Chapter 4 Heredity
Class 10 Science Notes
Introduction to Heredity
All living things reproduce, creating offspring that resemble their parents. This passing of characteristics from one generation to the next is a fundamental principle of life. The structures responsible for this transmission are the chromosomes found within the nucleus of every cell. During cell division, these chromosomes are copied and passed to the new cells.
While parental characteristics are passed down, variations can occur due to environmental influences and other factors. The specific characteristics of any living being are determined by the number of chromosomes it has and the millions of genes contained within them. The branch of biology dedicated to the study of genes and heredity is known as genetics.
Modern genetics builds on the foundational laws discovered by Gregor Mendel. Today, advanced genetic technologies and engineering allow for artificial reproduction and the development of hybrid organisms.
4.1 Cell Division
Cell division is essential for the growth, development, and repair of organisms.
When an organism reproduces sexually, cells in the reproductive organs undergo a special type of division called meiosis to produce gametes (sperm and egg). When male and female gametes fuse during fertilization, they form a single-celled zygote. This zygote then divides repeatedly through mitosis, eventually developing into a complete, multicellular organism.
All cell division occurs in two main phases:
- Karyokinesis: The division of the cell’s nucleus.
- Cytokinesis: The division of the cytoplasm and cell membrane that follows the division of the nucleus.
A. Mitosis Cell Division (Equational Division)
Mitosis is the process of cell division that occurs in all body cells (somatic cells) except for the reproductive cells. It is responsible for growth, the development of the body, and the repair of tissues.
In this process, a single parent cell divides to form two identical daughter cells. Most cells in the human body are diploid (2n), meaning they contain two sets of chromosomes—one set inherited from the father and one from the mother.
Before mitosis begins, the DNA in the chromosomes replicates, creating two identical copies. As the cell divides, each new daughter cell receives one complete copy. Because the daughter cells have the exact same number of chromosomes as the parent cell, mitosis is also known as equational division.
Significance of Mitosis:
- Physical Growth: It increases the number of cells, allowing the organism to grow.
- Regeneration and Repair: It replaces old or damaged cells in injured areas.
- Asexual Reproduction: It is the method of reproduction for some plants and simple invertebrates.
- Genetic Stability: It ensures that all new cells have the same genetic makeup.
B. Meiosis Cell Division (Reductional Division)
Meiosis is a specialized type of cell division that occurs only in the reproductive organs (testis in males and ovaries in females) to produce gametes.
In this process, one diploid (2n) parent cell divides to form four haploid (n) daughter cells. A haploid cell has half the number of chromosomes as the parent cell. This process occurs in two main phases.
A key event in the first phase of meiosis is crossing over, where genetic material is exchanged between chromosomes. This exchange creates new genetic combinations, which is why offspring from the same parents are not identical. Because the chromosome number is halved in the daughter cells, meiosis is also known as reductional division.
Significance of Meiosis:
- Sexual Reproduction: It produces the gametes necessary for sexual reproduction.
- Genetic Variation: It introduces variation, which is essential for the evolution of species.
- Chromosome Number Maintenance: It ensures that when gametes fuse, the resulting zygote has the correct diploid number of chromosomes.
4.2 Deoxyribonucleic Acid (DNA)
DNA is a long, thread-like molecule found inside cells that carries an organism’s genetic information. In eukaryotic cells (like those in humans, animals, and plants), DNA is located in the chromosomes within the nucleus.
DNA is made of two strands that twist around each other to form a double helix. These strands are built from smaller units called nucleotides. Each nucleotide contains a phosphate, a sugar (deoxyribose), and a nitrogen base.
There are four types of nitrogen bases in DNA:
- Adenine (A)
- Guanine (G)
- Cytosine (C)
- Thymine (T)
These bases pair up in a specific way: Adenine always pairs with Thymine (A-T), and Guanine always pairs with Cytosine (G-C).
4.3 Ribonucleic Acid (RNA)
RNA is another important molecule in the cell. Unlike the double-stranded DNA, RNA is typically single-stranded. It is mainly found in the cytoplasm of the cell.
RNA is also made of nucleotides, but with two key differences from DNA:
- The sugar in RNA is ribose.
- The nitrogen base Thymine (T) is replaced by Uracil (U). In RNA, Adenine (A) pairs with Uracil (U).
There are three main types of RNA:
- Messenger RNA (mRNA)
- Transfer RNA (tRNA)
- Ribosomal RNA (rRNA)
The primary function of RNA is to synthesize proteins based on the instructions encoded in DNA.
4.4 Chromosome
Chromosomes are structures found inside the nucleus of eukaryotic cells. They are made of DNA tightly coiled around proteins called histones.
When a cell is not dividing, the genetic material exists as a tangled network of fibers called chromatin. During cell division, this chromatin condenses to become the visible, distinct structures we know as chromosomes.
Each chromosome consists of two identical arms called sister chromatids, which are joined at a central point called the centromere.
Types of Chromosomes:
Chromosomes are categorized into two types based on their function:
- Somatic Chromosomes (Autosomes): These chromosomes determine the physical characteristics of an individual. In a pair, both somatic chromosomes have the same size and shape.
- Sex Chromosomes: These chromosomes determine the sex of an individual. The two chromosomes in a sex chromosome pair can be different (e.g., X and Y).
Number of Chromosomes:
The number of chromosomes is constant for a particular species.
- Humans have 46 chromosomes (23 pairs).
- Gorillas have 48 chromosomes (24 pairs).
Of the 23 pairs in humans, 22 pairs are autosomes, and one pair consists of sex chromosomes.
