies of the allele (homozygous) and a male needs only one copy of the allele (hemizygous)

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6
Q

What are some disorders that are caused by recessive alleles on the X chromosome in humans?

A

color blindness (mostly X-linked), Duchenne muscular dystrophy, and hemophilia

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7
Q

What is the inactivated X (in females) condensed too?

A

a barr body

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8
Q

What are linked genes?

A

genes that are on the same chromosome that tend to be inherited together

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9
Q

What is genetic recombination?

A

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

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10
Q

What are parental types?

A

offspring with a phenotype matching one of the parental phenotypes

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11
Q

What are recombinant types (recombinants)?

A

offspring with nonparental phenotypes (new combinations of traits)

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12
Q

What is crossing over?

A

when genetic material is swapped between chromosomes during prophase

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13
Q

What increases genetic variation?

A

recombinant chromosomes and random fertilization

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14
Q

Who constructed a genetic map?

A

Alfred Sturtevant, one of Morgan’s student’s

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15
Q

What is a genetic map?

A

an ordered list of the genetiv loci along a particular chromosome

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16
Q

What is a linkage map?

A

a genetic map of a chromosome based on recombination frequencies

17
Q

What can distances between genes be expressed as?

A

map units

18
Q

What is nondisjunction?

A

when 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 recieves no copy

19
Q

What is aneuploidy?

A

offspring with an abnormal number of a particular chromosome, resulting nondisjunction

20
Q

What is a monosomic zygote?

A

a zygote with only one copy of a particular chromosome

21
Q

What is a trisomic zygote?

A

a zygote has three copies of a particular chromosome

22
Q

What is polyploidy?

A

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

23
Q

What is triploidy?

A

three sets of chromosomes

24
Q

What is tetraploidy?

A

four stes of chromosomes

25
Q

What are the four types of changes in chromosome structure that results from the breakage of a chromosome?

A

deletion, duplication, inversion, and translocation

26
Q

What is deletion?

A

the removal of a chromosomal fragment

27
Q

What is duplication?

A

repetition of a segment

28
Q

What is inversion?

A

the reverse orientation of a segment within a chromosome

29
Q

What is translocation?

A

the movement of a segment from one chromosome to another

30
Q

What is down syndrome?

A

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

31
Q

What are the two exceptions to standard Mendelian inheritance?

A

genes located in the nucleus and genes located outside the nucleus

32
Q

What is genomic imprinting?

A

the silencing of certain genes depending on which parent passes them on