Class 10 Biology_Unit 1_Genetics of Life_Simplified Class Notes by Rasheed Odakkal
Class 10 Biology_Unit 1_Genetics of Life_Simplified Class Notes by Rasheed Odakkal
1. Genetics of Life
- Gene, DNA, Nucleotide, Chromosome.
- Protein synthesis of gene and role of RNA.
- Monohybrid-Dihybrid crosses, Laws of Inheritance
- Non-Mendelian Inheritance.
- Variations: Crossing over & Mutation.
Unit Summary:
Heredity and some variations in offspring occur through genes received from their parents.
Genetics is the branch of science that deals with genes, heredity, and variation. Gregor Johann Mendel is known
as the father of genetics because of his hybridization experiments on Pisum sativum, and made some
inferences, which made the foundation of genetics.
Genes located in the DNA molecule, inside the chromosome, in cell nucleus. A gene is a
specific sequence of nucleotides in DNA (Deoxyribo nucleic acid). Proteins, which are synthesised
in ribosomes, according to the instructions of genes, are responsible for the formation of
characteristic features and for controlling metabolic activities.
DNA and histone proteins are the primary components of a chromosome. Chromatids are the
parts of a chromosome which are connected by means of centromere. There are 23 pairs of
chromosomes in the nucleus of each human cell. Of these, 22 pairs are somatic chromosomes,
which control physical characteristics, and one pair is sex-determining chromosome. The genetic
constitution of a female is 44+XX, and that of a male is 44+XY.
Nucleotides are the basic building blocks of DNA. Each nucleotide is composed of a
deoxyribose sugar, a phosphate group, and a nitrogen base. DNA contains the nitrogen bases
adenine, thymine, guanine and cytosine. DNA, which is a double-stranded, helical structure,
contains adenine paired with thymine and guanine paired with cytosine. James Watson, Francis
Crick, and Maurice Wilkins were awarded the Nobel Prize in 1962 for their contributions on the
discovery of the double helix model of DNA.
Cells also containsanother nuceic acid, RNA (Ribonucleic Acid). Most of the RNA are single-
stranded and consist of nucleotides, made up of ribose sugar, phosphate group, and nitrogen bases
such as adenine, uracil, guanine, and cytosine.
Different types of RNA are involved in the protein synthesis of DNA. Transcription, the first stage of
protein synthesis, is the formation of mRNA, from a specific nucleotide sequence (gene) in DNA,
with the help of various enzymes. When this mRNA reaches the ribosome, tRNAs transfer specific
amino acids to the ribosome according to its message. The rRNAs in the ribosome join the amino
acids together to form proteins. This process is called translation. Thes proteins are responsible for
the formation of characteristic features and for controlling metabolic activities.
Through his experiments on pea plants, such as monohybrid crosses and dihybrid crosses,
Gregor Mendel discovered that certain factors are passed from parents to offspring through their
gametes. These factors were later discovered to be genes.
One of the two forms (alleles) of a gene, inherited from parents to offspring is expressed.
According to the dominant allele, the observable characteristics of an organism are called
phenotype and the genetic constitution responsible for these characteristics are called genotype.
When Gregor Mendel conducted hybridisation experiments in pea plants considering the
opposite traits (tallness and dwarfness) of one character (ie,height), the phenotype of all the
offspring in the first generation (F 1) was taller. When this generation was self-pollinated, the second
generation (F2) produced tall and short offspring in a ratio of approximately 3:1. Through this type of
monohybrid cross, Mendel arrived at some conclusions.
- A trait is controlled by two factors.
- When a pair of contrasting traits is subjected to hybridisation, only one of the contrasting
traits is expressed (dominant trait) in the offspring of the first generation and the other
remains hidden (recessive trait). The trait hidden in the first generation reappears in the
second generation.
- When gametes are formed, the factors that determine trait gets separated without mixing.
- The ratio of dominant to recessive traits in the offspring of the second generation is 3:1.
