Title: Genetics: Mendel and Beyond
1Genetics Mendel and Beyond
2Genetics Mendel and Beyond
- By the end of this chapter you should be able to
- Describe Mendels Experiments and the Laws of
Inheritance - Predict inheritance patterns of monohybrid and
dihybrid crosses using a punnett square - Explain examples of gene interactions
- Distinguish between genes and chromosomes
- Explain sex determination and
- Predict sex-linked inheritance
3The Foundations of Genetics
- Applied genetics (plant and animal breeding) has
been used for five thousand years ago or more. - The foundation for the science of genetics is
credited to Gregor Mendel who used varieties of
peas to conduct experiments on inheritance. - Mendels research was ignored until the turn of
the twentieth century. - Meiosis provides an explanation for Mendels
theory.
4The Foundations of Genetics
- Plants have some desirable characteristics for
genetic studies - They can be grown in large quantities.
- They produce large numbers of offspring.
- They have relatively short generation times.
- Many have both male and female reproductive
organs, making self-fertilization possible. - It is easy to control which individuals mate.
5Figure 10.1 A Controlled Cross between Two
Plants
6Mendels Experiments and the Laws of Inheritance
- Mendel looked for characters that had
well-defined alternative traits and that were
true- breeding. - Mendel developed true-breeding strains to be used
as the parental generation, designated P. - The offspring from the cross of the P parents are
called the first filial generation, designated
F1. - When F1 individuals are crossed to each other or
self-fertilized, their progeny are designated F2.
7Mendels Experiments and the Laws of Inheritance
- Mendels experiment 1
- A monohybrid cross involves one character (seed
shape) and different traits (spherical or
wrinkled). - SS x ss ? Ss
- The F1 seeds were all spherical the wrinkled
trait failed to appear at all. - Because the spherical trait completely masks the
wrinkled trait when true-breeding plants are
crossed, the spherical trait is considered
dominant and the wrinkled trait recessive. We
represent the dominant trait with a capital
letter and the recessive trait with a small case
letter.
8Mendels Experiments and the Laws of Inheritance
- Mendels experiment 1 continued
- The F1 generation was allowed to self-pollinate
to produce F2 seeds. - Ss x Ss ? 3Ss, 1 ss
- 3 are heterozyous smooth and 1 is homozygous
wrinked. - In the F2 generation, the ratio of spherical
seeds to wrinkled seeds was 31.
9Figure 10. 3 Mendels Experiment 1 (Part 1)
10Figure 10. 3 Mendels Experiment 1 (Part 2)
11Mendels Experiments and the Laws of Inheritance
- From these results, Mendel reached several
conclusions - The units responsible for inheritance are
discrete particles that exist in pairs and
separate during gamete formation this is called
the particulate theory. - Each pea has two units of inheritance for each
character. - During production of gametes, only one of the
pair for a given character passes to the gamete. - When fertilization occurs, the zygote gets one
unit from each parent, restoring the pair.
12Mendels Experiments and the Laws of Inheritance
- Mendels units of inheritance are called genes (a
portion of the chromosomal DNA that resides at a
specific locus and codes for a particular
function) different forms of a gene are called
alleles. - True-breeding individuals have two copies of the
same allele (i.e., they are homozygous). - Some smooth-seeded plants are Ss or heterozygous.
- The physical appearance of an organism is its
phenotype (what it looks like) the actual
composition of the organisms alleles for a gene
is its genotype. Homozygous dominant
heterozygous dominant homozygous recessive
13- An organisms trait does not always reveal its
genetic composition. Why? - Heterozygous genotypes yield phenotypes showing
the dominant trait. - The same phenotype can result from different
genotypes.
14Mendels Experiments and the Laws of Inheritance
- Mendels first law is called the law of
segregation The two alleles of a trait segregate
(separate) during meiosis. - Each gamete receives one member of a pair of
alleles. - Determination of possible allelic combinations
can be accomplished by a Punnett square.
15Punnett Square
- Another way to demonstrate this is through the
use of a punnett square - S S S s
- s Ss Ss S SS Ss
-
- s Ss Ss s Ss ss
- Since one character with two contrasting traits
are being crossed, this is called a monohybrid
cross
16Figure 10.4 Mendels Explanation of Experiment 1
17Figure 10.5 Meiosis Accounts for the Segregation
of Alleles (Part 1)
18Figure 10.5 Meiosis Accounts for the Segregation
of Alleles (Part 2)
19Mendels Experiments and Laws of Inheritance
- How do we determine if a purple flowering plant
is SS or Ss? - We could cross the purple flowering plant of
unknown genotype with a true breeding purple
flowering plant or a white flowering plant - SS x SS (unknown) or SS x Ss (unknown)
- all spherical all spherical
- ss x SS (unknown) or ss x Ss (unknown)
- all spherical 2 spherical 2 wrinkled
20Mendels Experiments and the Laws of Inheritance
- Crossing an unknown with a homozygous recessive
is called a test cross. - An individual with a dominant trait is crossed
with a true-breeding recessive (homozygous
recessive). - The appearance of the recessive phenotype in half
the offspring indicates that the parent is
heterozygous.
