CH 2 Basic Inheritance Pedigree Analysis
CH 2 Basic Inheritance Pedigree Analysis
CH 2 Basic Inheritance Pedigree Analysis
Transmission Genetics
Heritage from Mendel
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Gregor Mendel
• G. Mendel carried out his experiments from 1856 to 1863
in a small garden plot nestled in a corner of the St.
Thomas monastery in the town of Brno
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3
Each parent has two copies of the
genetic information=homozygous
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Dominance:
All F1 offspring produce round seeds
although their genotype is “Ww” because
“W” is dominant and “w” is recessive
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Monohybrid Genetic Cross
Both F1 parents are
heterozygous for the
gene.
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Testcross A method to figure out the
? genotype of the organism…
Analysis Is this pea WW or Ww?
W w G g
W WW Ww G GG Gg
w Ww ww g Gg gg
WG Wg wG wg
WG WWGG WWGg WwGG WwGg
Wg WWGg WWgg WwGg Wwgg
wG WwGG WwGg wwGG wwGg
wg WwGg Wwgg wwGg wwgg
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Phenotypic ratio of 9/16 : 3/16 : 3/16 : 1/16
Independent Segregation
• The Principle of
Independent
Assortment:
Segregation of the
members of any
pair of alleles is
independent of the
segregation of other
pairs in the
formation of
reproductive cells.
Fig. 2.11
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Probabilities
Multiplication Rule: The probability that two
independent events, A and B, are realized
simultaneously is given by the product of their
separate probabilities
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Epistasis
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Complementation
reveals whether two recessive mutations are alleles of different genes
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Pedigree Analysis
• In humans, pedigree analysis is used to determine
individual genotypes and to predict the mode of
transmission of single gene traits
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Autosomal Dominant Traits
• Huntington disease is a progressive nerve degeneration, usually beginning
about middle age, that results in severe physical and mental disability and
ultimately in death
• Every affected person has an affected parent
• ~1/2 the offspring of an affected individual are affected
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Autosomal Recessive Traits
• Albinism = absence of pigment in the skin, hair, and iris of the eyes
• Most affected persons have parents who are not themselves affected; the parents
are heterozygous for the recessive allele and are called carriers
• Approximately 1/4 of the children of carriers are
affected
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How is this trait
most likely
inherited?
If individual III5 and III6
have another child,
what’s the probability that
the child will be affected?
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How is this trait most If individual III4 and III6 have
a child, what’s the probability Zero
likely inherited? that the child will be affected?
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If the
“nontaster”
allele is
relatively
common in
the
population,
how is this
trait most
likely
inherited?
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How is this trait
most likely
inherited?
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