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Transcript
Honors Biology
Unit 12 – Genetics
Intro Pedigree Activity
Name: _____________________
Introduction:
A pedigree is a visual chart that depicts a family history or the transmission of a specific trait.
At least, they can be interesting to view and at most, they 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.
NOTE: In a pedigree, the trait of interest can be dominant or recessive. The majority of harmful
genetic traits are only seen when an individual is homozygous recessive. A small number of diseases are
seen in individuals who are homozygous dominant or heterozygous. Examples of these are
achondroplasia type dwarfism, neurofibromatosis nervous disorder, and a disease known as familial
hypercholesterolemia in which affected individuals suffer from heart disease due to abnormally high
cholesterol levels
A line between a male and a female indicates a marriage or union.
A line drawn down from the marriage line indicates offspring.
Sometimes, filling in half of the square or circle indicates a hybrid 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 if an individual is heterozygous or a carrier for the trait.
1) If the individual is homozygous recessive (shaded in), then both parents MUST have at
least one recessive allele.
2) If the individual is dominant (not shaded), 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 recessive, then ALL offspring will be recessive.
Example 1:
Trait: ability to manipulate tongue
Forms of the trait: ability to roll tongue is dominant, non-tongue rollers are recessive
Form of the trait in the heterozygous individual: tongue roller
Heterozygotes are NOT indicated by half shading –you need to figure them out!
On the pedigree above, indicated genotypes for all individuals. If you do not know the complete
genotype, indicate this with a ?
Example 2:
Trait: Skin, hair and eye pigmentation
Forms of the trait: normal pigmentation is dominant, albinism (lack of pigmentation) is recessive
Form of the trait in the heterozygous individual: normal pigmentation
Two unaffected parents have 3 children. The first child, a girl and the second, a boy, have normal
pigmentation. The third child, a girl, has albinism. The third child marries a normally pigmented male and
they have four children. The first three, two girls and one boy, have normal pigmentation. The fourth, a
girl, lacks pigmentation.
Draw a pedigree showing all the individuals above. List the genotypes of as many individuals in the
pedigree as possible. Shade in half of the symbol if the individual is heterozygous or a carrier.
Is it possible to determine the genotype of ALL the family members?______________