class 10 Biology: Heredity : notes

Heredity

Class 10 CBSE Science • Chapter 8 • Easy, colourful notes for kids

1. What is Heredity?

Heredity: the passing of genetic information and characters (traits) from one generation to the next.
Variation: the differences in characters among the individuals of a species.
Genetics: the branch of biology which deals with the study of heredity and variation.

Eye colour

brown, blue, green

Flower colour

pink, yellow, white, red

Earlobes

attached or free

Thumb

straight or bent

Family looks

child looks like parents

All these differences between individuals are examples of variation.

2. Inherited Traits vs Acquired Traits

Inherited traitsAcquired traits
These traits can be inherited as well as transmitted to the next generation.These traits are neither inherited nor transmitted to the next generation.
Inherited from parents during reproduction.Acquired after birth.
Examples: skin colour, eye colour, nose shape, blood group, etc.Examples: acquiring weight, piercing of ear or nose, acquiring knowledge, etc.
Tip: Born with it → inherited. Got it later in life → acquired (and it is not passed to children).

3. Some Important Terms

These are the terms we will learn in this chapter. Tap a name to jump to its section.

4. DNA, Chromosomes and Chromosome Number

DNA (Deoxyribo Nucleic Acid)

  • It is a double-stranded, thread-like structure present in the nucleus.
  • It carries all the information about the structure and function of an organism.
  • It is inherited from one generation to another.
DNA double helix
DNA is a double helix (double-stranded thread)

Chromatin and Chromosome

DNA is packed with proteins. In a normal (non-dividing) cell it looks like a tangled chromatin thread. When the cell divides, the chromatin condenses into short, thick chromosomes.

DNA → Chromatin (tangled thread) —(cell division)→ Chromosome (condensed, rod-like)

Haploid and Diploid

Haploid (n)

  • Single copy of each chromosome.
  • Chromosome number is denoted as ‘n’. Here n = 4.

Diploid (2n)

  • Two copies of each chromosome.
  • Chromosome number is denoted as 2n. Here 2n = 2 × 4 = 8.

Chromosome number in human body cells and gametes

  • All cells of the human body are diploid, except gametes.
  • Gametes (sperm cell and egg cell) are haploid cells.
Total chromosomes in a human cell = 46 (23 pairs)
CellTypeChromosomes
Female body cellDiploid46
Male body cellDiploid46
Egg cell / ovum (made by meiosis)Haploid23
Sperm cell (made by meiosis)Haploid23
Zygote (after fertilisation)Diploid46 (23 pairs)
Egg (23) + Sperm (23) —(fertilisation)→ Zygote (46 = 23 pairs)
  • The chromosome that comes from the mother is the maternal chromosome.
  • The chromosome that comes from the father is the paternal chromosome.
  • A maternal and a paternal chromosome of the same kind form a pair called homologous chromosomes.

5. Genes and Alleles

Genes

Gene: a segment or part of DNA that carries the information for a particular character. Gene → Information → Protein.

One DNA thread has many genes, for example a gene for blood group, a gene for eye colour and a gene for hair shape.

Alleles

Allele: an alternative variant, version or form of a gene. Two or more possible forms of a gene are located at a specific location (place) on a specific chromosome.
Gene → Dominant allele or Recessive allele
Gene forAllele 1Allele 2
Plant heightT = Tall (dominant)t = Dwarf (recessive)
Colour of flowerVioletWhite
Seed shapeR = Round seedr = Wrinkled seed

Dominant Allele vs Recessive Allele

Dominant alleleRecessive allele
The stronger one of the two alleles.The weaker one of the two alleles.
Denoted by a capital letter (T).Denoted by a small letter (t).
Expresses itself in both: homozygous condition (TT) and heterozygous condition (Tt).Expresses itself only in the homozygous condition (tt).

6. Phenotype vs Genotype, Homozygous vs Heterozygous

Phenotype vs Genotype

PhenotypeGenotype
The appearance of an organism, or its observable physical trait.
Example: tall or dwarf plant, round or wrinkled seed.
The combination of genes in an organism.
Example: TT, Tt, tt.
Example (eye colour): Dad has brown eyes (dominant, B). Mom has blue eyes (recessive, b). The child has genotype Bb, so the child shows brown eyes (phenotype), and the blue colour stays hidden.
Dad BB (brown) + Mom bb (blue) → Child Bb (brown displayed, blue hidden)

Homozygous and Heterozygous conditions

Homozygous dominant
(pure condition)

RR

Round seed (RR)
Tall (TT)

Heterozygous
(hybrid condition)

Rr

Round seed (Rr)
Tall (Tt)
one dominant + one recessive allele

Homozygous recessive
(pure condition)

rr

Wrinkled seed (rr)
Dwarf (tt)

Tip: Homo = same, so both alleles are the same (TT or tt). Hetero = different, so the alleles are different (Tt).

