CH 2 Basic Inheritance Pedigree Analysis

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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

• He published the results and his interpretation in its


scientific journal in 1866

• Mendel’s paper contains the first clear exposition of the


statistical rules governing the transmission of hereditary
elements from generation to generation

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Each parent has two copies of the
genetic information=homozygous

Each gamete contains only one


copy of the genetic information

Random fertilization unites one copy


from each parent

So the F1 progeny contains two


different variants (alleles) of the
gene = heterozygous

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Dominance:
All F1 offspring produce round seeds
although their genotype is “Ww” because
“W” is dominant and “w” is recessive

The genotypic ratio of the F2 is


1/4 WW
2/4Ww
1/4ww

The phenotypic ratio of the F2 is


3/4 Smooth
1/4 Wrinkled
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Round vs. Wrinkled: Modern Context

• The gene that determines the shape of a seed encodes


an enzyme, starch-branching enzyme I (SBEI), required
to synthesize a branched-chain form of starch known as
amylopectin

• Round (W) seeds contain amylopectin and shrink


uniformly as they dry

• Wrinkled (w) seeds have a mutation in the starch-


branching enzyme I (SBEI) and cannot make
amylopectin and shrink irregularly

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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?

We cross this organism with one we know is homozygous


recessive. Then, the phenotypes of the can be attributed
solely to the gene they inherited from the Unknown parent.
• If the unknown is WW, all
the progeny of the testcross
will be Ww (dominant)
?
unknown
progeny

• If the unknown is Ww, 1/2


the progeny of the testcross
will be Ww (dominant) and
1/2 the progeny will be ww
(recessive)… As in the case
shown on the right.
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Dihybrid Cross
• two different traits, such as seed color (yellow vs. green) and seed
shape (round vs. wrinkled) in the same cross = dihybrid cross
• Breed F1 that you know are hybrid for both characteristics

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

What fraction would we expect to be


Round AND Green
3/4 x 1/4 =
3/16

Addition Rule: The probability that one or


the other of two mutually exclusive events,
A or B, is the sum of their separate
probabilities

What fraction would we expect to be


(Round and Green) OR (wrinkled and yellow)
3/16 + 3/16 =
6/16
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Pertubations on the
theme
• Incomplete dominance = the phenotype of the
heterozygous genotype is intermediate between
the phenotypes of the homozygous genotypes

• Codominance means that the heterozygous


genotype exhibits the traits associated with both
homozygous genotypes
(ABO blood groups are specified
by three alleles IA, IB and IO)
• Penetrance refers to the proportion of organisms
whose phenotype matches their genotype for a
given trait. A genotype that is always expressed
has a penetrance of 100 percent MutS and colon cancer

• Epistasis refers to a gene interaction that results


in a modified F2 dihybrid ratio other than 9 : 3 : 3
: 1. One gene essentially masks the expression
of the other.

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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?

Both individuals are carriers (heterozygous)


for the recessive allele, so there is 1/4 chance
the next child will be affected.

If individual III1 and III7


were to have a child,
what’s the probability that
the child will be affected?

IF both individuals are heterozygous for the


recessive allele, there is 1/4 chance the next
child will be affected.

There is a 1/2 chance III1 is a carrier AND a


1/2 chance that III7 is a carrier AND a 1/4
chance that their child would be affected if
they are carriers.

1/2 X 1/2 X 1/4 = 1/16

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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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