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Pedigree Analysis

Classical Genetics

• Mendelian inheritance describes


inheritance patterns that obey two laws
– Law of segregation
– Law of independent assortment
• Simple Mendelian inheritance involves
– A single gene with two different alleles
– Alleles display a simple dominant/recessive
relationship
• Consider, for example, the traits that Mendel studied
Wild-type (dominant) allele Mutant (recessive) allele
Purple flowers White flowers
Axial flowers Terminal flowers
Yellow seeds Green seeds
Round seeds Wrinkled seeds
Smooth pods Constricted pods
Green pods Yellow pods
Tall plants plants

• Another example is from Drosophila


Wild-type (dominant) allele Mutant (recessive) allele
Red eyes White eyes
Normal wings Miniature wings
• Human genetic diseases caused by
recessive mutant alleles
– The mutant alleles do not produce fully
functional proteins
Lethal Alleles
• Essential genes are those that are
absolutely required for survival
– The absence of their protein product leads to a
lethal phenotype
• It is estimated that about 1/3 of all genes are
essential for survival
• Nonessential genes are those not
absolutely required for survival
• A lethal allele is one that has the potential
to cause the death of an organism
– These alleles are typically the result of
mutations in essential genes
– usually recessive, but can be dominant
Lethal Alleles
• Many lethal alleles prevent cell division

• Some lethal allele exert their effect later in life


– Huntington disease
• Characterized by progressive degeneration of the nervous
system, dementia and early death
• The age of onset of the disease is usually between 30 to 50

• Conditional lethal alleles may kill an organism only


when certain environmental conditions prevail
– Temperature-sensitive (ts) lethals
• A developing Drosophila larva may be killed at 30 C
• But it will survive if grown at 22 C
• Every gene carries information telling the
body how to make a particular protein.
– Adult cells have two copies of each gene.
– If one copy of the gene doesn’t work, the cell
has a backup.

• New versions of genes can be produced by


mutations
– These new alleles can produce proteins that
either
• Do not work
• Or do something they’re not supposed to
• Thus any condition associated with this is
referred to as a genetic disease
• Cystic fibrosis (CF)
– A recessive disorder of humans
– About 3% of caucasians are carriers
– The gene encodes a protein called the cystic
fibrosis transmembrane conductance
regulator (CFTR)
• The CFTR protein regulates ion transport across
cell membranes
– The mutant allele creates an altered CFTR
protein that ultimately causes ion imbalance
• This leads to abnormalities in the pancreas, skin,
intestine, sweat glands and lungs
Example: Cystic fibrosis
The cell membranes of the cells lining the lungs and air
passages contain CF membrane proteins
Cl-
Cl-

Cell membrane Cl- CF membrane


proteins
Cl-

The CF protein pumps chloride ions from one side of the


membrane to the other
The CF protein produces a higher concentration of chloride
ions on one side of the membrane than the other
Cl- H2O
Cl-
Cl-
Cl-

H2O Cl- H2O

Cell membrane Cl- H2O


H2O
Cl-
H2O

Water molecules follow the chloride ions across the semi-


permeable cell membranes by… …osmosis.
The body uses the CF chloride pump to move water into
secretions like the mucus found in the trachea and sweat.

If your cells cannot make working chloride pumps, your


mucus becomes too thick and sticky due to lack of water

However, to make a functioning chloride pump, each cell


only needs one good copy of the gene for it.

So, cystic fibrosis is recessive


c C

Defective gene Healthy gene


produces non-working produces working
chloride pump chloride pump Cl -

Cl- Cl- Cl-

Cl- Cl- Cl-


Cl-
Cl- Cl-
Cl- This individual does not
suffer from cystic fibrosis,
but is a carrier
Neither copy of the
gene carried by this
individual can c c
produce a working
chloride pump

Cl-
Cl-
Cl -
Cl-
Cl-

This individual will


Cl -

Cl-
Cl- suffer from cystic
Cl- Cl-
fibrosis

REMEMBER: Genes do NOT exist to cause disease…


… defective genes cause disease
Pedigree Analysis

• In the study of human traits, there are


not controlled parental crosses
• Rely on information from family trees
or pedigrees
• Pedigree analysis is used to determine
the pattern of inheritance of traits in
humans
Pedigree
Symbols

Figure 2.10
Pedigree Analysis
• Pedigree analysis is commonly used to
determine the inheritance pattern of human
genetic diseases
• Genes that play a role in disease may exist as
– A normal allele
– A mutant allele that causes disease symptoms
• Disease that follow a simple Mendelian pattern
of inheritance can be
– Dominant
– Recessive
• A recessive pattern of inheritance makes
two important predictions
– 1. Two normal heterozygous individuals will
have, on average, 25% of their offspring
affected
– 2. Two affected individuals will produce
100% affected offspring
• A dominant pattern of inheritance
predicts that
– An affected individual will have inherited the
gene from at least one affected parent
– Alternatively, the disease may have been
the result of a new mutation that occurred
during gamete formation
Figure 2.10

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