Mendel and Heredity
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Transcript Mendel and Heredity
Mendel and Heredity
Chapter 8
8.1 The Origins of Genetics
Heredity is the passing
of characters from
parents to offspring
Used throughout history
to alter crops and
domestic animals
Gregor Johann Mendel –
Austrian Monk
Used pea plants and bred
different varieties
Developed rules to
accurately predict
patterns of heredity
Why Peas?
2 characters have clearly different
forms
Male and female reproductive
parts are in same flower
Character = inherited characteristic
(color)
Trait = single form of character
(purple)
Can control fertilization
Flower can fertilize itself (selffertilization) or can cross pollen from 1
plant to another (cross-pollination)
Peas are small, grow easily,
mature quickly, and produces
many seeds so results obtained
quickly
Traits Expressed as Simple Ratios
Mendel started by looking at 1 characteristic
(monohybrid), such as color, with 1 pair of
contrasting traits, purple or white flowers
Only allowed plants to self-pollinate for many
generations
True-breeding – all offspring show only 1 trait
Parental (P) generation
Cross pollinated 2 P generation plants with
contrasting traits
Offspring called filial (F1) generation
Counted numbers of each trait
Allowed F1 generation to self pollinate
Offspring called F2 generation
Each characterized and counted
Mendel’s Results
F1 showed only 1 form of character other had
disappeared
When F1 self pollinates other trait reappears in
some of F2
Found ratio of traits to be 3 to 1
3 white flowers to 1 purple flower
Same ratio found for any trait he studied
8.2 Mendel’s Theory
We used to think offspring were blend of
traits
Tall x short = medium
Mendel’s experiments showed us this is
not entirely true
Mendel’s Hypothesis
There are 2 copies of a gene, one from each
parent, for each inherited characteristic
There are different versions of genes called
“alleles”
Tall or short
When both versions are present one may be
dominant (completely expressed) and the other
may be recessive (not expressed when
dominant is present)
When you form gametes, alleles separate
independently so only one allele in each gamete
Mendel’s Finding in Modern Terms
Use letters to show alleles
Capitol = dominant (T, P, Y, etc…)
Lower case = recessive (t, p, y, etc…)
Homozygous = letters are same
Homozygous
dominant = TT, PP
Homozygous recessive = tt, pp
Heterozygous = letters are different
Tt,
Pp
Only dominant allele is expressed
Genotype = set of alleles
What you actually have
TT, Tt, or tt
Phenotype = what is expressed
How it looks
Tall, Tall, or Short
Mendel’s Laws of Heredity
Law of Segregation
2 alleles for a character segregate when gametes are
formed
Behavior of chromosomes during meiosis
Law of Independent Assortment
1 character does not affect another
Alleles of different genes separate independently of
on another
Now know this only applies to genes located on
different chromosomes or that are far apart on same
chromosome
8.3 Studying Heredity:
Punnett Squares
Breeders want
certain
characteristics
when they breed
(cross) animals
Horticulturists
produce plants
with specific
characteristics
Punnett Square
Used to predict
outcomes
Shows all
possible
combinations of
gametes
Put 1st parents
genotype on top
Put 2nd parents
genotype on side
Do the cross
TT
Tt
Tt
tt
• So in Mendel’s F1
generation, a pure Tall
plant bred with a pure
short plant can only
give 1 kind of offspring
due to dominance of
tall allele
Determining Unknown Genotypes
How do you know if a tall plant is
homozygous or heterozygous? They both
look tall
Can do a Test Cross
If dominant phenotype is shown with unknown
genotype, cross it with homozygous recessive
Test Cross Results
If unknown is
homozygous
dominant, all
offspring of test
cross will have
dominant trait
Test Cross Results
If unknown is
heterozygous,
offspring of test
cross will have 2
dominant and 2
recessive
phenotypes
Can use probability calculations to predict
results of genetic crosses
Probability is the likelihood a specific event
will occur
Probability = # of 1 kind of possible
outcome divided by total number of
possible outcomes
We will express these as fractions
Chance a coin will come up heads
1 head / 2 sides = ½
DD = ¼
Dd = 2/4 or ½
dd = ¼
Dihybrid Cross
Uses a Punnett Square to determine
outcomes of 2 traits at one time
Example: Surface and Color
Surface:
Color:
RR, Rr, or rr
YY, Yy, yy
round or wrinkled
yellow or green
What are the possible combinations?
RY, Ry, rY, ry
So if you have 2 purebred homozygous
parents RRYY and rryy and you mate
them, what do you get?
All offspring will be RrYy
What if you have F1 breed?