Role of Sex Chromosomes in the Determination of Sex in Humans
In humans, sex is determined by the 23rd pair of chromosomes.
- Females have two X chromosomes (XX).
- Males have one X and one Y chromosome (XY).
During meiosis in a female, all the eggs (ova) produced contain one X chromosome (22+X). During meiosis in a male, half the sperm produced contain an X chromosome (22+X), and the other half contain a Y chromosome (22+Y).
Fertilization determines the sex of the offspring:
- If a sperm with an X chromosome fertilizes an egg, the resulting zygote will be XX (a female).
- If a sperm with a Y chromosome fertilizes an egg, the resulting zygote will be XY (a male).
Therefore, there is a 50% probability of having a male or female child.
Sex Determination Chart:
| Father (XY) | ||
|---|---|---|
| Sperm (X) | Sperm (Y) | |
| Mother (XX) | XX (Daughter) | XY (Son) |
| Egg (X) | XX (Daughter) | XY (Son) |
1. Choose the correct option for the given questions.
(a) How many pairs of sex chromosomes are found in the human cell?
(b) What is a chromosome made up of?
(c) What is the main function of sex chromosomes?
(d) What is the smallest unit of the chromosome that helps in the transmission of hereditary characteristics?
(e) Which of the following statements is correct for mitotic cell division?
(f) A technician working in a radiotherapy laboratory was tested after a long time of marriage when there was no childbirth. After the test, it was found that his child production capacity was reduced because he worked in high-intensity radiation for a long time. Which part of the cell is affected in this case?
(g) If there is no DNA transcription in a cell, which process is affected?
(h) If a nucleotide is destructed during DNA replication, what happens to the organism?
(i) Which of the following indicates the set of chromosomes in a cell of a woman?
(j) Which of the following statements is true?
2. Write differences:
(a) Autosome and Sex Chromosome
| Basis of Difference | Autosome | Sex Chromosome |
|---|---|---|
| Function | Determine the physical characteristics and somatic traits of an individual. | Determine the biological sex of an individual. |
| Number in Humans | There are 22 pairs (44 total) in each somatic cell. | There is 1 pair (2 total) in each somatic cell. |
| Homology | The 22 pairs are homologous, meaning each pair has the same size, shape, and gene content. | The pair can be homologous (XX in females) or non-homologous (XY in males). |
| Type Name | Also known as somatic chromosomes. | Also known as heterosomes or allosomes. |
| Presence | Present in both males and females in 22 pairs. | Present as XX in females and XY in males. |
(b) Mitosis and Meiosis
| Basis of Difference | Mitosis | Meiosis |
|---|---|---|
| Cell Type | Occurs in somatic (body) cells. | Occurs in reproductive (germ) cells to form gametes. |
| Number of Divisions | One round of cell division. | Two consecutive rounds of cell division (Meiosis I and Meiosis II). |
| Daughter Cells | Produces two diploid (2n) daughter cells. | Produces four haploid (n) daughter cells. |
| Genetic Makeup | Daughter cells are genetically identical to the parent cell. | Daughter cells are genetically different from the parent cell and each other. |
| Chromosome Number | The chromosome number remains the same as the parent cell (equational division). | The chromosome number is halved in the daughter cells (reductional division). |
| Primary Role | Growth, repair, tissue regeneration, and asexual reproduction. | Production of gametes (sperm and egg) for sexual reproduction. |
(c) DNA and RNA
| Basis of Difference | DNA (Deoxyribonucleic Acid) | RNA (Ribonucleic Acid) |
|---|---|---|
| Sugar | Contains deoxyribose sugar. | Contains ribose sugar. |
| Nitrogenous Bases | Adenine (A), Guanine (G), Cytosine (C), and Thymine (T). | Adenine (A), Guanine (G), Cytosine (C), and Uracil (U). |
| Structure | Typically a double-stranded helix. | Typically single-stranded. |
| Primary Function | Stores and transmits long-term genetic information. | Acts as a messenger carrying instructions from DNA for protein synthesis. |
| Location in Eukaryotes | Primarily found in the nucleus. | Found in the nucleus and cytoplasm. |
(d) Haploid and Diploid
| Basis of Difference | Haploid (n) | Diploid (2n) |
|---|---|---|
| Chromosome Sets | Contains a single set of chromosomes. | Contains two complete sets of chromosomes (one from each parent). |
| Number in Humans | 23 chromosomes. | 46 chromosomes (23 pairs). |
| Cell Type | Found in gametes (sperm and egg cells). | Found in somatic (body) cells. |
| Formation Process | Formed through meiotic cell division. | Formed through mitotic cell division and fusion of gametes (fertilization). |
| Representation | Represented by ‘n’. | Represented by ‘2n’. |
3. Give reason:
(a) Offspring have the same characteristics as their parents.
Offspring inherit characteristics from their parents through the transmission of genes. Genes, which are segments of DNA located on chromosomes, carry the instructions for specific traits. During sexual reproduction, each parent contributes half of their chromosomes (and thus half of their genes) to the offspring, leading to a combination of parental traits.
(b) The male has a main role in the determination of sex.
The determination of sex in humans depends on the sex chromosome contributed by the male’s sperm. A female produces eggs that all contain an X chromosome. A male produces two types of sperm: half with an X chromosome and half with a Y chromosome. If an X-sperm fertilizes the egg, the offspring will be female (XX). If a Y-sperm fertilizes the egg, the offspring will be male (XY). Therefore, the sperm from the male determines the sex.
(c) Though males have both X and Y sex chromosomes, some of them have only male or only female kids.