21Figure 10.6 Homozygous or Heterozygous?
22Mendels Experiments and the Laws of Inheritance
- Mendels second law, the law of independent
assortment, states that alleles of different
genes assort into gametes independently. - This can be shown by using a dihybrid crosses.
- For example, in pea plants purple flowers are
dominant over white flowers and green pods are
dominant over yellow pods. - Cross a purebreeding purple flowering plant with
green pods with a white flowering plant with
yellow pods. - Random fertilization of gametes results in all
heterozygous offspring. -
23Dihybrid Crosses
- PPGG x ppgg PpGg
- If we allow these plants to self-pollinate, PpGg
x PpGg, what are the possible offspring? - Each parent could produce four different gametes
PG, Pg, pG, or pg
24Dihybrid Crosses
25Dihybrid Crosses
- PG Pg pG pg
- PG PPGG PPGg PpGG PpGg
- Pg PPGg PPgg PpGg Ppgg
- pG PpGG PpGg ppGG ppGg
- pg PpGg Ppgg ppGg ppgg
- Putting these into a punnett square results in a
9331 ratio
26Figure 10.7 Independent Assortment
27Mendels Experiments and the Laws of Inheritance
- Humans cannot be studied using planned crosses.
- Therefore, human geneticists rely on pedigrees.
- Human pedigrees do not show clear proportions.
- Outcomes for small samples fail to follow the
expected outcomes closely.
28Mendels Experiments and the Laws of Inheritance
- If neither parent has a given phenotype, but it
shows up in their offspring, the trait is
recessive and the parents are heterozygous. - Half of the children from such a cross will be
carriers (heterozygous for the trait). - The chance of any one childs getting the trait
is 1/4.
29Figure 10.11 Recessive Inheritance
30Mendels Experiments and the Laws of Inheritance
- A pedigree analysis of the dominant allele for
Huntingtons disease shows that - Every affected person has an affected parent.
- About half of the offspring of an affected person
are also affected (assuming only one parent is
affected). - The phenotype occurs equally in both sexes.
31Figure 10.10 Pedigree Analysis and Dominant
Inheritance
32Polydactyl
33Figure 10.11
figure 10-11.jpg
34Albinism
35Huntingtons Disease
36Marfans
37Marfans
38Alleles and Their Interactions
- Differences in alleles of genes consist of slight
differences in the DNA sequence at the same
locus, resulting in slightly different protein
products. - This is a mutation. Alleles can mutate randomly.
39Alleles and Their Interactions
- A population can have more than two alleles for a
given gene. - In rabbits, coat color is determined by one gene
with four different alleles. Five different
colors result from the combinations of these
alleles. - Even if more than two alleles exist in a
population, any individual can have no more than
two of them one from the mother and one from the
father. - Also send in ABO blood typing.
40Figure 10.12 Inheritance of Coat Color in Rabbits
41Alleles and Their Interactions
- A white snapdragon crossed with a red snapdragon,
gives an intermediate phenotype pink - Incomplete Dominance
- In the case of snapdragons, one allele codes for
an enzyme that leads to the formation of red
pigment. The other allele does not code for
pigment production.
42Figure 10.13 Incomplete Dominance Follows
Mendels Laws
43- The F2 offspring, however, demonstrate Mendelian
genetics. For self-fertilizing F1 pink flowers
the F2 progeny have a phenotypic ratio of 1
red2 pink1 white. - Other examples include roan cattle and blue
Andalusian chickens - Tay Sachs Disease is also an example of
incomplete dominance.
44Incomplete Dominance
- Persons with Tay Sachs lack a crucial enzyme to
metabolize a type of lipid. The lipids
accumulate in the brain interfering with normal
function. Causes regression of nervous system, -
blind, deaf, bedridden, inability to move limbs - Cherry red spot in retina is one indication
- Heterozygotes have an intermediate level of the
lipid metabolizing enzyme
45Tay Sachs
46Tay Sachs
47Alleles and Their Interactions
- In codominance, the two different alleles are
both expressed in the heterozygotes. - In the human ABO blood group system the alleles
for blood type are IA, IB, and IO. We inherit
two of these three alleles. - Two IA, or IA and IO, results in type A.