When dihybrid crosses were performed on plants with two pairs of contrasting traits of the
same plant such as height of the plant and shape of seed, the same phenotype was obtained in the
first generation (F1). When these were self-pollinated to produce the second generation (F 2),
phenotypes different from the parent plants were obtained. The offspring were obtained in a ratio of
approximately 9:3:3:1. The hypothesis that Mendel arrived at through such dihybrid crosses is given
below.
- When two or more different traits are combined, each trait is inherited independently to the
next generation without mixing each other.
In 1865, Gregor Mendel presented his conclusions to the scientific world, but they were
ignroed. Later, in 1900, Hugo de Vries, Carl Correns and Erich Von Schermak recognized the
importance of Mendel's Laws of Inheritance and since then Mendel became known as the father of
genetics.
Some later studies have revealed some limitations to Mendel's laws, which is known as
Non-Mendelian Inheritance. (Examples include incomplete dominance, codominance, multiple
allelism, and polygenic inheritance.and polygenic inheritance.).
It is now possible to alter the characteristics of organisms through gene editing, which makes
desirable changes to certain genes in DNA. Jennifer A. Doudna and Emmanuel Carpentier were
awarded the 2020 Nobel Prize in Chemistry for developing the CRISPR-Cas9 technology for gene
editing.
Variations are characters expressed in offspring, that differ from their parents. The genetic
processes that cause variations are crossing over, which occurs in the first stage of meiosis, and
mutation, which is the sudden heritable change in the genetic structure. Mutations play a crucial role
in the process of evolution.
Questions and Answers:
1. What is gene editing? Name a technology used for gene-editing? Who were introduced this
technology?
Gene editing is the process of making desired changes to certain genes in DNA.
CRISPR-Cas9 is a technology used for gene-editing. Jennifer A. Doudna and Emmanuel
Carpentier introduced this technology.
(They were awarded the 2020 Nobel Prize in Chemistry for this).
2. What are the benefits of gene editing?
Gene editing is expected to make revolutionary advances in genetic disease therapy, treatment of
cancer and in the production of disease and pest resistant varieties of crops or vaccines.
3. What is a gene? Where is this located?
A gene is a specific sequence of nucleotides in DNA (Deoxyribo nucleic acid). Proteins, which are
synthesised according to the instructions of genes, are responsible for the formation of
characteristic features and for controlling metabolic activities. Genes are located in the DNA
molecule, inside the chromosome.
4. Who proposed the double helical model of DNA? What helped them discover this structure?
James Watson and Francis Crick.
They were able to derive the double helix model from DNA X-ray diffraction studies of Rosalind
Franklin and Maurice Wilkins, especially from the ‘Photo 51’ taken by Rosalind Franklin.
(James Watson, Francis Crick and Maurice Wilkins were awarded the Nobel Prize in Medicine in
1962.)
5. What are nucleotides? Name the components of a nucleotide?
Nucleotides are the basic structural units of DNA and RNA. A nucleotide is composed of a 5
carbon sugar, a phosphate group, and a nitrogen base.
phosphate
Nitrogen base
Sugar
Peculiarity Reason
1. Incomplete Pink coloured flower appears when The dominant allele cannot fully hide
dominance a red flowered 4 o'clock plant is the allele of the recessive trait.
hybridised with a white flowered one
2. Roan coat pattern, found on some Both alleles exhibit their traits at the
Co-dominance cattle and horses. same time.
3. Multiple ABO blood group in humans More than two alleles (IA, IB, i alleles)
Alleles determine the blood group.
4. Polygenic Difference in skin colour. More than one gene controls the
Inheritance production of melanin.
31. Why are traits (variations) different from those of parents seen in offspring?
Processes like crossing over and mutation.
32. What is crosssing over? How does this cause variation?
During the first phase of meiosis, pairing of homologous chromosomes occur
and chromatids at the chiasma region exchange the broken segments each chiasma
other. This exchange is known as crossing over.
Through this exchange of genes, a recombination of alleles occur resulting
the appearance of new traits in offspring.