The sex of each child is an independent event determined by chance. For each pregnancy, there is approximately a 50% probability of the offspring being male and a 50% probability of being female. While statistically unlikely over many births, it is entirely possible for a family to have a sequence of all boys or all girls, just as it is possible to get a series of heads when flipping a coin. It does not mean the male is producing only one type of sperm.
(d) Meiotic cell division is also called reductional cell division.
Meiosis is called reductional division because it reduces the number of chromosomes in the daughter cells to half that of the parent cell. A diploid (2n) parent cell, containing two sets of chromosomes, undergoes division to produce four haploid (n) daughter cells, each with a single set of chromosomes.
(e) Mitotic cell division is also called equational cell division.
Mitosis is called equational division because the number of chromosomes in the daughter cells is equal to that of the parent cell. A diploid (2n) parent cell divides to form two daughter cells that are also diploid (2n), ensuring the chromosome number is maintained across cell generations.
(f) Sexual reproduction is impossible without meiotic cell division.
Sexual reproduction involves the fusion of two specialized sex cells called gametes (sperm and egg) to form a zygote. Meiosis is the essential process that produces these haploid (n) gametes. If gametes were produced by mitosis, they would be diploid (2n), and their fusion would result in a zygote with double the normal number of chromosomes, which is not viable for most species.
(g) Meiotic cell division brings variation.
Meiosis introduces genetic variation in two main ways. First, during a process called “crossing over”, homologous chromosomes exchange genetic material, creating new combinations of genes on each chromosome. Second, the random assortment of these chromosomes into gametes means that each gamete receives a unique mix of parental genes. This variation is fundamental for evolution and the adaptation of species.
4. Answer the following questions:
(a) What is a gene?
A gene is the smallest functional and physical unit of heredity. It is a specific segment of a DNA molecule located on a chromosome that carries the instructions for a particular trait or for making a specific protein.
(b) What is a chromosome? Clarify the role of chromosomes in the body of living beings.
A chromosome is a thread-like structure located inside the nucleus of plant and animal cells, made of protein and a single molecule of DNA.
Role of Chromosomes:
- Hereditary Information: Chromosomes are the carriers of genes, which contain all the hereditary information required for the growth, development, and functioning of an organism.
- Transmission of Traits: They ensure that genetic material is accurately copied and passed on from one generation of cells to the next, and from parents to offspring.
- Sex Determination: A specific pair of chromosomes (sex chromosomes) determines the biological sex of an individual.
(c) Explain the importance of mitotic cell division in the growth and development of the body.
Mitotic cell division is fundamentally important for:
- Growth: A multicellular organism begins as a single cell (a zygote), which undergoes repeated rounds of mitosis to increase the cell count, allowing the organism to grow and develop into its complex form.
- Repair and Regeneration: Mitosis replaces old, worn-out, or damaged cells throughout an organism’s life. For example, it heals wounds by producing new skin cells and constantly replaces blood cells.
- Asexual Reproduction: In some organisms, mitosis is the basis of asexual reproduction, producing offspring that are genetically identical to the parent.
(d) Explain the role of mitosis and meiosis in the reproduction of organisms.
Mitosis: Plays a role in asexual reproduction, where a single parent produces genetically identical offspring. It is also responsible for the growth of a multicellular organism from a single-celled zygote after sexual reproduction has occurred.
Meiosis: Is essential for sexual reproduction. It produces genetically unique haploid gametes (sperm and eggs). The genetic variation it introduces is crucial for the adaptation and evolution of species.
(e) What will happen if meiotic cell division does not occur in the reproductive cell of an organism? Explain.
If meiotic cell division did not occur, sexual reproduction would be impossible. Reproductive cells (gametes) would have to be formed by mitosis, making them diploid (2n). If two diploid gametes fused, the resulting zygote would be tetraploid (4n). With each subsequent generation, the chromosome number would double, leading to genetic instability and non-viable offspring. Therefore, meiosis is necessary to maintain a constant chromosome number across generations in sexually reproducing species.
(f) Clearly explain the role of genes in the transmission of hereditary characteristics in organisms.
Genes act as a blueprint for life. They are specific sequences of DNA that code for proteins, and these proteins in turn determine an organism’s traits (e.g., eye color, height, blood type). During reproduction, genes are packaged into chromosomes and passed from parents to offspring. Each parent contributes a set of genes, and the combination of these genes in the offspring determines its unique set of inherited characteristics.
(g) How is sex determined in humans? Explain with a chart.
In humans, sex is determined by the 23rd pair of chromosomes, the sex chromosomes. Females have two X chromosomes (XX), and males have one X and one Y chromosome (XY). The mother always passes an X chromosome to the child. The father can pass either an X or a Y chromosome. The chromosome from the father’s sperm determines the child’s sex.
Sex Determination Chart:
| Father (Sperm) | |||
|---|---|---|---|
| X | Y | ||
| Mother (Egg) | X | XX (Daughter) | XY (Son) |
| X | XX (Daughter) | XY (Son) | |
• If an X-sperm fertilizes the egg, the result is XX, a daughter.
• If a Y-sperm fertilizes the egg, the result is XY, a son.
(h) A woman is pregnant. What is her probability of giving birth to a daughter? Write in percent.
The probability of giving birth to a daughter is 50%. This is because the father produces sperm containing X and Y chromosomes in roughly equal amounts, so there is a 50% chance of an X-sperm fertilizing the egg to create a female (XX).
(i) A couple gave birth to only a son. Does it mean that the testes of that male produced sperm which have Y-chromosomes only?
