Inheritance

5.2 Inheritance | Science Form 4
SCIENCE • Form 4 • Chapter 5: Genetics

5.2 Inheritance

Inheritance is the transmission of characteristics from parents to their children. While children inherit characteristics from both parents, they do not look completely identical to either parent. Characteristics such as pupil colour, hair type, and blood group are passed down through genes located on homologous chromosomes. Through systematic experiments on pea plants, Gregor Mendel uncovered the fundamental mechanisms of inheritance, demonstrating how dominant and recessive alleles interact to produce observable traits, and how similar genetic rules determine human traits and sex.

Learning Objectives

  • Define inheritance, characteristics, traits, genes, alleles, genotype, and phenotype based on textbook definitions.
  • Differentiate between dominant alleles and recessive alleles.
  • Identify examples of dominant and recessive traits in humans.
  • Describe Gregor Mendel's monohybrid cross experiments and construct schematic diagrams for \(F_1\) and \(F_2\) generations.
  • Explain the mechanism of sex determination in humans and show the 50% probability of having a male or female offspring using a schematic diagram.

Schematic Diagram of Sex Determination in Humans

Meiosis produces gametes with half the chromosome number, and random fertilisation gives an equal chance of a male or female child.

Schematic diagram of sex determination in humans A diagram showing a father with 44 + XY chromosomes and a mother with 44 + XX chromosomes. Meiosis produces two types of sperm, 22 + X and 22 + Y, and one type of ovum, 22 + X. Fertilisation between the gametes produces four possible offspring: two females with 44 + XX and two males with 44 + XY, giving a 50% to 50% ratio. Father 44 + XY Mother 44 + XX Meiosis Meiosis Sperm 22 + X Sperm 22 + Y Ovum 22 + X Ovum 22 + X Female child 44 + XX Female child 44 + XX Male child 44 + XY Male child 44 + XY 50% female : 50% male

Short Explanation

Definition

Inheritance is the transmission of characteristics from parents to their children.

Children inherit characteristics from both parents, but they do not look completely identical to either parent. Characteristics such as pupil colour, hair type, and blood group are passed down through genes located on homologous chromosomes.

Characteristics and Traits

A characteristic is a tangible property that is inherited and determined by genes. A trait is a variant of a specific characteristic that differentiates individuals.

Genes and Alleles

Genes are the basic units of inheritance found on chromosomes that control specific characteristics. An allele is a pair of genes located at the same locus or position on homologous chromosomes that control one trait of an organism. Alleles exist in dominant or recessive forms. For every trait, an individual inherits two copies of genes: one from the mother and one from the father.

Dominant and Recessive Alleles

A dominant allele expresses its characteristic and covers the effect of the recessive allele. It is represented by a capital letter, for example \(T\) for tall or \(B\) for the ability to roll the tongue.

A recessive allele has its characteristic covered in the presence of a dominant allele. It only shows its characteristic when the dominant allele is absent, meaning both alleles must be recessive, such as \(tt\) or \(bb\). It is represented by a small letter, for example \(t\) for dwarf or \(b\) for the inability to roll the tongue.

Examples of dominant and recessive traits in humans.
Characteristic Dominant trait Recessive trait
Ability to roll tongue Ability to roll tongue Inability to roll tongue
Hair colour Black hair Blonde hair
Earlobes Free earlobes Attached earlobes

Gregor Mendel and the Monohybrid Cross

Gregor Mendel (1822–1884), known as the "Father of Genetics", was the first to systematically discover the mechanism of inheritance using pea plants in monohybrid crosses.

A monohybrid cross involves the study of one characteristic at a time, for example plant height: tall versus dwarf.

Genotype and Phenotype

Genotype is the genetic information or gene combination in an organism, for example \(TT\), \(Tt\), or \(tt\). Phenotype is the physical characteristics displayed by an organism, for example tall or dwarf.

Mendel's Monohybrid Cross for Height

Parents: Pure-breeding tall (\(TT\)) \(\times\) Pure-breeding dwarf (\(tt\)).

Gametes: Meiosis separates alleles into gametes containing \(T\) and \(t\).

