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Identifying Simple Dominant and Recessive Traits in Pedigrees

This document provides information about identifying dominant and recessive traits in pedigrees. It defines the components of a pedigree such as squares for males and circles for females. It also provides hints for analyzing pedigrees such as if an individual shows a dominant trait, at least one parent must have the dominant phenotype. Examples are also given analyzing autosomal recessive and dominant traits through pedigrees.

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Gwyne Shenette Karylle Noscal
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311 views

Identifying Simple Dominant and Recessive Traits in Pedigrees

This document provides information about identifying dominant and recessive traits in pedigrees. It defines the components of a pedigree such as squares for males and circles for females. It also provides hints for analyzing pedigrees such as if an individual shows a dominant trait, at least one parent must have the dominant phenotype. Examples are also given analyzing autosomal recessive and dominant traits through pedigrees.

Uploaded by

Gwyne Shenette Karylle Noscal
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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Name ____________________________________

Date________________ Period_______

Identifying Simple Dominant and Recessive Traits in Pedigrees


Introduction: A pedigree is a visual chart that depicts a family history or the transmission of a specific trait.
They can be interesting to view and can be important tools in determining patterns of inheritance of specific
traits. Pedigrees are used primarily by genetic counselors when helping couples decide to have children when
there is evidence of a genetically inherited disorder in one or both families. They are also used when trying to
determine the predisposition of someone to carry a hereditary disease for example, familial breast cancer.

The Components of a Pedigree:

Squares are used to indicate males in a family.

Circles are used to indicate females.

If the individual is “affected" by the trait (dominant or recessive) we darken the shape.

A line between a male and a female indicates a marriage or union.

A line drawn down from the marriage line indicates offspring.

Sometimes, you will see some shapes filled in only half way -
this notation indicates a hybrid (heterozygous) or carrier of the trait.

Analyzing Simple Pedigrees:

A pedigree is just like a family tree except that it focuses on a specific genetic trait. A pedigree usually only
shows the phenotype of each family member. With a little thought, and the hints below, you may be able to
determine the genotype of each family member as well!

1
Hints for analyzing pedigrees:

1) If the individual is homozygous recessive, then both parents MUST have at least
one recessive allele (parents are heterozygous or homozygous recessive).

2) If an individual shows the dominant trait, then at least one of the parents MUST have the
dominant phenotype. This one will be pretty obvious when you look at the pedigree.

3) If both parents are homozygous recessive, then ALL offspring will be homozygous recessive.

NOTE: In a pedigree, the trait of interest can be dominant or recessive. The majority of harmful genetic
conditions are only seen when an individual is homozygous recessive - examples of conditions caused by recessive
alleles include cystic fibrosis (a disease of the secretory glands, including those that make mucus and sweat),
Falconi anemia (a blood disorder), albinism (a lack of pigmentation), and phenylketonuria (a metabolic disorder).
Some genetic conditions are caused by dominant alleles (and may therefore be expressed in homozygous dominant
or heterozygous individuals)- examples of conditions caused by dominant alleles include polydactyly (presence of
extra fingers), achondroplasia (a type of dwarfism), neurofibromatosis (a nervous disorder), and a disease known
as familial hypercholesterolemia in which affected individuals suffer from heart disease due to abnormally high
cholesterol levels

Human Pedigrees
For Questions 1-9, use the pedigree chart shown below. Some of the labels may be used more than once.

________ 1. A male
2. A female
________ 3. A marriage

4. A person who expresses the trait


5. A person who does not express the trait
6. A connection between parents and offspring

________ 7. How many generations are shown on this chart?


Assuming the chart above is tracing the dominant trait of "White Forelock (F)" through the family. F is a tuft of
white hair on the forehead.
________8. What is the most likely genotype of individual “A”? (FF, Ff or ff?)
________9. What is the most likely genotype of individual “C”? (FF, Ff or ff?)

Example 1: Tracing the path of an autosomal recessive trait

Trait: Falconi anemia


Forms of the trait:
 The dominant form is normal bone marrow function - in other words, no anemia.
 The recessive form is Falconi anemia. Individuals affected show slow growth, heart defects,
possible bone marrow failure and a high rate of leukemia.
2
A typical pedigree for a family that carries Falconi anemia. Note that carriers are not indicated with half-
colored shapes in this chart.

Ff

ff

Ff

F-
Analysis Questions.

To answer questions #1-5, use the letter "f" to indicate the recessive Falconi anemia allele, and the letter "F" for
the normal allele.

1. What is Arlene's genotype?

2. What is George's genotype?

3. What are Ann & Michael's genotypes?

4. Most likely, Sandra's genotype is .

5. List three people from the chart (other than George) who are most likely carriers of Falconi anemia.

*Example 2: Tracing the path of an autosomal dominant trait

Trait: Neurofibromatosis
Forms of the trait:
 The dominant form is neurofibromatosis, caused by the production of an abnormal form of the protein
neurofibromin. Affected individuals show spots of abnormal skin pigmentation and non-cancerous
tumors that can interfere with the nervous system and cause blindness. Some tumors can convert to a
cancerous form.
 The recessive form is a normal protein - in other words, no neurofibromatosis.
3
A typical pedigree for a family that carries neurofibromatosis is shown below. Note that carriers are not
indicated with half-colored shapes in this chart. Use the letter "N" to indicate the dominant neurofibromatosis
allele, and the letter "n" for the normal allele.

nn

nn Nn

nn N-

Analysis Questions:

1. Is individual #1 most likely homozygous dominant or heterozygous? Explain how you can tell.

2. What is the genotype of individual #3?

3. Can you be sure of the genotypes of the affected siblings of individual #3? Explain.

__________________

Links for (Optional) Extra Practice:


http://learn.genetics.utah.edu/content/addiction/genetics/pi.html
http://www2.edc.org/weblabs/WebLabDirectory1.html (clink on “Genetic Counselor” for pedigrees)
http://www.zerobio.com/drag_gr11/pedigree/pedigree4.htm
http://www.zerobio.com/drag_gr11/pedigree/pedigree_quiz.htm

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