No, it does not. The male produces both X-chromosome and Y-chromosome-carrying sperm. The fact that the couple has only had a son is a result of random chance, similar to flipping a coin and getting heads multiple times in a row. For each pregnancy, the probability of having a son remains approximately 50%.
(j) Complete the concept maps ‘a’ and ‘b’. Write the differences between these processes.
A: Reproductive cell → Meiosis cell division → gamete
B: Somatic cell → Mitosis cell division → Two identical daughter cells
Differences between these processes (Mitosis and Meiosis): The differences are the same as those listed in question 2b. The key distinctions are that Meiosis (Process A) occurs in reproductive cells to produce four genetically unique haploid gametes, while Mitosis (Process B) occurs in somatic cells to produce two genetically identical diploid cells for growth and repair.
4.8 Genetics and Genetic Technology
Heredity and Mendelism
All living beings can produce offspring like themselves. Due to this reason, they continue their generation by giving birth to their young ones. Offspring inherit the characters of the previous generations. Although the organisms may look the same, they have some qualities that differ from each other. Parental characteristics are transmitted to the offspring in both sexual and asexual reproduction. These traits are transmitted from one generation to another because of the genes present in the chromosomes of the nucleus of a cell. Each gene carries a specific characteristic of an organism and hence it is responsible for transmitting the qualities of the father and mother to their children.
Gregor Johann Mendel was the first scientist to propose the laws of genetics through various researches. He was born on 22 July 1822 in Austria and is also called the father of genetics. He carried out many experiments on the pea plants grown in his garden to prove that hereditary characters transmit from parents to offspring.
Mendel’s Pea Plant Experiments
While doing experiments, he considered seven pairs of contrasting characters in the pea plant, which are:
- Height of plant: Tall (TT) and dwarf (tt)
- Position of flower: Axial (AA) and terminal (aa)
- Colour of pod: Green (GG) and yellow (gg)
- Shape of pod: Inflated (II) and constricted (ii)
- Shape of seed: Round (RR) and wrinkled (rr)
- Colour of flower: purple (RR) and white (rr)
- Colour of seed: yellow (YY) and green (yy)
Why Mendel Selected Pea Plants:
- Pea plants are bisexual and their flowers are closed, making them naturally self-pollinating plants.
- Cross-pollination can be done if necessary.
- Their life cycle is short, and offspring can be produced faster.
- They have many pairs of contrasting characters.
- Many seeds can be produced at once, and due to this, many offspring can be produced.
- They are easy to cultivate.
Method of Mendel’s Experiment
Mendel studied seven pairs of pure and hybrid traits found in pea plants separately and classified each offspring according to the trait. He selected pure tall pea plants and pure dwarf pea plants and carried out pollination between them to study the heredity. Seeds obtained from that pollination were grown, which were called first filial generation (F1). All the plants of first filial generation were tall. He performed experiments using the remaining pairs of contrasting characters too. He found similar type of results, i.e., only one character was expressed in each of the first filial generations.
Mendel carried out self-pollination between the hybrids produced in first filial generation. After self-pollination, the offspring obtained in the second filial generation (F2) were both tall and dwarf. Among them, 75% were tall and 25% were dwarf.
Results of Mendel’s experiment:
- Tall plants were produced from pure tall plants.
- Tall and dwarf plants were produced in a ratio 3:1 from hybrid tall plants.
- Dwarf plants were produced from pure dwarf plants.
Phenotypic and Genotypic Ratios in Mendel’s Experiment
- Phenotypic ratio is Tall: dwarf = 3:1
- Genotypic ratio is pure tall: hybrid tall: pure dwarf = 1:2:1
Monohybrid Cross and Dihybrid Cross
Laws of Mendel
- Law of dominance
- Law of purity of gametes or law of segregation
- Law of independent assortment
1. Law of Dominance
According to Mendel’s law of dominance, when a cross is made between two pure individuals having a pair of contrasting characters, only one character is expressed externally in F1 generation which is called the dominant character. Hence, the character or trait which is expressed externally in F1 generation is called the dominant character and the character which remains hidden in F1 generation is called the recessive character. In Mendel’s experiment, a cross pollination between pure tall pea plant and pure dwarf pea plant produces all the hybrid offspring in F1 generation in which all are externally tall indicating tall character is dominant and dwarf as a recessive character.
2. Law of Purity of Gametes (Law of Segregation)
Although two different characters coexist in the hybrid of the first generation, they remain pure without losing their originality. In the formation of gametes in the hybrid, during meiosis cell division, the genes of the pure or hybrid allele in the mother cell are separated and only pure characters enter each gamete. It means gametes formed are pure. This law is called the purity of gametes. For example, when self-pollination is performed among the progeny obtained in the first filial generation, the genes of the hybrid alleles separate, and hence tall and dwarf plants are produced in the second generation. The ratio of tall and dwarf plants is 3:1.
Genetic Technology
Currently, the world has advanced a lot in the field of technology, and genetic technology is one of them. This technology helps to develop new qualities by making various changes in DNA easily and quickly. In this technology, modification in the genetic material or gene is carried out.
Nowadays scientists have been able to find out: what genes are, their function, and how they can be altered by adding, deleting, and substituting DNA. Genes are found in all organisms, and they are transferred from one generation to another. Genes have coded instructions that are used to synthesize proteins and to transmit hereditary characters.
Role of DNA Testing in Various Investigations
The use of DNA testing technology has made it easier to investigate various criminal cases and identify the guilty. DNA testing is mostly used for criminal investigations and paternity testing. As a scientific method, it is effective in establishing facts, but DNA testing is a complex and highly sensitive task. Even a simple error can lead to significant inaccuracies. Therefore, to make DNA testing reliable, fair, and effective, special attention is required during the collection and transportation of samples. Samples should also be protected from contamination.