First Filial Generation (\(F_1\)): Genotypes are all \(Tt\) (heterozygous). Phenotypes are all tall pea plants.

Second Filial Generation (\(F_2\)): Crossing \(F_1 \times F_1\), meaning \(Tt \times Tt\), produces gametes \(T\) and \(t\) from each parent. Genotypes are \(TT\), \(Tt\), \(Tt\), and \(tt\), giving a ratio of 1 \(TT\) : 2 \(Tt\) : 1 \(tt\). Phenotypes are 3 tall : 1 dwarf, giving a phenotypic ratio of 3:1.

Human Example: Ability to Roll Tongue

A pure-breeding father able to roll his tongue (\(BB\)) \(\times\) a mother unable to roll her tongue (\(bb\)) produces all \(F_1\) offspring with genotype \(Bb\) and the phenotype of being able to roll their tongue.

Sex Determination in Humans

Humans have a total of 46 chromosomes, arranged as 23 pairs: 44 autosomes plus 2 sex chromosomes. Females have \(44 + XX\), while males have \(44 + XY\).

During gamete formation by meiosis, a sperm has half the parent chromosome number, 23 chromosomes: either \((22 + X)\) or \((22 + Y)\). An ovum also has 23 chromosomes and is always \((22 + X)\).

The gender of the offspring depends on the type of sperm fertilising the ovum. If a \((22 + X)\) sperm fertilises a \((22 + X)\) ovum, the child is female (\(44 + XX\)). If a \((22 + Y)\) sperm fertilises a \((22 + X)\) ovum, the child is male (\(44 + XY\)). Each pregnancy therefore has an equal chance of producing a male or female child: 50% female : 50% male, a 1:1 ratio.

Try to Answer First

Answer in your mind, then press "Check Answer".

1

What is the difference between genotype and phenotype?

Answer: Genotype is the genetic information or combination of alleles in an organism, for example \(TT\), \(Tt\), or \(tt\). Phenotype is the physical characteristic displayed by an organism, for example tall or dwarf.
2

In humans, what determines whether a newborn baby is male or female?

Answer: The type of sperm that fertilises the ovum determines the gender. If an ovum \((22 + X)\) is fertilised by a sperm carrying an X chromosome \((22 + X)\), the child is female (\(44 + XX\)). If it is fertilised by a sperm carrying a Y chromosome \((22 + Y)\), the child is male (\(44 + XY\)).
3

If a homozygous tall pea plant (\(TT\)) is crossed with a homozygous dwarf pea plant (\(tt\)), what are the phenotype and genotype of the \(F_1\) offspring?

Answer: The genotype of all \(F_1\) offspring is \(Tt\), and the phenotype of all \(F_1\) offspring is tall.

Common Mistakes

  • !Confusing characteristic with trait. A characteristic is the broad property, such as eye colour, while a trait is the specific variant, such as blue eyes.
  • !Misattributing gender determination to the mother. All ova carry only an X chromosome, so it is the father's sperm, carrying X or Y, that determines the child's sex.
  • !Writing different letters for the same gene, for example \(T\) for tall and \(d\) for dwarf. The correct notation uses the same letter in different cases: \(T\) and \(t\).
  • !Confusing \(F_1\) and \(F_2\) ratios. The 3:1 ratio appears only in the \(F_2\) generation when crossing two heterozygous (\(Tt \times Tt\)) individuals. The \(F_1\) generation produces 100% dominant phenotypes.

Concept Misunderstandings

Misconception

Recessive alleles are completely destroyed or altered when paired with a dominant allele.

Correct Concept

Recessive alleles remain intact and unchanged. Their physical expression is merely masked by the dominant allele, and they can reappear in subsequent generations when two recessive alleles pair together, as seen in the \(F_2\) dwarf phenotype, \(tt\).

Misconception

If a family already has three sons, their fourth child is more likely to be a daughter.

Correct Concept

Each pregnancy is an independent event. The probability of having a boy or a girl is always 50% at every single fertilisation.

