6.2 - Patterns of inheritance Flashcards

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1
Q

Continuous vs discontinuous variation

A

Continuous

  • no defined categories/distinct groups
  • there is a range - any value is possible
  • caused by more than one gene (polygenic) and often, the environment
  • the greater the number of gene loci contributing to the characteristic, the greater the range in variation
  • quantitative

Discontinuous

  • discrete categories with no intermediates
  • usually caused by one gene (mongenic)
  • genes at different loci may interact to influence one characteristic and cause discontinuous variation (epistasis)
  • no (very little) environmental effects cause it
  • qualitative
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2
Q

Environmental factors that influence variation

A
  • Diet in animals can lead to changes in mass/malnutrition
  • Language
  • Scars
  • Plants grown in too little light experience etiolation - rapidly growing  stems, weakening of cell walls, chlorosis (lack of chlorophyll  production). In chlorosis the environmental factors prevent the expression of genes for chlorophyll production
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3
Q

How is genetic variation produced

A
  • Mutations e.g. substitutions change the DNA base sequence
  • Which leads to changes in primary structure of protein and therefore their shape and function
  • Independent assortment of homologous chromosomes in metaphase
  • Independent assortment of chromatids in metaphase II
  • This produces large number of allele combinations
  • Crossing over in prophase
  • so chromatids will have new combination of alleles
  • Non-disjunction means homologous chromosomes don’t separate in metaphase
  • which can cause one more/less chromosome to be present in gamete and subsequent zygote (causes Down’s syndrome)
  • Random fusion of non-genetically identical gametes at fertilisation produces a large number of allele combinations
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4
Q

2 types of natural selection:

A

Stabilising selection

  • occurs when organisms’ environment doesn’t change
  • favours intermediate phenotypes (over extremes)
  • reduces variation in a population
  • e.g. animals with very short/long fur in constant temperatures will be selected against - those with mid length fur will survive - higher frequency of alleles for mid length fur

Directional selection

  • occurs when environment changes
  • favours a new (extreme) phenotype
  • causes a change in population mean phenotype
  • e.g. climate temperature decreases. Those with long fur survive, breed and pass on allele for long hair - over time this allele becomes more frequent in population
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5
Q

2 special types of genetic drift

A

Genetic bottleneck

  • an event e.g. flood rapidly reduces the numbers of a population
  • some alleles lost from population at random
  • genetic variation reduced - genetic drift

Founder effect

  • a small number of individuals from an original larger population establish a new population
  • some alleles lost from population at random (these could be advantageous)
  • genetic variation reduced - genetic drift
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6
Q

Why does genetic drift only happen in small populations?

A
  • Each individual forms a large proportion of the gene pool
  • therefore has a greater effect on the gene pool.
  • It is also easier to ‘lose’ a gene from a small gene pool
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7
Q

2 types of isolating mechanisms that cause speciation

A

Geographical isolation leads to allopatric speciation

  • Populations are physically separated e.g. by water/mountains/fences
  • Barrier prevents gene flow between populations
  • Genetic changes occur in species
  • caused by genetic drift, mutations or natural selection (different pressures in different areas)
  • Ultimately the populations become genetically so different they can no longer interbreed to produce fertile offspring (reproductively isolated) - new species have been formed

Reproductive isolation leads to sympatric speciation

  • Several things can lead to individuals in a population becoming reproductively isolated :
  • Behavioural changes e.g. changes to sleep patterns, courtship behaviours
  • Biological changes e.g. size differences, genetalia differences
  • Genetic changes e.g. change in chromosome number prevents zygote viability
  • Once populations can no longer interbreed to produce fertile offspring (reproductive isolation) - new species have been formed
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8
Q

Stages of selective breeding (artificial selection):

A
  1. male and female with desired characteristic chosen
  2. male and female interbred
  3. best offspring selected and interbred
  4. this is repeated over many generations
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9
Q

Principles behind selective breeding (artificial selection)

A

Humans chose parents with desired phenotypes and therefore the desired alleles and interbreed them to produce offspring with higher frequency of these phenotypes. Repeated over many generations

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10
Q

The importance of maintaining a resource of genetic material for use in selective breeding including wild types (the original population you bred from):

A
  • Selective breeding tends to reduce the gene pool
  • This could mean if there was a rapid environmental change e.g. temperature/disease - genetically similar e.g. crops would not have the variation needed to survive
  • We use gene banks (seed/sperm/egg banks/embryo, rare breed farms, botanic gardens/zoos) to maintain a source of alleles for future breeding
  • This can counteract the loss in genetic variation, inbreeding, and extinction in the event of a disease etc
  • It can also preserve currently unknown useful traits/alleles e.g. medicinal uses
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11
Q

