Title: GENETICS
1GENETICS
1
2Gregor Mendel
- Genetics the branch of biology that deals with
heredity. - A great deal of what we know about genetics began
with the work of a monk named Gregor Mendel, who
experimented with sweet pea plants in the 1800s.
2
3Mendels Work
- Mendel studied the patterns of inheritance in pea
plants. - He chose seven traits to follow.
3
4- Mendel needed to make sure he had plants that
always gave the same offspring-called true
breeding. - He self-pollinated plants until he got seeds
that always gave the same offspring.
4
5- He took a purple flower plant and crossed it with
a white flower plant. - He called these the parent generation (P1
generation) - What do you think the offspring (the F1
generation) looked like?
Pollen
X
ALL PURPLE
5
6POLLEN
F1
SAY WHAT???????
F2
6
7Mendel concluded
- Something is being passed from parent to
offspring. - Sometimes you can see it and sometimes you
cant. - If you can see it- it is dominant.
- If its there and you cant see it- its
recessive.
7
8- Dominant alleles are shown using a capital letter
(R) - Recessive alleles are shown using a lower case
letter (r) - Examples Rred rpink
- RR - ?
- Rr - ?
- Rr- ?
- Each version is called an allele.
8
9Alleles are locted on genes on chromosomes.
9
10Law of Dominance
- States that the dominant allele will prevent the
recessive allele from being expressed. The
recessive allele will only appear when it is
paired with another recessive allele in the
offspring.
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1111
12WHAT WE KNOW NOW
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13We have two copies of all of our chromosomes Why?
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14BOY OR GIRL?
14
15What is a gene?
- A segment on the chromosome that codes for a
protein. - People have two copies of each gene, one copy
inherited from the mother and the other copy
inherited from the father. - There are many versions of each gene-alleles
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16If the two alleles in the pair are identical,
then the condition called homozygous.
If the 2 alleles are different, the condition is
called heterozygous. The term hybrid is
sometimes used to refer to heterozygous.
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17Genotype the genes or alleles (RR, Rr, rr)
Phenotype an organisms physical appearance (Red,
White)
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1818
19How did you end up with the traits and genes that
you got? During meiosis, each egg or sperm only
gets one copy of each chromosome.
19
20A b
a B
Law of Segregation (separation) states that gene
pairs separate when gametes (sex cells) are
formed, so each gamete has only one allele of
each gene pair.
A b
a B
A b
a B
A b
a B
A b
a B
20
21- Law of Independent Assortment
- states that different pairs of genes separate
- independently of each other when gametes are
formed.
Example Just because you get the gene for brown
hair does not mean you will get the gene for blue
eyes.
21
22REVIEW
- A trait is a characteristic an individual
receives from its parents. - Genes carry the instructions responsible for the
expression of traits. - A pair of inherited genes controls a trait.
- One member of the pair comes from each parent.
- Alternative versions of genes are known as
alleles.
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23REVIEWMendels Principles of Inheritance
- Inherited traits are transmitted by genes which
occur in alternate forms called alleles - Principle of Dominance - when 2 forms of the same
gene are present the dominant allele is expressed - Principle of Segregation - in meiosis two alleles
separate so that each gamete receives only one
form of the gene - Principle of Independent Assortment - each trait
is inherited independent of other traits (chance)
23
24Punnett Squares
- Used to determine the probability of a
combination of alleles - Example If a heterozygous black rabbit is
crossed with a heterozygous black rabbit, what
are the chances the offspring will be black?
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25- BBlack
- b Brown
- Genotypes?
- Phenotypes?
25
26Example EOCT Question
- Earlobe shape is a human trait. Some people have
free earlobes while others have attached
earlobes. Two parents with free earlobes have
four children. Three children have free earlobes
and one child has attached earlobes. If these
parents have another child, what is the
probability that the child will have attached
earlobes? - A 25
- B 50
- C 75
- D 100
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27Example EOCT question
- In humans, a widows peak is dominant over a
continuous hairline. Marys father has a widows
peak, but Mary and her mother have a continuous
hairline. What is the genotype of Marys father? - A HH
- B Hh
- C hh
- D cannot be determined
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2828
29Incomplete dominance - cross between organisms
with two different phenotypes that produces
offspring with a third phenotype that is a
blending of the parental traits. Ex. Red and
White Pink
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30 Incomplete Dominance
30
3131
32Codominance
- a cross between organisms with two different
phenotypes produces offspring with a third
phenotype in which both of the parental traits
appear together. - Ex Yellow and Orange yellow with orange spots
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33Codominance
- Both phenotypes are expressed at the same time.
