Chapter 13: Modern Understandings of Inheritance Flashcards

x Explain why two genes close to each other on the same chromosome show a different inheritance pattern than two genes on separate chromosomes. x Use recombination frequencies to determine if two traits are genetically linked, and if so, how closely. x Define various chromosomal abnormalities and describe their potential effects on the organism.

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1
Q

Who is the person whose work influenced modern genetics?

A

Gregor Mendel

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2
Q

Chromosomal Theory of Inheritance

(Background Info)

A

-Proposed before there was any direct evidence that traits were carried on chromosomes
-Scientists, Boveri and Sutton, independently discovered that chromosomes occur in matched maternal and paternal pairs that segregate in meiosis
-They were supported by Eleanor Carothers demonstrating independent assortment of chromosomes in grasshoppers

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3
Q

Chromosomal Theory of Inheritance

A
  • During Meiosis, chromosome pairs migrate as discrete structures
    -Chromosome sorting from each homologous pair into pre-gametes appear to be random
  • Each parent synthesizes gametes that contain only half their chromosomal complement
  • Even though male and female gametes (sperm and egg) differ in size and morphology, they have the same number of chromosomes, suggesting equal genetic contributions from each parent
  • The gametic chromosomes combine during fertilization to produce offspring that have the same number of chromosomes as their parents
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4
Q

Can traits be sex-linked?

A

Yes, T.H. Morgan showed that the white eye mutant allele was inherited along with sex (the x chromsome)

This sex linkage was the first demostration that genes were on chromosomes

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5
Q

The concept of linkage was further extended to map genes to chromesome positons, what is this called?

A

Genetic Linkage Maps

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6
Q

Do traits segregate on the same chromosome?

A

Yes, however, far apart traits segregated independently.

Traits closer together segregated less often than independence predicted

Cross over between homologous chromosomes was the mechanism that segregated genes on the same chromosome. When genes were far apart
crossover happened all the time. When the were close together cross over happened less frequently.

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7
Q

Linked genes

A

They are located close to each other on the same chromosome and tend to be inherited together.

They display different offspring ratios compared to unlinked genes

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8
Q

Independent assortment occurs when?

A

During Meiosis

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9
Q

What type of genes are independently assorted?

A

Unlinked genes

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10
Q

Inheritance patterns of unlinked genes

A
  • 50% parental type offspring and 50% recombinant offsprings
  • 1:1:1:1 ratio of phenotypes
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11
Q

What type of genes are NOT independently assorted?

A

Linked Genes

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12
Q

Inheritance Patterns of linked genes

A
  • No recombinant offsprings, all are parental type
  • 1:1:0:0 ratio of phenotypes
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13
Q

Inheritance Patterns of linked genes

if crossover always occur between homologous chromosomes

A
  • 1:1:1:1 ratio of phenotypes
  • 50% parental type offspring and 50% recombinant offsprings
  • linked genes** ACT LIKE** independently assorted.
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14
Q

Recombination Frequency

A

is the frequency in which a single chromosomal crossover will take place between two genes during meiosis

(recombinants/ total offspring) x 100 = recombination frequency %

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15
Q

What is a Linkage Map?

A
  • Recombination frequencies can be used to map the relative position of geneson chromosomes
  • So, a diagram where relative gene locations are
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16
Q

Genetic Linkage Mapping

A
  • Recombination frequency was a function
    of distance between genes.
  • Recombination of 1% was chosen as a
    unit equal to one genetic map unit (gmu)
    also named a Centimorgan in honor of T.H. Morgan
17
Q

When does abjunction occur?

A

Nonjunction occur when homologous chromosomes or sister chromatids fail to separate during Meiosis, resulting in an abnormal number of chromosomes. Occurs during either Meiosis I or Meiosis II

18
Q

Sex Chromosome Abjunction

(example used is cat fur coat colors)

A

In cats, the fur coat color in on the x chromosome, in the development of
female cats, one of the two X
chromosomes is randomly
inactivated in each cell, resulting in
a tortoiseshell pattern if the cat has
two different alleles for coat color. Because of this male cats cannot have tortoiseshell pattern fur coat

19
Q

Cri-du-chat syndrome- deletion of chromosome

A

A human genetic disorder resulting from a chromosomal recombination mutuation that causes a deletion of a portion of chromosome 5

20
Q

What type of inversion include the centromere?

A

Pericentric Inversion

21
Q

A pericentric inversion can…

A

Change the relative lengths of the chromosome arms

paracentric inversion cannot do this

22
Q

Homologous Pairing: When one chromosome undergoes an inversion, but the other one does not, what must the other chromosome do?

A

The chromosome must form an inverted loop to retain point for point interaction during synapsis

This inversion pairing is essential to maintaining gene alignment during Meiosis and to allow for recombination

23
Q

Reciprocal translocation mutations

A

Non-homologous chromosomes may also exchange material

24
Q

When does a reciprocal translocation occur?

A

Occurs when another segment of DNA is transferred fromm one chromosome to another nonhomologous chromosome