Problems with and how to avoid inbreeding in selective breeding/artificial selection

A
  • As the genetic diversity decreases with each generation, individuals become more and more related - inbred
  • The likelihood of unintentionally selecting 2 copies of a harmful recessive allele can increase in a small gene pool.
  • This can lead to increased susceptibility to disease
  • To avoid this, breeders can ‘outcross’ individuals with their wild types (or individuals from gene banks) to prevent the gene pool becoming too small
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12
Q

Ethical considerations of selective breeding/artificial selection

A
  • Often doesn’t take into account animal welfare
  • Inbreeding can increase susceptibility to disease e.g. some breeds are highly susceptible to cancers
  • Many domesticated animals e.g. pigs would not survive if released into the wild - easy prey, wrong fat:muscle ratio to survive in cold
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13
Q

Explain how selectively breeding for one trait may result in many differences between selectively bred and wild animals

A
  • selective breeding involves whole genomes
  • hence other traits follow selected trait(s)
  • for example, selecting for one trait may inadvertently select for another linked gene
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14
Q

(Generally) how to do any Hardy Weinberg Q

A
  1. Work out the proportion of individuals with the recessive phenotype (=q2)
  2. Work out q (square root of q2)
  3. Work out p (1-q=p)
  4. Use p and q to work out the proportions asked for by the question (e.g. to work out the frequency of heterozygotes: 2pq = 2 x p x q
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15
Q

Monohybrid inheritance

A
  • Inheritance of 1 gene (one trait e.g. eye colour)
  • 2 alleles – 1 dominant and 1 recessive
  • 3:1 (AA,AB,BB)
  • Look out for: 1 trait, only 2 phenotypes
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16
Q

Multiple alleles

A
  • Inheritance of 1 gene (one trait)
  • 3 or more alleles – there may be a dominance hierarchy
  • Look out for: 1 trait, multiple phenotypes
  • e.g. ABO blood groups (also show codominance)
17
Q

Sex linkage

A
  • Inheritance of 1 gene (one trait)
  • Look out for: a clear difference between male and female proportions
  • Written e.g. XAXa for females, XAY for males (no allele on Y)
18
Q

Codominance

A
  • Inheritance of 1 gene (one trait)
  • 2 (or more) alleles – neither dominant over the other – both alleles contribute to the phenotype of the heterozygote
  • 1:2:1 (AA, AB, BB)
  • Look out for: 1 trait, 3 (or more) phenotypes (heterozygous phenotype often appears to be 2 other phenotypes ‘combined’)
  • Written e.g CACA (A’s phenotype), CACB (AB’s phenotype), CBCB B’s phenotype)
19
Q

Dihybrid

A
  • Inheritance of 2 genes (two traits)
  • Genes are NOT linked
  • Genes do NOT have an effect on each other
  • 2 (or more) alleles for each gene – 1 dominant and 1 recessive for each gene
  • 9:3:3:1
  • Look out for: 2 traits expressed in each of 4 phenotypes (e.g. long and yellow)
  • Written: AABB, AaBb (i.e. 2 alleles for each gene)
20
Q

Autosomal linkage

A
  • Inheritance of 2 genes (two traits) on the same chromosome – inherited together
  • Genes do NOT have an effect on each other
  • 2 (or more) alleles for each gene – 1 dominant and 1 recessive for each gene

Autosomal linkage when crossing over has not occurred – what we expect:

  • Look out for: 2 traits expressed in each of 2 phenotypes (e.g. long and yellow)
  • 3:1 (same as a monogenic cross because genes are linked and inherited together)

Autosomal linkage when crossing over has occurred:

  • Crossing over produces recombinant gametes/phenotypes
  • Look out for: 2 traits expressed in each of 4 phenotypes (e.g. long and yellow)
  • A NON 9:3:3:1
  • The further apart the gene loci for the linked genes, the more likely crossing over is and the higher the number of recombinant phenotypes
21
Q

Epistasis

A
  • Inheritance of 2 genes but 1 trait
  • Genes are NOT linked
  • Allele from one gene masks the expression of alleles on another gene
  • 2 (or more) alleles for each gene – 1 dominant and 1 recessive for each gene
  • Modified 9:3:3:1
  • 9:3:4 recessive epistasis (homozygous recessive on one gene is epistatic to alleles on other gene)
  • 12:3:1, 13:3 dominant epistasis
  • 9:7 or 9:3:4 epistasis by complementary gene action
  • Look out for: 1 trait expressed in each of 2/3 phenotypes
  • Written: AABB, AaBb (i.e. 2 alleles for each gene)