6.2: Patterns of inheritance Flashcards

1
Q

What are mutagens?

A

Increases the rate of mutations

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2
Q

What are physical agents of mutagens?

3x

A
  • X rays
  • Gamma rays
  • UV light
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3
Q

What are chemical agents of mutagens?

3x

A
  • Mustard gas
  • Nitrous gas
  • Benzopyrene (found in tobacco smoke)
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4
Q

What are biological agents for mutagens?

A
  • Some viruses
  • Transposons
  • Food contaminants
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5
Q

What are persistent mutations?

A

Transmitted through many generations without change

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6
Q

What are random mutations?

A

Not directed by a need on the part of the organism in which they occur

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7
Q

What are five types of chromosome mutations?

A
  • Deletion
  • Inversion
  • Translocation
  • Duplication
  • Non-disjuncture
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8
Q

What is deletion?

A

Part of a chromosome, genes and regulatory seuqences, is lost

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9
Q

What is inversion?

A

Sections of chromosome breakas off, turns 180 degrees and joins again
Some genes may be too far away from their regulatory nucleotides to be experienced

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10
Q

What is translocation?

A

Piece of chromosome breaks off, then becomes attached to another chromosome - interferes with the regulation of the gene

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11
Q

What is duplicaton?

A

Piece of chromosome is duplicated
Overexpression is harmful - too many of certain protiens/gene regulatory nucleic acids may disrupt the metabolism

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12
Q

What is non-disjunction?

A

One pair of chromosome fails to separate leaving one gamete with an extra chromosome

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13
Q

What is aneuploidy?

A

Chromosome number is not an exact multiple of the haploid number for that organism
Chromosomes/chromatids fail to separate during meiosis

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14
Q

What is polyploidy?

A

Diploid gamete fertilised by a haploid gamete, the rsulting zygote will be triploid (three sets of chromosomes)

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15
Q

How does genetic variation arise?

A
  • Allele shuffling - swapping of alleles between non-sister chromatids, during crossing over in prophase 1
  • Independent assortment of chromosomes - M1 AND A1
    Independent assortment of chromatids - M2 AND A2
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16
Q

What does random fertilisation of gamtes that are already genetically unique produce?

A

Extensive genetic diversity among the resulting offspring

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17
Q

What is random fusion?

A

Any gamete can potentially combine with any female gamete from an organism of the same species

18
Q

What are beneficial mutations?

A

Helped drive evolution through natural selection

19
Q

Why were blue eyes a beneficial mutation?

A

Help people see better in less bright light in temperate zones
BUT
Harmful in areas where sunlight intensity is higher as a lack of iris pigmentation could lead to lens cataracts

20
Q

Why was paler skin in temperate zones and darker skin in Africa benefical mutations?

A

High concentration of melanin protected early humans in Africa from sunburn and skin cancer
Temperate conditions: paler skin would be an advantge enabling vitamin D to be made with a lower intensity of sunlight - protects us from heart disease and cancer

21
Q

What are neutral mutations?

A

Neither harmful or benefical

  • Inability to smell certain flowers
  • Differently shaped ear lobes
22
Q

What are four types of variation?

A
  • Interspecific
  • Intraspecific
  • Continuous
  • Discontinuous
23
Q

What is interspecific variance?

A

Between two species

24
Q

What is intraspecific variance?

A

Within species

25
Q

What is variation caused by?

A

Genetic differences or the influence of the environment

26
Q

What is discontinuous variation?

A

Controlled solely by genetics

e.g human blood type

27
Q

What is continuous variation?

A

Caused by multiple genes and the environment working together e.g height/mass of an organism

28
Q

What are features of continuous variation?

A
  • Presented in a histogram
  • No distinct categories
  • Data is quantitive
29
Q

What are features of discontinuous variation?

A
  • Two or more distinct categories
  • No intermediates
30
Q

What is etiolation?

A

Elongation of stem between node, occurs in shaded area to reach light

31
Q

What is chlorosis?

A

Chlorophyll not produced

32
Q

What is monohybrid inheritance?

A

Involves the transmission of one gene from parents to their offspring

33
Q

Where does monohybrid inheritance occur?

A

Gametes (sex cells) because they are haploid, which means that they have one allele per gene

34
Q

What do you have to show before drawing punnet square?

5 things

A

Parental genotypes: Rr x Rr
Parental phenotypes: round round
Gametes produced: Rr Rr
F2 genotypes:

  • R R R r
  • R r r r

F2 phenotypes: round round round round

35
Q

What is F1 generation?

A

The offspring from individuals with homozygous dominant and homozygous recessive genotypes
All the offspring will be heterozygous, inheriting a recessive allele from one parent and a dominant allele from the other
The offspring in the F1 generation will therefore all express the dominant trait in their phenotype

36
Q

What is the F2 generation?

A

Offspring from a two heterozygous F1 individuals
It results in offspring exhibiting a 3:1 ratio of dominant to recessive phenotypes, as shown above.

37
Q

What is the genotypic ratio and phenotypic ratio for monohybrid inheritance?

A

Genotypic: 1:2:1 for RR:Rr:rr
Phenotypic: 3:1

38
Q

What is dihybrid inheritance?

A

Inheritance of two genes therefore 4 alleles

39
Q

What can dihybrid crosses help to do?

A
  • Determine whether genes are linked
  • Locate genes on specific chromosomes
  • Calculate expected phenotypic ratios in subsequent generations
40
Q

What is the ratio in dihybrid inheritance?

41
Q

What are reason why the ratio deviates in dihybrid inheritance?

A

Random fertilisation:
* Gamete fusion is a chance process
* Small sample sizes can lead to skewed ratios, while larger samples minimise these random effects

Linked genes:
* Linked genes are on the same chromosome so alleles are usually inherited together, maintaining the parents’ original allele combinations in offspring.
* However, crossing over during meiosis can sometimes change these allele combinations by separating linked genes.