- Example Blood
- Types
Genotype Phenotype
IOIO Type O
IAIO Type A
IAIA Type A
IBIO Type B
IBIB Type B
IAIB Type AB
There are 3 alleles for blood type- multiple
alleles
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34CodominanceR allele for red flowers W
allele for white flowers red x white ---gt red
white spotted
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35Polygenic traits
- Most traits are controlled by many genes, not
just one. - Examples hair color and skin color. There are
several genes that control them. - This is the reason that there are so many
different colors of hair and skin in humans.
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36Sex Linked Traits
- Traits associated with particular sexes are
called sex-linked or X-linked traits. - These are usually carried on the X chromosome.
- Females XX
- Males XY
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371st 22 are Autosomes, the last pair (XY) are sex
chromosomes)
Karyotype
37
38Charts that show relationships within a family
Pedigree
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3939
4040
41Autosomal-Dominant
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42SEX-LINKED
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43SEX-LINKED
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44Autosomal -Dominant
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45Genetic Disorders
45
46Huntingtons Disease
- Huntington's disease degenerative disease that
causes certain nerve cells in your brain to waste
away. - you may experience uncontrolled movements,
emotional disturbances and mental deterioration. - The disorder was documented in 1872 by American
physician George Huntington. - Fatal----ages30-60
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47Colorblindness
- Sex-linked trait
- Gene for color vision located on the X
chromosomes. - Males are more likely to have colorblindness
because they have only one X chromosome
47
48What do you see?
What do you see?
- The individual with normal color vision will see
a 5 revealed in the dot pattern. An individual
with Red/Green (the most common) color blindness
will see a 2 revealed in the dots.
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4949
50TEST
50
51Down Syndrome
- Three copies of chromosome 21.
- Symptoms mental retardation and some physical
deformities
51
52Downs Syndrome How do you get 3 copies of
chromosome 21?
Nondisjunction failure of chromosomes to
separate properly during cell division
52
53Cystic Fibrosis
- caused by a recessive allele on chromosome 7.
- Deletion of three bases.
- Affects the body's respiratory and digestive
systems.
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54 Hemophilia
- Sex-liked, recessive trait
- Located on the X chromosome
- Missing a protein necessary for blood clotting
- Can bleed to death from minor cuts.
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55Queen Victorias Pedigree showing Hemophelia
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56Sickle Cell
People who carry the tendency to have sickle cell
anemia are less likely to die from malaria.
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57Gene Therapy
The insertion of healthy genes into an
individuals cells or tissues to treat a disease.
57
58Example EOCT question
- What is nondisjunction?
- A. failure of chromosomes to separate during
meiosis - B. failure of the cytoplasm to divide properly
- C. the insertion of a gene into a different
chromosome - D. the deletion of a gene from a chromosome
58
59Which of the following shows how information is
transformed to make a protein? A DNA ?RNA ?
protein B gene ? chromosome protein C cell
respiration ? ATP ? protein D ATP ? amino acid ?
protein
59
60Information on mRNA is used to make a sequence of
amino acids into a protein by which of the
following processes? A replication B
translation C transcription D transference
60
61Pea plants have seeds that are either round or
wrinkled. In this cross, what will be
the phenotypic ratio of the offspring?
A 50 RR and 50 Rr B 25 RR, 50 Rr, and 25
rr C 50 round seeds and 50 wrinkled seeds D
100 round seeds
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62What is a source of genetic variation? A
mutation B adaptation C replication D
transcription
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63In Mendels experiments with a single trait, the
trait that disappeared in the first
generation and reappeared in the next generation
is called the
A homozygous trait B dominant trait C recessive
trait D heterozygous trait
63