Selective Breeding
Since ancient times, people have been selecting and breeding plants and animals with good qualities for agricultural products they want. The main purpose of selective breeding is to introduce the desired traits in an organism and establish those traits in the future offspring. This method involves selecting and breeding the mother and father, or both, to produce desired plants and animals.
Disadvantages of Selective Breeding
- Usually, selective breeding increases the population of plants and animals having similar genetic traits.
- There is a chance of spreading infectious diseases genetically.
- In this method, breeding between very closely related species is done, so offspring are more likely to suffer congenital genetic problems.
- Selective breeding is also called artificial selection because it involves human interferences.
- Selective breeding inhibits some naturally occurring genetic traits and can affect biodiversity, making it possible for species to become extinct in the future due to some bad traits.
Methods of Selective Breeding
- Inbreeding: Inbreeding is done to establish the population of organisms with predictable traits. In this method, closely related animals are allowed to interbreed.
- Line breeding: It is also a type of inbreeding. In this method, breeding is done between more distant relatives to get animals with desired characteristics.
- Self-pollination: Most plants have both male and female reproductive organs in the same body. They are able to self-pollinate.
- Cross breeding: This method involves breeding two unrelated individuals. Generally, this type of breeding is done between two different species of same genus.
Some Organisms Produced from Cross Breeding
- Liger: The hybrid animal obtained by crossing the male lion and female tiger.
- Tigon: The hybrid animal obtained by crossing the male tiger and female lion.
- Beefalo: A hybrid produced by the cross between a buffalo (American Bison) and a bull.
- Zebroid: The hybrid animal obtained by crossing the zebra and horse.
- Mule: The hybrid animal produced by cross breeding of a donkey and a horse.
- Pomato: The plant produced by crossing potato and tomato.
Artificial Insemination
Nowadays, because of the development of various technologies, fertilization is possible without mating between male and female organisms. The practice of producing offspring of advanced variety has greatly increased nowadays which is by collecting semen from the male located at far distant and inseminating into the body of the female organisms. Offspring produced by this technique are found to be as normal as those produced by natural mating.
Advantages of Artificial Insemination
- There is no need of rearing male for breeding, which saves expenses of rearing.
- It helps to control the infection and spread of disease during mating.
- After collecting semen from the male, it is tested and fertility is checked to ensure the fertility of the male.
- Collected special semen can be used even after the death of the male.
- Collected semen can be easily transported over long distances for fertilization.
In Vitro Fertilization (IVF)
IVF is a method of conception that differs from normal sexual intercourse. The child born through the process of IVF is physically and mentally normal. The characteristics of the child born from IVF may or may not match those of his parents, as this procedure can be done using a couple’s own ovum and sperm, or if a couple has problems with ovum and sperm production, an egg and sperm from a known or unknown donor can also be used.
In IVF, a mature ovum from the ovary of female is taken and stored in a petridish and fused with the sperm of the male in a sophisticated laboratory. The fertilized ovum is then transferred to the female’s womb (uterus) after a few days. It takes about three weeks for a complete cycle. But it may take more time depending upon the nature of the problem. The embryo grows in woman’s uterus as in normal pregnancy.
Advantages of IVF
- IVF is the best method of conception for those couples who are unable to conceive due to various problems related to conception.
- It allows conception by using a couple’s own sperm and ovum or by the use of donor’s sperm and ovum.
- It is more successful than other assisted reproductive techniques.
- It is helpful to solve the problem related to various chromosomal disorders in the child.
1. Choose the correct option for the following questions.
(a) What plant did Mendel use for his experiment?
(b) Which of the following is the genotypic ratio for a Monohybrid cross?
(c) What is the term for a characteristic that is passed down from generation to generation?
(d) A white-skinned child was born to dark-skinned parents. What is the reason for this?
(e) To produce good meat, farmers look for Boer goats and cross them with local goats. What kind of breeding method is this?
(f) Ramit has produced a new plant by crossing an orange plant and a lemon plant. What type of plant is this?
(g) Roshani is a student from the Himalayan region. A mule is reared in her home for the transportation of goods. But the mule is getting older, and her family members are considering getting a new one. In this situation, she asked her father how a mule gives birth to a child. Which of the following is the correct answer given by her father?