Summary

  • Inheritance is the transmission of characteristics from parents to children via genes and alleles on homologous chromosomes.
  • Dominant alleles mask recessive alleles; recessive traits only appear when both alleles are recessive.
  • Gregor Mendel established the laws of inheritance through monohybrid crosses using pure-breeding pea plants, demonstrating predictable genotypic and phenotypic ratios across \(F_1\) and \(F_2\) generations.
  • Normal human body cells have 46 chromosomes: 44 autosomes and 2 sex chromosomes, \(XX\) in females and \(XY\) in males.
  • The father's sperm determines the sex of the child, giving a 50% chance for a male and a 50% chance for a female in each pregnancy.

Short Activity

A. Objective Quiz

1 Which of the following human traits is a recessive trait according to the textbook?

2 What is the chromosomal content of a normal human ovum produced after meiosis?

B. Fill in the Blanks

3 The physical characteristics shown in an organism are known as the .

 

4 In human sex determination, the percentage chance of getting a female offspring in each pregnancy is %.

 

C. Drag and Drop: Match Each Genetic Term to Its Description

Drag each term to its correct textbook description. On a phone, tap an answer first, then tap a matching box. Tap the Answer Choices area to return a selected item.

Term
Allele
Genotype
Dominant allele
Monohybrid cross
Description
1 A pair of genes at the same locus on homologous chromosomes that controls one trait.
2 The genetic information present in an organism.
3 An allele that shows its characteristic and masks the effect of an alternative allele.
4 An experiment or breeding cross involving research on only one characteristic at a time.

C. Match Each Genetic Term to Its Description

Write the correct term next to each description.

Description Term
1. A pair of genes at the same locus on homologous chromosomes that controls one trait.  
2. The genetic information present in an organism.  
3. An allele that shows its characteristic and masks the effect of an alternative allele.  
4. An experiment or breeding cross involving research on only one characteristic at a time.  

Answer choices: Allele • Genotype • Dominant allele • Monohybrid cross

Keywords

Inheritance Characteristic Trait Gene Allele Dominant allele Recessive allele Genotype Phenotype Monohybrid cross Autosome Sex chromosome

Inheritance

5.2 Inheritance | Science Form 4
SCIENCE • Form 4 • Chapter 5: Genetics

5.2 Inheritance

Inheritance is the transmission of characteristics from parents to their children. While children inherit characteristics from both parents, they do not look completely identical to either parent. Characteristics such as pupil colour, hair type, and blood group are passed down through genes located on homologous chromosomes. Through systematic experiments on pea plants, Gregor Mendel uncovered the fundamental mechanisms of inheritance, demonstrating how dominant and recessive alleles interact to produce observable traits, and how similar genetic rules determine human traits and sex.

Learning Objectives

  • Define inheritance, characteristics, traits, genes, alleles, genotype, and phenotype based on textbook definitions.
  • Differentiate between dominant alleles and recessive alleles.
  • Identify examples of dominant and recessive traits in humans.
  • Describe Gregor Mendel's monohybrid cross experiments and construct schematic diagrams for \(F_1\) and \(F_2\) generations.
  • Explain the mechanism of sex determination in humans and show the 50% probability of having a male or female offspring using a schematic diagram.

Schematic Diagram of Sex Determination in Humans

Meiosis produces gametes with half the chromosome number, and random fertilisation gives an equal chance of a male or female child.

Schematic diagram of sex determination in humans A diagram showing a father with 44 + XY chromosomes and a mother with 44 + XX chromosomes. Meiosis produces two types of sperm, 22 + X and 22 + Y, and one type of ovum, 22 + X. Fertilisation between the gametes produces four possible offspring: two females with 44 + XX and two males with 44 + XY, giving a 50% to 50% ratio. Father 44 + XY Mother 44 + XX Meiosis Meiosis Sperm 22 + X Sperm 22 + Y Ovum 22 + X Ovum 22 + X Female child 44 + XX Female child 44 + XX Male child 44 + XY Male child 44 + XY 50% female : 50% male

Short Explanation

Definition

Inheritance is the transmission of characteristics from parents to their children.

