IV. MENDELIAN INHERITANCE (The Pedigree analysis)

A B C
D
Mendel and His
Experiment
Law of Segregation
The Law of
Independent
Assortment
Some Human Traits follow
Mendelian Patterns of
Inheritance in Humans
E F
Some Mendelian
Disorders in Humans
Pedigree Analysis
GENERAL OBJECTIVES: Determine genotypic and phenotypic probabilities
using Punnett square.
IV. MENDELIAN INHERITANCE

IV. MENDELIAN INHERITANCE
A B C
D
Mendel and His
Experiment
Law of Segregation
The Law of
Independent
Assortment
Some Human Traits follow
Mendelian Patterns of
Inheritance in Humans
E F
Some Mendelian
Disorders in Humans
Pedigree
Analysis
GENERAL OBJECTIVES: Determine genotypic and phenotypic probabilities
using Punnett square.

PEDIGREE
ANALYSIS
PREPARED BY: BUSTAMANTE, BEA LYKA TOMASA O.
BS BIOLOGY AB21

Pedigrees is used to analyze the pattern of inheritance
of particular trait throughout a family.
Pedigrees show the presence or absence of a trait as it
relates to the relationship among parents, offspring
and siblings.
What is a
PEDIGREE ANALYSIS ?
Pedigree analysis is therefore an important tool in
basic research and genetic counseling.
Each pedigree chart represents all of the available
information about the inheritance of a single trait
within a family.
PEDIGREE ANALYSIS. Retrieved from. https://www.cs.cmu.edu/genetics/units/instructions-PBA.pdf

Parts of a PEDIGREE CHART
I
II
MARRIAGE LINE
LINE OF
DESCENT
SIBLING LINE
GENERATION NUMBER
FEMALE
MALE
AFFECTED WITH
TRAIT
DECEASED
TWINS
ADOPTED
MISCARRIAGE
Khan academy.(2020).PEDIGREES REVIEW. Retrieved from.
https:www.khanacademy.org/science/high-school-biology/hs-classical-genetics/hs-pedigrees/a/hs-
pedigrees-review.com

This chart shows four generations of a family with four individuals who are
affected by a form of colorblindness.
I
II
III
IV
• Circles represent females and squares represent males.
• Each individual is represented by:
– a Roman Numeral, which stands for the generation in
the family,
– a Digit, which stands for the individual within the
generation.
(For instance, The female at the upper left is individual I-
1.)
• A darkened circle or square represents an individual
affected by the trait.
1
1
1
1
2
2
2
3
3

This chart shows four generations of a family with four individuals who are
affected by a form of colorblindness.
I
II
III
IV
• The “founding parents” in this family are the female I-1 and
the male I-2 in the first generation at the top.
• A male and female directly connected by a horizontal line
have mated and have children.
These three pairs have mated in this tree: I-1 & I-2, II-2 & II-3,
III-2 & III-3
• Vertical lines connect parents to their children. For instance
the females , II-1 and II-2 are daughters of I-1 and II-2
• The “founding family” consists of the two founding
parents and their children, II-1 and II-
1
1
1
1
2
2
2
3
3

 In this pedigree, the unaffected founding mother, I-1, and
affected founding father, I-2, are parents to two affected
daughters, II-1 and II-2.
 The affected founding daughter II-2 and the unaffected male II-
3 who “marries into the family” have two offspring, an
unaffected daughter III-1 and affected son, III-2.
 Finally, this affected male III-2 and the unaffected female III-3
who “marries in” have an unaffected son, IV-1.

Pedigrees are interesting because they
can be used to do some detective work
and are often used to study the genetics
of inherited diseases.
For example, pedigrees can be analyzed to determine
the mode of transmission for a genetic disease:
(1) Dominance - whether the disease alleles
are dominant or recessive;
(2) Linkage - whether the disease alleles are
X-linked (on the X chromosome) or
autosomal

Amoeba Sisters (Feb 9, 2017). PEDIGREES. Retrieved from. https://www.AmoebaSisters.com

General Assumptions
In the problems that follow, you’ll be reasoning about the mode of transmission of genetic traits that
are controlled by one gene, with two alleles, a dominant allele and a recessive allele.
An individual in the pedigree will be affected (express the phenotype associated with
a trait) when the individual carries at least one dominant allele of a dominant trait, or
two recessive alleles of a recessive a trait
In each problem, the trait in question is rare in the general population. Assume for the purposes
of these problems that individuals who marry into the pedigree in the second and third
generations are not carriers. This does not apply to the founding parents – either or both of the
individuals at the top of the pedigree could be carriers.
The causative genes in these problems may be autosomal or X-Linked,
but are not Y-linked.
RARE-IN-
POPULATION
COMPLETE
PENETRANCE
NOT-Y-LINKED
We also make three simplifying assumptions:

4 Key Clues There are five things to remember in reasoning
about pedigrees
(because a single allele of a dominant trait causes an individual to be affected).
(1) An unaffected individual cannot have any alleles of a dominant trait.
they will never be affected and can never be carriers of a recessive trait. (because the trait is rare
in the population)
(2) Individuals marrying into the family are assumed to have no disease alleles
(because two alleles of a recessive trait are required for an individual to be affected)
(3) An unaffected individual can be a carrier (have one allele) of a recessive trait
(because the male is hemizygous – he only has one allele of an X-linked trait)
(4) When a trait is X-linked, a single recessive allele is sufficient for a male to be
affected.

KeyPatternsinPedigree
Analysis

Patterns that
Indicate a
RECESSIVE
Trait
• The disease must be RECESSIVE if any affected
individual has 2 unaffected parents.
• AUTOSOMAL RECESSIVE: If any affected founding daughter
has 2 unaffected parents the disease must be autosomal
recessive.
• RECESSIVE: If an affected founding son has 2 unaffected
parents, we cannot determine if the recessive disease is
autosomal or x-linked.
• X-LINKED RECESSIVE: When an affected
non-founding son has 2 unaffected parents
the disease must be X-linked recessive.

Patterns that
Indicate a
DOMINANT
Trait
• The disease must be DOMINANT if every affected
child of NON-FOUNDING parents has an affected
parent.
• When an affected son of non-founding parents has an affected
father the disease must be AUTOSOMAL DOMINANT.
• When an affected daughter of non-founding parents has an
affected father, we cannot determine whether the DOMINANT
disease is autosomal or x-linked.

ONLINEDIAGNOSIS
Amoeba Sisters (Feb 9, 2017). PEDIGREES. Retrieved from. https://www.AmoebaSisters.com

PEDIGREE ANALYSIS. Retrieved from.
https://www.cs.cmu.edu/genetics/units/instructions-PBA.pdf
REFERENCES
Khan academy.(2020).PEDIGREES REVIEW. Retrieved from.
https:www.khanacademy.org/science/high-school-biology/hs-classical-
genetics/hs-pedigrees/a/hs-pedigrees-review.com
Amoeba Sisters (Feb 9, 2017). PEDIGREES. Retrieved from.
https://www.AmoebaSisters.com

IV. MENDELIAN INHERITANCE (The Pedigree analysis)

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