2. Differentiate between the following:
(i) Dominant and Recessive Characters
| Feature | Dominant Character | Recessive Character |
|---|---|---|
| Expression | The character that expresses itself in the first filial (F1) generation. | The character that remains hidden or suppressed in the F1 generation. |
| Requirement | It is expressed even when only one copy of the gene is present (heterozygous state). | It is only expressed when two copies of the gene are present (homozygous state). |
| Representation | Represented by a capital letter (e.g., T for Tall). | Represented by a small letter (e.g., t for dwarf). |
| Example in Peas | Tall height, purple flowers, round seeds. | Dwarf height, white flowers, wrinkled seeds. |
(ii) Phenotype and Genotype
| Feature | Phenotype | Genotype |
|---|---|---|
| Definition | The observable physical and biochemical characteristics of an organism. | The genetic constitution or makeup of an organism. |
| Visibility | It is the external appearance (e.g., tall, short, black, white). | It is the internal genetic code, not directly visible. |
| Composition | Determined by the interaction of genotype and environmental factors. | Determined by the set of genes (alleles) inherited from the parents. |
| Example | A pea plant’s phenotype may be ‘tall’. | The same plant’s genotype could be ‘TT’ (pure tall) or ‘Tt’ (hybrid tall). |
| Ratio (Monohybrid) | The typical F2 generation ratio is 3:1. | The typical F2 generation ratio is 1:2:1. |
(iii) Inbreeding and Crossbreeding
| Feature | Inbreeding | Crossbreeding |
|---|---|---|
| Definition | Breeding between closely related individuals within the same breed. | Breeding between individuals of different breeds or species. |
| Purpose | To maintain and establish desirable traits, creating a ‘purebred’ line. | To introduce new, desirable traits and create hybrids (hybrid vigor). |
| Genetic Variation | Decreases genetic variation, leading to homozygosity. | Increases genetic variation by combining genes from different lines. |
| Risks | Increases the risk of genetic disorders and reduces fertility (inbreeding depression). | Can result in sterile offspring if species are too distantly related (e.g., mules). |
| Example | Mating between two Siamese cats to produce purebred kittens. | Mating a male lion and a female tiger to produce a Liger. |
(iv) Artificial Insemination (AI) and In-Vitro Fertilization (IVF)
| Feature | Artificial Insemination (AI) | In-Vitro Fertilization (IVF) |
|---|---|---|
| Process | Semen is collected from a male and manually deposited into the female’s reproductive tract. | Eggs are surgically removed from the female and fertilized with sperm in a laboratory dish. |
| Location of Fertilization | Fertilization occurs inside the female’s body (in-vivo). | Fertilization occurs outside the female’s body (in-vitro). |
| Main Use in Animals | Widely used in livestock breeding to improve genetic quality over a large population. | Less common in livestock; used for preserving endangered species or overcoming specific fertility issues. |
| Main Use in Humans | Used to treat certain types of male infertility or for single mothers/same-sex couples. | Used to treat complex infertility issues in both males and females (e.g., blocked fallopian tubes). |
| Complexity | Relatively simpler, less invasive, and less expensive procedure. | Highly complex, more invasive (requires hormone stimulation and egg retrieval), and more expensive. |
(v) Tigon and Liger
| Feature | Tigon | Liger |
|---|---|---|
| Parentage | Offspring of a male tiger and a female lion. | Offspring of a male lion and a female tiger. |
| Size | Generally smaller than both parents and smaller than a Liger. | The largest of all known cat species, often larger than both parents. |
| Appearance | Resembles a lion with faint tiger-like stripes. Often has a smaller mane. | Resembles a tiger with faint lion-like spots. Males can grow a mane. |
| Behavior | Tends to exhibit more lion-like social behaviors. | Tends to exhibit more tiger-like solitary behaviors. |
| Rarity | Less common than Ligers, as the mating is behaviorally less likely to occur. | More common in captivity compared to Tigons. |
3. Give reasons for the following:
(a) Children look like their parents, but not exactly the same.
Reason: Children inherit genes from both parents, which is why they share parental traits (heredity). However, they are not identical because of genetic recombination and crossing over during meiosis. This process shuffles the genes from both parents, creating a unique combination in the offspring. Furthermore, spontaneous mutations can introduce new traits not present in either parent.
(b) Mendel selected pea plants for his experiment.
Reason: Mendel chose pea plants for several key reasons:
- Short Life Cycle: They grow and reproduce quickly, allowing multiple generations to be studied in a short time.
- Many Contrasting Traits: They have several easily distinguishable characteristics (e.g., tall/dwarf, round/wrinkled seeds).
- Self-Pollination: Their flower structure allows for natural self-pollination, ensuring purebred lines could be maintained.
- Easy Cross-Pollination: They could be easily cross-pollinated manually to create hybrids.
- Large Number of Offspring: They produce many seeds, providing a large sample size for statistically significant results.
(c) When tall pea plants and dwarf pea plants are cross-pollinated, tall plants are produced in the first filial generation.
Reason: This occurs due to Mendel’s Law of Dominance. The gene for tallness (T) is dominant over the gene for dwarfness (t). When a pure tall plant (TT) is crossed with a pure dwarf plant (tt), all offspring in the F1 generation have the genotype (Tt). Because the dominant gene (T) is present, it masks the effect of the recessive gene (t), and all plants exhibit the tall phenotype.
(d) When self-breeding is done between hybrids, different types of offspring are produced.
Reason: This is explained by Mendel’s Law of Segregation (or Purity of Gametes). In a hybrid (e.g., Tt), the two alleles (T and t) coexist but remain separate. During gamete formation, these alleles segregate, so half the gametes receive the dominant allele (T) and the other half receive the recessive allele (t). When these gametes combine randomly during self-fertilization, they can produce three different genotypes: pure tall (TT), hybrid tall (Tt), and pure dwarf (tt), leading to different offspring.
(e) DNA testing is a reliable technique for criminal investigation.
Reason: DNA is unique to every individual (except identical twins). A person’s DNA profile is the same in every cell of their body (blood, hair, saliva, etc.). In criminal investigations, DNA found at a crime scene can be compared to the DNA of suspects. A match provides very strong evidence linking a suspect to the scene, making it a highly reliable and definitive identification tool.
(f) Genetic engineering involves the detailed study of DNA.
Reason: Genetic engineering is the direct manipulation of an organism’s genes. This requires a profound understanding of DNA, which is the molecule that contains the genetic instructions. Scientists must first identify the specific gene responsible for a desired trait, understand its function, and know its sequence within the DNA molecule. Only with this detailed knowledge can they accurately cut, insert, or modify the DNA to alter the organism’s characteristics.