Make a Punnett Square of possible gametes
for each parent
What possible combos can parents offer?
Do
you remember FOIL?
RY, Ry, rY, ry
You never have to count the results
of a dihybrid cross between
heterozygotes!
9 with both dominant traits
3 with first dominant and second recessive
3 with first recessive and second dominant
1 with both recessive traits
So 9:3:3:1
Inheritance of Traits
Pedigree
Family history that shows how a trait is inherited over
several generations
Helpful in tracking genetic disorders
Carrier – have allele for trait but show no
symptoms
Things You Can Find From A Pedigree
Autosomal or SexLinked?
If autosomal it will
be equal in both
sexes
If sex linked
generally only
found in males
Y
linked
X
Hairy ear rims
linked
Color-blindness
Hemophilia
Dominant or recessive
Autosomal Dominant –
every individual with
condition will have parent
with condition
Achondroplasia – type of
dwarfism
Huntington’s Disease –
brain degenerates
Autosomal Recessive – 1,
2, or no parents with
condition
Cystic fibrosis
Sickle cell anemia
Albinism
Heterozygous or
Homozygous
Autosomal
homozygous dominant
or heterozygous
phenotype will show
dominant allele
Homozygous
recessive will show
recessive allele
2 heterozygous of
recessive allele don’t
show condition but can
have children that do
8.4 Complex Patterns of Heredity
Complex Control
Most of the time characters display much
more complex patterns than simple dominantrecessive patterns
Characters can be influenced by several
genes
Polygenic Inheritance
Several genes affect a character
These genes may be scattered along same
chromosome or on different chromosomes
Determining the effect of any one gene is difficult
Crossing over and independent assortment
create many different offspring combos
Eye color, height, weight, hair, intelligence, and
skin color
Usually gives a range of expression
Polygenic Inheritance
Intermediate Characters
Incomplete dominance
Phenotype that is intermediate between 2 parents,
neither is completely dominant
White x red = pink
Straight hair x curly hair = wavy hair
Multiple Alleles
Characters controlled by genes with 3+
alleles
Humans have ABO blood types
IA, IB, i
Letters A and B refer to carbohydrates on
surface of red blood cells
i has neither carbohydrate
IA and IB are dominant over I, but not over
each other (codominant)
Still only 2 possibilities in a person
Blood Types
2 forms are displayed
at the same time
Codominance – both
expressed, not
blended
IAIB both expressed
ii = Type O
Characters Influenced by Environment
Plants may change color
based on pH of soil
Arctic fox
Siamese cats
Summer – enzymes produce
pigments for darker fur
Winter – no enzymes, no
pigments to darken fur
Dark fur in cooler parts
Humans
Height related to nutrition
Skin color based on sun
exposure
Twins are genetically identical,
any difference is due to
environment
Genetic Disorders
Proteins encoded by genes must function
precisely for normal development and function
Genes may be damaged or copied wrong
causing faulty proteins
Mutation = changes in genetic material
Rare because cells try to correct errors
Harmful effects produced by inherited mutations
Many carried by recessive alleles
Sickle Cell Anemia
Recessive genetic
disorder
Mutated allele produces
defective form of
hemoglobin causing red
blood cells (rbc) to be
misshapen
These rupture easily
causing less O2 to be
carried and may get stuck
and cut off blood supply
Recessive allele protects
heterozygous individuals
from malaria
Parasites in sickle rbc die
Normal rbc still transport
oxygen
Cystic Fibrosis
Most common fatal,
hereditary, recessive
disorder in Caucasions
1 in 25 has at least 1
copy of defective gene
that makes a protein
needed to move chloride
in and out of cells
Mucus clogs organs
1 in 2,500 homozygous
for cystic fibrosis
No cure
Hemophilia
Impairs bloods ability to clot
Sex-linked
Dozen+ genes code for clotting proteins
1 mutation on X chromosome causes
Hemophilia A
Males only get 1 X chromosome
Huntington’s Disease
dominant allele on autosome
1st symptoms - mild forgetfulness and
irritability in 30’s and 40’s
Eventually lose muscle control, spasms,
severe mental illness, and death
Treating Genetic Disorders
Most can’t be cured
Genetic Counseling – tells of possible
genetic problems with offspring, may be
treated if early enough
Phenylketonuria (PKU)
Lack enzyme that converts amino acid
phenylalanine into tyrosine so it builds up
in the body and causes severe mental
retardation
Can be placed on phenylalenic diet
Gene Therapy
Replace defective genes with normal ones
Isolate copy of gene
Put working copy into a virus
Virus infects and puts gene in
Infected cells are cured
Still trying to get this to work