Children inherit characteristics from both parents, but they do not look completely identical to either parent. Characteristics such as pupil colour, hair type, and blood group are passed down through genes located on homologous chromosomes.

Characteristics and Traits

A characteristic is a tangible property that is inherited and determined by genes. A trait is a variant of a specific characteristic that differentiates individuals.

Genes and Alleles

Genes are the basic units of inheritance found on chromosomes that control specific characteristics. An allele is a pair of genes located at the same locus or position on homologous chromosomes that control one trait of an organism. Alleles exist in dominant or recessive forms. For every trait, an individual inherits two copies of genes: one from the mother and one from the father.

Dominant and Recessive Alleles

A dominant allele expresses its characteristic and covers the effect of the recessive allele. It is represented by a capital letter, for example \(T\) for tall or \(B\) for the ability to roll the tongue.

A recessive allele has its characteristic covered in the presence of a dominant allele. It only shows its characteristic when the dominant allele is absent, meaning both alleles must be recessive, such as \(tt\) or \(bb\). It is represented by a small letter, for example \(t\) for dwarf or \(b\) for the inability to roll the tongue.

Examples of dominant and recessive traits in humans.
Characteristic Dominant trait Recessive trait
Ability to roll tongue Ability to roll tongue Inability to roll tongue
Hair colour Black hair Blonde hair
Earlobes Free earlobes Attached earlobes

Gregor Mendel and the Monohybrid Cross

Gregor Mendel (1822–1884), known as the "Father of Genetics", was the first to systematically discover the mechanism of inheritance using pea plants in monohybrid crosses.

A monohybrid cross involves the study of one characteristic at a time, for example plant height: tall versus dwarf.

Genotype and Phenotype

Genotype is the genetic information or gene combination in an organism, for example \(TT\), \(Tt\), or \(tt\). Phenotype is the physical characteristics displayed by an organism, for example tall or dwarf.

Mendel's Monohybrid Cross for Height

Parents: Pure-breeding tall (\(TT\)) \(\times\) Pure-breeding dwarf (\(tt\)).

Gametes: Meiosis separates alleles into gametes containing \(T\) and \(t\).

First Filial Generation (\(F_1\)): Genotypes are all \(Tt\) (heterozygous). Phenotypes are all tall pea plants.

Second Filial Generation (\(F_2\)): Crossing \(F_1 \times F_1\), meaning \(Tt \times Tt\), produces gametes \(T\) and \(t\) from each parent. Genotypes are \(TT\), \(Tt\), \(Tt\), and \(tt\), giving a ratio of 1 \(TT\) : 2 \(Tt\) : 1 \(tt\). Phenotypes are 3 tall : 1 dwarf, giving a phenotypic ratio of 3:1.

Human Example: Ability to Roll Tongue

A pure-breeding father able to roll his tongue (\(BB\)) \(\times\) a mother unable to roll her tongue (\(bb\)) produces all \(F_1\) offspring with genotype \(Bb\) and the phenotype of being able to roll their tongue.

Sex Determination in Humans

Humans have a total of 46 chromosomes, arranged as 23 pairs: 44 autosomes plus 2 sex chromosomes. Females have \(44 + XX\), while males have \(44 + XY\).

During gamete formation by meiosis, a sperm has half the parent chromosome number, 23 chromosomes: either \((22 + X)\) or \((22 + Y)\). An ovum also has 23 chromosomes and is always \((22 + X)\).

The gender of the offspring depends on the type of sperm fertilising the ovum. If a \((22 + X)\) sperm fertilises a \((22 + X)\) ovum, the child is female (\(44 + XX\)). If a \((22 + Y)\) sperm fertilises a \((22 + X)\) ovum, the child is male (\(44 + XY\)). Each pregnancy therefore has an equal chance of producing a male or female child: 50% female : 50% male, a 1:1 ratio.

Try to Answer First

Answer in your mind, then press "Check Answer".

1

What is the difference between genotype and phenotype?

Answer: Genotype is the genetic information or combination of alleles in an organism, for example \(TT\), \(Tt\), or \(tt\). Phenotype is the physical characteristic displayed by an organism, for example tall or dwarf.
2

In humans, what determines whether a newborn baby is male or female?