- Two IB, or IB and IO, results in type B.
- Two IO results in type O.
- IA and IB results in type AB. The alleles are
called codominant.
48Figure 10.14 ABO Blood Reactions Are Important
in Transfusions
49ABO Genetic Problems
- A couple have their blood typed before marriage.
They both are AB. What types of blood might
their children have? Explain - A woman sues a man for child support. She has
type A blood, her child type O, and the man type
B. Could the man be the father? Why or why not?
50ABO Genetic Problems
- A wealthy, elderly couple die together in a car
accident. Soon a young man shows up to claim
their fortune, contending that he is their only
son who ran away from home when he was a young
man. Other relative dispute his claim. Hospital
records show that the deceased couple were blood
types AB and O. The claimant is type O. Do you
think the claimant is an impostor? Explain.
51Pleiotropic alleles
- Most genes have multiple phenotypic effects.
- An example is the coloration pattern and crossed
eyes of Siamese cats, which are both caused by
the same allele. - These unrelated characters are caused by the same
protein produced by the same allele. - Another example is sickle cell anemia.
52Sickle Cell Anemia
53Gene Interactions
- In epistasis a gene at one locus alters the
phenotypic expression of a gene at a second
locus. - An example is coat color in mice
- The B allele produces a banded pattern, called
agouti. The b results in unbanded hairs. - The genotypes BB or Bb are agouti or banded. The
genotype bb is black. - Another locus determines if any coloration
occurs. The genotypes AA and Aa have color and aa
are albino. - Cross two AaBb mice. What is the phenotype?
54Figure 10.15 Genes May Interact Epistatically
55Gene Interactions
- When two homozygous strains of plants or animals
are crossed, the offspring are often
phenotypically stronger, larger, and more
vigorous than either parent. - This phenomenon is called hybrid vigor.
Hybridization is now a common agricultural
practice used to increase production in plants.
56Figure 10.16 Hybrid Vigor in Corn
57The Environment Affects Gene Action
- Genotype and environment interact to determine
the phenotype - Environmental variables such as light,
temperature, and nutrition can affect the
translation of genotype into a phenotype - Examples Siamese cats, hydrangea flowers
- Twin Studies
58Genes and Chromosomes
- Homologous chromosomes can exchange corresponding
segments during prophase I of meiosis (crossing
over). - Genes that are close together tend to stay
together. - The farther apart on the same chromosome genes
are, the more likely they are to separate during
recombination.
59Figure 10.19 Crossing Over Results in Genetic
Recombination
60Sex Determination in Humans
- Sex chromosomes carry genes that determine
whether male or female gametes are produced. - In humans, the Y chromosome has a sex-determining
region - SRY - The SRY gene codes for a functional protein. If
this protein is present, testes develop if not,
ovaries develop. - Some XY individuals lacking a small portion of
the Y chromosome are phenotypically female. - Some XX individuals with a small piece of the Y
chromosome are male.
61Sex linked traits
- The Y chromosome carries few genes (20). The X
chromosome carries many genes. This difference
generates a special type of inheritance called
sex-linked inheritance - Two well-know traits carried on the X chromosome
are colorblindness and hemophilia. - Sex linked traits tend to be expressed with
greater frequency in males. - Can you explain why?
- This is due to the fact that many of these
diseases are only on the X chromosome and not the
Y
62Hemophilia
63Colorblindness
64Figure 10.24 Red-Green Color Blindness Is a
Sex-Linked Trait in Humans
65Sex Determination and Sex-Linked Inheritance
- Pedigree analysis of X-linked recessive
phenotypes - The phenotype appears much more often in males
than in females. - A male with the mutation can pass it only to his
daughters. - Daughters who receive one mutant X are
heterozygous carriers. - The mutant phenotype can skip a generation if the
mutation is passed from a male to his daughter
and then to her son.
66Sex Determination and Sex-Linked Inheritance
- Disorders can arise from abnormal sex chromosome
constitutions. - Turner syndrome is characterized by the XO
condition and results in females who physically
are slightly abnormal but mentally normal and
usually sterile. - The XXY condition, Klinefelter syndrome, results
in males who are taller than average and always
sterile.
67Non-Nuclear Inheritance
- Mitochondria, chloroplasts, and other plastids
possess a small amount of DNA. - Some of these genes are important for organelle
assembly and function. - Mitochondria and plastids are passed on by the
mother only, as the egg contains abundant
cytoplasm and organelles. - A cell is highly polyploid for organelle genes.
- Organelle genes tend to mutate at a faster rate.