(g) Offspring produced by cross-breeding may be sterile.
Reason: Cross-breeding between different species (interspecific hybridization) can result in sterile offspring, like the mule. This is because the two parent species have a different number or structure of chromosomes. The resulting hybrid offspring has an unmatched set of chromosomes, which prevents the proper pairing and separation of chromosomes during meiosis. Without successful meiosis, viable gametes (sperm or eggs) cannot be produced, leading to sterility.
(h) Special attention should be given while collecting samples for DNA testing.
Reason: DNA testing is a highly sensitive process. Samples can be easily contaminated with DNA from other sources (e.g., the person collecting the sample, other evidence). Contamination can lead to mixed DNA profiles, making it impossible to obtain a clear result or, worse, leading to an incorrect match and a false accusation. Therefore, strict sterile procedures and proper handling, labeling, and storage are critical to ensure the integrity and reliability of the evidence.
4. Answer the following questions:
(a) What is genetics?
Genetics is the branch of biology that deals with the study of genes, genetic variation, and heredity in living organisms. It explores how traits are passed down from one generation to the next and how genes function and interact to influence an organism’s development and characteristics.
(b) What is DNA testing? For what purposes is it used?
DNA testing (also known as DNA profiling or genetic fingerprinting) is a laboratory technique used to identify individuals based on their unique DNA sequence.
Purposes:
- Criminal Investigation: To link suspects to crime scenes or identify victims.
- Paternity Testing: To establish biological relationships between individuals, such as a father and child.
- Medical Diagnosis: To diagnose genetic disorders and determine susceptibility to certain diseases.
- Immigration: To verify family relationships for immigration purposes.
- Historical and Genealogical Research: To trace ancestry and study human migration patterns.
(c) Give some examples of genetic technology.
Examples of genetic technology include:
- Genetic Engineering: Modifying an organism’s DNA to introduce new traits (e.g., creating pest-resistant crops).
- DNA Testing/Profiling: Used in forensics and paternity tests.
- Gene Therapy: Replacing a faulty gene with a healthy one to treat genetic disorders.
- Cloning: Creating a genetically identical copy of an organism.
- Selective Breeding: Intentionally breeding organisms to promote desirable traits.
(d) Mention the importance of DNA in genetic technology.
DNA is the cornerstone of genetic technology because it is the fundamental molecule of heredity. Its importance lies in the fact that it contains the complete set of instructions (genes) for building and maintaining an organism. By understanding and manipulating DNA, scientists can:
- Identify and Isolate Genes: Pinpoint the specific genes responsible for certain traits or diseases.
- Modify Organisms: Alter an organism’s characteristics by adding, deleting, or changing genes.
- Diagnose Diseases: Detect genetic mutations that cause inherited disorders.
- Create New Products: Develop medicines, vaccines, and improved agricultural products.
(e) Explain the importance of genetic engineering.
Genetic engineering is important because it provides a powerful tool to make precise changes to an organism’s genetic makeup, with significant benefits in various fields:
- Agriculture: Development of genetically modified (GM) crops that are resistant to pests, diseases, and herbicides, have higher yields, and enhanced nutritional value.
- Medicine: Production of vital medicines like insulin, human growth hormone, and vaccines. It is also the basis for gene therapy to treat genetic diseases.
- Industry: Engineering microorganisms to produce biofuels, enzymes for detergents, and other industrial chemicals more efficiently.
- Research: Creating genetically modified organisms to study the function of genes and the mechanisms of diseases.
(f) What is a monohybrid cross? Show in a filial chart the result obtained by first cross-pollinating and then self-pollinating a red-flowering pea plant and a white-flowering pea plant.
A monohybrid cross is a genetic cross made between two pure individuals to study the inheritance of a single pair of contrasting characters.
Cross: Pure Red Flower (RR) x Pure White Flower (rr) (Assuming Red is dominant over white)
Parental Generation (P):
- Genotype: RR (Red) x rr (white)
- Gametes: R x r
First Filial Generation (F1):
- Genotype: All Rr
- Phenotype: All Red (Hybrid)
Self-Pollination of F1 Generation:
- Cross: Rr (Red) x Rr (Red)
- Gametes: R, r x R, r
Second Filial Generation (F2):
| R | r | |
|---|---|---|
| R | RR | Rr |
| r | Rr | rr |
- Genotypic Ratio: 1 RR : 2 Rr : 1 rr (1 Pure Red : 2 Hybrid Red : 1 Pure White)
- Phenotypic Ratio: 3 Red : 1 White
(g) Explain with an example that Mendel’s experiment can be done not only in plants but also in animals.
Mendel’s principles of inheritance are universal and apply to animals as well. For example, a monohybrid cross can be demonstrated using guinea pigs.
- Cross: A pure black guinea pig (BB) is crossed with a pure white guinea pig (bb). Black color (B) is dominant over white (b).
- F1 Generation: All offspring will have the genotype (Bb) and will be phenotypically black.
- F2 Generation: If two of the hybrid black guinea pigs (Bb) from the F1 generation are crossed, the offspring will appear in a phenotypic ratio of 3 black to 1 white, and a genotypic ratio of 1 BB : 2 Bb : 1 bb. This demonstrates the laws of dominance and segregation, just as in pea plants.
(h) Explain Mendel’s law of dominance and purity of gametes.
Law of Dominance: This law states that when two pure organisms with a pair of contrasting traits are crossed, only one of the traits, the “dominant” one, will appear in the F1 generation. The trait that does not appear is called “recessive.” The recessive trait only reappears in the F2 generation.