Answer: The type of sperm that fertilises the ovum determines the gender. If an ovum \((22 + X)\) is fertilised by a sperm carrying an X chromosome \((22 + X)\), the child is female (\(44 + XX\)). If it is fertilised by a sperm carrying a Y chromosome \((22 + Y)\), the child is male (\(44 + XY\)).
3

If a homozygous tall pea plant (\(TT\)) is crossed with a homozygous dwarf pea plant (\(tt\)), what are the phenotype and genotype of the \(F_1\) offspring?

Answer: The genotype of all \(F_1\) offspring is \(Tt\), and the phenotype of all \(F_1\) offspring is tall.

Common Mistakes

  • !Confusing characteristic with trait. A characteristic is the broad property, such as eye colour, while a trait is the specific variant, such as blue eyes.
  • !Misattributing gender determination to the mother. All ova carry only an X chromosome, so it is the father's sperm, carrying X or Y, that determines the child's sex.
  • !Writing different letters for the same gene, for example \(T\) for tall and \(d\) for dwarf. The correct notation uses the same letter in different cases: \(T\) and \(t\).
  • !Confusing \(F_1\) and \(F_2\) ratios. The 3:1 ratio appears only in the \(F_2\) generation when crossing two heterozygous (\(Tt \times Tt\)) individuals. The \(F_1\) generation produces 100% dominant phenotypes.

Concept Misunderstandings

Misconception

Recessive alleles are completely destroyed or altered when paired with a dominant allele.

Correct Concept

Recessive alleles remain intact and unchanged. Their physical expression is merely masked by the dominant allele, and they can reappear in subsequent generations when two recessive alleles pair together, as seen in the \(F_2\) dwarf phenotype, \(tt\).

Misconception

If a family already has three sons, their fourth child is more likely to be a daughter.

Correct Concept

Each pregnancy is an independent event. The probability of having a boy or a girl is always 50% at every single fertilisation.

Summary

  • Inheritance is the transmission of characteristics from parents to children via genes and alleles on homologous chromosomes.
  • Dominant alleles mask recessive alleles; recessive traits only appear when both alleles are recessive.
  • Gregor Mendel established the laws of inheritance through monohybrid crosses using pure-breeding pea plants, demonstrating predictable genotypic and phenotypic ratios across \(F_1\) and \(F_2\) generations.
  • Normal human body cells have 46 chromosomes: 44 autosomes and 2 sex chromosomes, \(XX\) in females and \(XY\) in males.
  • The father's sperm determines the sex of the child, giving a 50% chance for a male and a 50% chance for a female in each pregnancy.

Short Activity

A. Objective Quiz

1 Which of the following human traits is a recessive trait according to the textbook?

2 What is the chromosomal content of a normal human ovum produced after meiosis?

B. Fill in the Blanks

3 The physical characteristics shown in an organism are known as the .

 

4 In human sex determination, the percentage chance of getting a female offspring in each pregnancy is %.

 

C. Drag and Drop: Match Each Genetic Term to Its Description

Drag each term to its correct textbook description. On a phone, tap an answer first, then tap a matching box. Tap the Answer Choices area to return a selected item.

Term
Allele
Genotype
Dominant allele
Monohybrid cross
Description
1 A pair of genes at the same locus on homologous chromosomes that controls one trait.
2 The genetic information present in an organism.
3 An allele that shows its characteristic and masks the effect of an alternative allele.
4 An experiment or breeding cross involving research on only one characteristic at a time.

C. Match Each Genetic Term to Its Description

Write the correct term next to each description.

Description Term
1. A pair of genes at the same locus on homologous chromosomes that controls one trait.  
2. The genetic information present in an organism.  
3. An allele that shows its characteristic and masks the effect of an alternative allele.  
4. An experiment or breeding cross involving research on only one characteristic at a time.  

Answer choices: Allele • Genotype • Dominant allele • Monohybrid cross

Keywords

Inheritance Characteristic Trait Gene Allele Dominant allele Recessive allele Genotype Phenotype Monohybrid cross Autosome Sex chromosome