Quiz 3 (Ch. 8) Flashcards

1
Q

Chromosomes are classified as ______ when the centromere is very close to the center

A

Metacentric

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2
Q

Chromosomes are classified as ______ when the centromere is slightly off center

A

Submetacentric

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3
Q

Chromosomes are classified as ______ when the centromere is significantly off center but not at the end

A

Acrocentric

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4
Q

Chromosomes are classified as ______ when the centromere is at one end

A

Telocentric

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5
Q

What types of features do cytogeneticists use to make a karyotype? (3 things)

A

i) Size of the chromosomes
ii) Placement of the centromere
iii) Banding patterns

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6
Q

Why can mutations in duplications of genes be advantageous?

A

Because the mutations will often lead to a more specified function of the gene. This is advantageous because the specified function will be more efficient at performing that function

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7
Q

What is the removal of a segment of a chromosome called?

A

Deletion

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8
Q

What is the addition of a segment of chromosome called?

A

Duplication

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9
Q

What is it called when a segment of a chromosome is flipped in the opposite orientation?

A

Inversion

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10
Q

What is it called when a chromosomal segment is swapped between nonhomologous chromosomes?

A

Translocation

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11
Q

Euploidy

A

The number of sets of chromosomes in an organism

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12
Q

In what two ways can changes in chromosome number occur?

A

i) Changes in the number of sets of chromosomes (euploidy)

ii) Changes in the number of chromosomes within a set (ex: from 2 in a set to 4 in a set)

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13
Q

What dye is used in G-banding?

A

Giemsa

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14
Q

How is the banding pattern of a chromosome useful? (3 ways)

A

i) It distinguishes individual chromosomes from each other
ii) It detects changes in chromosome structure
iii) It reveals evolutionary relationships among the chromosomes of closely related species

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15
Q

Simple translocation

A
  • A one-way transfer of genetic material

- A piece of a chromosome is attached to another chromosome

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16
Q

Reciprocal translocation

A
  • A two-way transfer of genetic material

- Two different types of chromosomes exchange pieces, producing two abnormal chromosomes with translocations

17
Q

How does a deletion occur?

A

Occurs when a chromosome breaks and a fragment of it is lost

18
Q

How does a deletion affect the phenotype of an organism?

A
  • Generally detrimental
  • The larger the deletion, the more likely the phenotype of the organism will be changed
  • If genes which are vital to the function of the organism are lost, it can be lethal
19
Q

How do duplications occur?

A
  • Caused by abnormal events during recombination

- Repetitive sequences can cause misalignment between homologous chromosomes

20
Q

Nonallelic homologous recombination

A

When a crossover occurs between two misaligned chromosomes

21
Q

Gene family

A
  • Consists of two or more genes that are derived from the same ancestral gene
  • Ex: The globin gene encodes all subunits that bind oxygen
  • –Has 14 paralogs on 3 different chromosomes
22
Q

In what two situations do inversions cause a phenotypic effect?

A

i) Break point effect - If the inversion break point occurs in a vital gene
ii) Position effect - A gene is repositioned in a way in which it affects its expression

23
Q

Explain why an individual who is heterozygous for an inversion may be phenotypically unaffected but is more likely to have a child which is affected by this inversion

A
  • The abnormality in offspring is due to crossing over within the inverted segment
  • During meiosis I, pairs of sister chromatids synapse with each other
  • –For the normal & inversion chromosome to synapse properly, an inversion loop must form
  • –If a crossover occurs within the inversion loop, very abnormal chromosomes are produced (chromosomes having two or no