Law of Purity of Gametes (Law of Segregation): This law states that for any trait, the pair of alleles from each parent separates (segregates) during the formation of gametes (meiosis). As a result, each gamete contains only one allele for that trait. The alleles remain pure and are not blended or altered, allowing them to recombine during fertilization.
(i) A round-seeded pea plant and a wrinkle-seeded pea plant are cross-pollinated first, and then the offspring obtained were self-pollinated again. The result of the second filial generation is shown in the table below. Now answer the following questions:
| R | r | |
|---|---|---|
| R | RR | Rr |
| r | Rr | rr |
i. What is the ratio of plants showing dominant and recessive characters?
The dominant character is Round (RR, Rr) and the recessive character is wrinkled (rr). The ratio is 3 Round : 1 wrinkled. This is the phenotypic ratio.
ii. Write the genotypic and phenotypic ratio of this generation.
Genotypic Ratio: 1 RR : 2 Rr : 1 rr
Phenotypic Ratio: 3 Round : 1 wrinkled
iii. Among them, which plant is purely round-seeded? Why?
The plant with the genotype RR is purely round-seeded. This is because it is homozygous for the dominant allele, meaning it carries two identical genes for the round seed trait and can only pass on the allele for roundness to its offspring.
(j) When a cross is made between a black guinea pig and a white guinea pig, the offspring of the first filial generation were all black. Explain why white guinea pigs did not appear in this generation.
This is due to the Law of Dominance. The allele for black fur (B) is dominant over the allele for white fur (b). The pure black parent has the genotype (BB) and the pure white parent has (bb). All offspring in the F1 generation inherit one allele from each parent, resulting in the genotype (Bb). Since the dominant allele (B) is present, it masks the expression of the recessive allele (b), causing all the offspring to be black. The white trait is carried genetically but not expressed phenotypically.
(k) A teenage girl who has lost her mental balance became the victim of rape and gave birth to a child. How can the father of the child be detected?
The father of the child can be detected with a high degree of certainty using a DNA paternity test. A DNA sample would be collected from the child, the mother, and any potential suspects. A child inherits half of their DNA from their mother and half from their biological father. By comparing the child’s DNA profile to the mother’s, the DNA markers inherited from the father can be identified. The suspect whose DNA markers match the paternal markers in the child is identified as the biological father.
(l) The district animal development center conducted a camp to fertilize many cows at once. Which technique did that organization adopt at that time? Explain this technique in brief.
The organization adopted the technique of Artificial Insemination (AI).
Explanation: AI is a reproductive technology where semen is collected from a male with desirable traits (e.g., a high-quality bull). This semen is then processed, preserved (often by freezing), and later manually introduced into the reproductive tract of a receptive female (cow) at the optimal time for fertilization. This technique allows a single high-quality male to inseminate a large number of females over a wide geographic area, improving the overall genetic quality of the herd efficiently and cost-effectively.
(m) Is genetic engineering a boon or a bane for the present era? Give your arguments.
Genetic engineering can be viewed as both a boon and a bane.
Arguments for it being a BOON (a benefit):
- Increased Food Security: Development of crops with higher yields, resistance to pests and harsh environmental conditions, and improved nutritional content helps feed a growing global population.
- Medical Advancements: Production of life-saving medicines like insulin, vaccines, and growth hormones. Gene therapy offers potential cures for genetic diseases.
- Environmental Benefits: Genetically modified crops can reduce the need for chemical pesticides and herbicides, leading to less pollution.
Arguments for it being a BANE (a curse):
- Ethical Concerns: Manipulating the genetic code of living organisms, especially humans, raises profound ethical questions about “playing God.”
- Environmental Risks: The escape of genetically modified organisms into the wild could have unforeseen consequences for ecosystems and biodiversity.
- Health Concerns: There are public concerns about the long-term health effects of consuming genetically modified foods (GMOs).
- Socioeconomic Issues: The control of patented GM seeds by a few large corporations could create monopolies and disadvantage small farmers.
(n) How has Artificial Insemination (AI) technology helped to bring happiness to farmers? Explain.
AI technology has brought happiness and prosperity to farmers by:
- Improving Livestock Quality: It provides access to superior genetics from high-quality males at a low cost, leading to offspring that are healthier, more productive (more milk, meat), and more valuable.
- Reducing Costs and Risks: Farmers do not need to bear the expense and danger of maintaining large, aggressive breeding males on their farms.
- Controlling Diseases: AI helps prevent the spread of sexually transmitted diseases among livestock that can occur during natural mating.
- Increasing Efficiency: A single collection of semen can be used to inseminate many females, making breeding programs more efficient and successful. This leads to increased farm productivity and profitability.
(o) IVF has proven to be a boon for childless couples. Justify this statement.
In-Vitro Fertilization (IVF) has been a profound boon for couples struggling with infertility. It allows them to have biological children when other methods have failed.
Justification:
- Overcoming Fertility Barriers: IVF bypasses many common causes of infertility, such as blocked fallopian tubes, low sperm count, or ovulation disorders.
- Provides a Chance for Parenthood: For many, IVF is the only hope of conceiving a child, bringing immense emotional joy and fulfillment.
- Use of Donor Gametes: The technology allows for the use of donor eggs or sperm, enabling parenthood for couples where one or both partners cannot produce viable gametes.
- Genetic Screening: It allows for pre-implantation genetic diagnosis (PGD), where embryos can be screened for serious genetic diseases before being transferred to the uterus, increasing the chance of a healthy baby. For these reasons, IVF has transformed the lives of millions, helping them achieve their dream of having a family.
