Chapter 20: Patterns of Variation and Inheritance Flashcards

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1
Q

What is chlorosis and what are the causes?

A
  • Leaves look pale yellow due to cells not producing enough chlorophyll.

Causes:

  • Lack of light.
  • Mineral deficiencies.
  • Viral infections.
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2
Q

Define genotype.

A
  • Alleles that code for a characteristic.
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3
Q

Define phenotype.

A
  • The physical characteristics.
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4
Q

State difference between homozygous + heterozygous genotype.

A
  • Homozygous = two identical alleles for a characteristic.

- Heterozygous = two different alleles for a characteristic where the dominant allele will be expressed.

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5
Q

Define monogenic inheritance.

A
  • Characteristic inherited on a single gene.
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6
Q

Describe codominance.

A
  • Two different alleles occur for a gene –> both equally dominant.
  • Both expressed on phenotype of organism if present.
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7
Q

Name an example of a sex linked disease and state the genotypes for males + females.

A
  • Haemophilia.
  • X^h Y= infected male
  • X^H Y = normal male
  • X^H X^H = normal female
  • X^H X^h = carrier female.
  • X^h X^h = infected female.
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8
Q

Define dihybrid inheritance.

A
  • Inheritance of two characteristics controlled by different genes.
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9
Q

Name an example of dihybrid inheritance + state genotypes.

A
  • Peas.
  • Y = allele coding for yellow seeds.
  • y = allele coding for green seeds.
  • R = allele coding for round seeds.
  • r = allele coding for wrinkled seeds.
  • F2 generation –> ratio of 9:3:3:1 for yellow rounded:yellow wrinkled:green rounded: green wrinkled.
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10
Q

Why is actual ratio of offspring in F2 gen for peas different to expected 9:3:3:1 ratio.

A
  • Random fertilisation of gametes.
  • Genes being studied are on same chromosomes –> linked genes –> inherited together if no crossing over occurs.
  • New allele combinations created.
  • Sample size too low.
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11
Q

Define linkage.

A
  • Genes that code for different characteristics are present at different gene loci on same chromosome.
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12
Q

Define recombinant offspring.

A
  • Different combination of alleles than each parent.
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13
Q

What does the chi-squared test measure?

A
  • The difference between the expected results and the observed results.
  • Tests the null hypothesis.
  • Small chi-squared < critical value at 5% –> little difference between observed + expected –> differences due to chance.
  • Large chi-squared > critical value at 5% –> reject H0 –> significant difference between observed + expected.
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14
Q

Define epistasis.

A
  • Interaction of genes at different loci.

- Multi-step interaction.

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15
Q

What is a hypostatic gene?

A
  • Gene that is affected by another gene.
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16
Q

What is an epistatic gene?

A
  • Gene that affects the expression of another gene.
  • Masks expression –> lack of substrate available to bind to active site of next enzyme in pathway –> less enzyme produced.
17
Q

What are the conditions required for the Hardy-Weinberg Principle to be valid.

A
  • No mutations –> constant allele frequency.
  • Isolated pop.
  • Random mating within pop.
  • Large pop.
  • Characteristic being studied is not sex linked.
  • No selection pressures of any type.
18
Q

What are the factors affecting evolution.

A
  • Mutation
  • Sexual selection = increase in allele frequency of alleles that increase reproductive success.
  • Gene flow.
  • Genetic drift in small pops.
  • Natural selection.
19
Q

Outline stabilising selection.

A
  • Increase in frequency of normal (positive) alleles –> selected for.
  • Decrease in frequency of extreme (negative) alleles –> selected against.
20
Q

Outline directional (natural) selection.

A
  • Change in environment –> normal allele no longer most advantageous.
  • Extreme allele becomes more advantageous + is selected for.
  • Leads to evolution.
21
Q

Outline disruptive selection.

A
  • Extremes selected for and norms selected against.
22
Q

Outline the process of allopatric speciation.

A
  1. Geographical isolation to separate gene pools –> no interbreeding between pops.
  2. Variation due to mutation.
  3. Natural selection –> different selection pressures –> those with most advantageous alleles survive + reproduce passing advantageous alleles to offspring.
  4. Increase in allele frequency of advantageous allele + decrease in disadvantageous allele.
  5. Repeats over many generations.
23
Q

Outline sympatric speciation.

A
  • Geographical isolation not needed for reproductive isolation.
  • Random mating leads to reproductive isolation.

Post-zygotic barrier:

  • After fertilisation –> reduces reproductive viability of offspring –> hybridisation –> infertile offspring.

Prezygotic barrier:

  • Prevent fertilisation + formation of zygote.
  • E.g. geographical isolation, anatomical, seasonal and behavioural changes.
  • Rare because organisms are exposed to same selection pressures.
24
Q

Outline steps of artificial selection/selective breeding.

A
  1. Select organisms with desired traits.
  2. Breed them.
  3. Monitor offspring + select those who exhibit the desired characteristic.
  4. Interbreed to offspring.
  5. Repeat for many generations.
25
Q

Issues with selective breeding.

A
  • Reduces gene pool.
  • Inbreeding.
  • Reduced genetic diversity.
  • Loss of potentially useful alleles.
  • Increased susceptibility to disease.
26
Q

Issues with inbreeding.

A
  • Many genetic disorders are caused by recessive alleles.
  • Decreased genetic diversity + gene pool.
  • Large GD –> recessive alleles masked –> heterozygous individuals.
  • More closely related individuals same homozygous alleles.
  • More likely to get genetic disorders + increased susceptibility to disease.