Inheritance and Variation
Inheritance and Variation
Inheritance and Variation
THIRU
KARTHICK
CLASS: 12-C
SUBJECT: BIOLOGY
TOPIC: INHERITANCE AND
VARIATION
Contents
INTRODUCTION:..........................................................................................................................................3
VARIATION:.................................................................................................................................................3
Law of Dominance:..............................................................................................................................5
Law of Segregation:.............................................................................................................................6
INCOMPLETE DOMINANCE:.....................................................................................................................6
CO-DOMINANCE:.....................................................................................................................................7
SEX DETERMINATION:.................................................................................................................................9
MUTATION:...............................................................................................................................................10
GENETIC DISORDERS:................................................................................................................................10
1) Mendelian disorders:.........................................................................................................................11
2) Chromosomal disorders:...................................................................................................................11
CONCLUSION:............................................................................................................................................12
BIBLIOGRAPHY:..........................................................................................................................................12
INTRODUCTION:
An elephant gives birth to only an elephant baby, a mango seed only gives rise to a
mango tree, human beings give birth to only young human beings. This kind of continuation of
species by giving birth to individuals with similar heredity or traits is because of inheritance.
Thus, heredity is a process of transmitting heritable traits to young ones by their parents. This
transfer can be conducted through either asexual reproduction or sexual reproduction. The traits
that continue the legacy are found in genes on the chromosomes within the body of an
individual. Genes are the carriers of instructions that could have a similarity to one of their two
parents.
VARIATION:
genetic recombination, crossing over, environmental changes, and other such ways lead to
genetic variation. It is the impact of these on the way genes are expressed.
MENDEL’S LAW OF INHERITANCE:
pea in the back of his garden to establish the principle of heredity. For this, he took 14 true-
breeding pea plants with seven distinguishable characters that had two opposite traits. Mendel
called genes “factors” that pass to the offspring from the parents. And the factors (genes) that
gene (one pair of alleles) controlling a single character. It is also called monohybrid cross or
monogenic inheritance. Mendel conducted experiments of plant hybridization on garden pea (Pisum
sativum). His experiments showed the segregation of a single gene during inheritance. One of his
experiments is with tallness and dwarfness. He crossed a true breeding tall plant with a true breeding
dwarf plant. In the F1 generation, all the off springs were tall. This indicated that tallness is dominant over
dwarf-ness. When he allowed two F1 plants to self-pollinate, both tall and dwarf plants were found in the
i) Law of Dominance
ii)Law of Segregation
Law of Dominance:
is dominant. And, the dominant allele is expressed in the phenotype. So, when homozygous tall
with (TT) alleles are crossed with dwarf (tt) plants, all the resulting offspring plants are tall and
So, the characters are passed to gametes without blending. Also, heterozygotes produce different
Incomplete Dominance:
allele for a specific trait is not completely expressed over its paired allele. This results in a third
phenotype in which the expressed physical trait is a combination of the dominant and recessive
white snapdragon plants. For example, when a plant which is homozygous for red flowers (AA)
is crossed with a plant which is homozygous for white flowers (aa), the plants of the
F1 generation produce pink flowers which is a blend of red and white condition. This result
clearly indicates that neither red flowered condition nor white flowered condition is dominant.
However, when two hybrid plants with pink flowers (Aa) are crossed, the F2 generation plants
show red flowered, pink flowered and white flowered in the ratio 1:2:1.
Co-dominance:
in a heterozygous condition are fully expressed. This results in offspring with a phenotype that is
neither dominant nor recessive. A typical example showing co-dominance is the ABO blood
group system. For instance, a person having A allele and B allele will have a blood type AB
because both the A and B alleles are codominant with each other. Here neither of the two A or B
each trait. One parent carries homozygous dominant allele, while the other one carries
homozygous recessive allele. The offsprings produced after the crosses in the F1 generation are
all heterozygous for specific traits. One of the experiment Mendel did was with colour and the
shape of seeds at a time. He picked the wrinkled-green seed and round-yellow seed and crossed
them. He obtained only round-yellow seeds in the F1 generation. This indicated that round shape
and yellow colour of seeds are dominant in nature. Meanwhile, the wrinkled shape and green
colour of seeds are recessive traits. Then, F1 progeny was self-pollinated. This resulted in four
the observations he made on dihybrid crosses which are known as Mendel’s Law of Independent
Assortment. This particular law of Mendel states that “when two pairs of traits are combined in a
hybrid, segregation of one pair of characters is independent of the other pair of characters”. In
simple words, this law explains the independent separation of genes. It means that alleles
inherited by progeny from different traits are acquired independently. A simple way to
understand this law is with the help of a Punette square when carried out with two pairs of genes
during the stage of meiosis and egg-production and pollen in the F1 generation of the RrYy
plant.
SEX DETERMINATION:
different organisms. Henking first observed X chromosome and named it X body. The
chromosomes that determine the development of sexual characters are known as sex
chromosomes and the rest of the chromosomes are known as autosomes. When the male
produces two different kinds of gamete, it is known as male heterogamety.When the female
is inherited from either parent and denoted as XX. Males in humans have 1X and 1Y
chromosome, where the X is inherited from the mother and the Y from the father. So, we can say
that it is the father who determines the sex of the child. At the time of spermatogenesis in males,
both types of gametes are produced- one carrying the X chromosome and one carrying the Y. At
the time of fertilization, the sex of the resulting zygote will depend on which gamete of the father
will fuse with the X of the mother. We can, therefore, say that there is a 50% chance that the
results in the changes in the phenotype and genotype of an entity. The mutation also brings
variations in DNA along with the recombination. The chromosomal alteration has its negative
effects and causes aberrations or abnormalities. These aberrations or abnormalities are usually
observed in the cancer cells, according to the studies. Another type of mutation that takes place
as a result of changes in a single base pair of DN is called a point mutation. For example,
insertions and deletions of base pairs of DNA along with sickle cell anaemia leads to frameshift
mutations.
GENETIC DISORDERS:
There are many disorders in the human being that are inherited and
studying the inheritance pattern of a particular trait present in various generations of individual.
1) Mendelian disorders:
Colour blindness
Cystic fibrosis
Thalassemia
Phenylketonuria
Sickle cell anaemia
Haemophilia
2) Chromosomal disorders:
(i) Aneuploidy- Gain or loss of one or more chromosomes. It is due to failure of segregation of
(ii) Polyploidy- It is often found in plants. This happens due to an increase in the full set of
Mendel has given laws for inheritance of one gene and inheritance of two genes. Inheritance for
one gene has 2 laws namely law of dominance and law of segregation. Mendel has given the law
of independent assortment for inheritance of two genes. Incomplete dominance and Co-
dominance are other related concepts discussed here. Sex determination in humans have 50%
chance to be a male and 50% chance to be a female depending upon the gamete which enters.
mutation, genetic disorders and types of genetic disorders are all given above.
Bibliography:
ncert.nic.in
studycbse.in
www.vedantu.com
www.learncbse.in