7. Mendel and His Contributions

Gregor Mendel
Gregor Johann Mendel (1822–1884)
  • ✔️ Gregor Johann Mendel (1822–1884).
  • ✔️ Known as the “Father of Genetics”.
  • ✔️ Performed his hybridisation experiments on pea plants from 1856 to 1863 and published the result in 1866.
  • ✔️ His work explained how traits are inherited from one generation to the next and proposed the laws of inheritance.

Seven pairs of contrasting traits in the pea plant (Pisum sativum, the garden pea)

TraitShape of seedsColour of seedsColour of podsShape of podsPlant heightPosition of flowersFlower colour
Dominant traitRoundYellowGreenFullTallAt leaf junctionPurple
Recessive traitWrinkledGreenYellowFlat, constrictedShortAt tips of branchesWhite

Hybridisation experiments

Mendel took pollen grains from the anther of one pea plant (parent P1) and placed them on the stigma of another plant (parent P2). This is cross-pollination.

After fertilisation:
1) Zygote → Embryo
2) Ovule → Seed
3) Ovary → Fruit

Mendel’s Laws of Inheritance

Based on a Monohybrid Cross:
(i) Law of Dominance: When an inherited pair of two alleles is heterozygous, the allele that is expressed is called dominant, while the other is called recessive.
(ii) Law of Segregation: During gamete formation, the copies of genes or alleles are divided (segregated) such that each gamete receives only one allele.
Based on a Dihybrid Cross:
(iii) Law of Independent Assortment: Alleles of two or more different genes get assorted into gametes independently of one another.

Breeding pea plants with violet flowers and white flowers

Parental generation (P): Violet flower plant × White flower plant
First generation (F1): 100% plants have purple (violet) flowers

8. Monohybrid Cross (one character)

Monohybrid cross: a cross in which only one character is studied at a time.

In his first monohybrid cross, Mendel crossed a pure-breed tall plant and a pure-breed dwarf plant.

  • Tall: TT = Pure tall, Tt = Hybrid tall.
  • Dwarf: tt = Dwarf.

Steps of the cross (tall × dwarf)

Parent: Pure Tall TT × Pure Dwarf tt
↓
Gametes: T and T  |  t and t
↓ Fertilisation
F1 generation: Tt
Genotype = Heterozygous
Phenotype = Hybrid Tall plant
↓ Selfing (F1 × F1: Tt × Tt)
Gametes: T, t  |  T, t
↓
F2 generation: TT, Tt, Tt, tt

F2 generation (Punnett square)

♀ ♂Tt
TTT
Tall
Tt
Tall
tTt
Tall
tt
Dwarf

Phenotypic ratio in F2

Tall : Dwarf = 3 : 1
75% Tall, 25% Dwarf

Genotypic ratio in F2

TT : Tt : tt = 1 : 2 : 1
Homozygous dominant TT 25%
Heterozygous Tt 50%
Homozygous recessive tt 25%

Another example: flower colour (Blue × White)

Parent: Blue flower BB × White flower bb
↓
Gametes: B and B  |  b and b
↓
F1: Bb = Heterozygous blue flower
↓ Selfing (F1 × F1: Bb × Bb)
Gametes: B, b  |  B, b
♀ ♂Bb
BBB
blue
Bb
blue
bBb
blue
bb
white
  • Phenotypic ratio: Blue 75% : White 25% (3 : 1).
  • Genotypic ratio: BB : Bb : bb = 1 : 2 : 1.

2️⃣ 9. Dihybrid Cross (two characters)

Dihybrid cross: a cross in which the inheritance of two characters is studied at a time.

Mendel studied the inheritance of two characters:

Seed shape

Round (R) and Wrinkled (r)

Seed colour

Yellow (Y) and Green (y)

Steps of the cross (round green × wrinkled yellow)

Parent: Round, green RRyy × Wrinkled, yellow rrYY
↓
Gametes: Ry  |  rY
↓ Fertilisation
F1 generation: RrYy = Round, yellow seeds
↓ Selfing (F1 × F1: RrYy × RrYy)
Gametes: RY, Ry, rY, ry  |  RY, Ry, rY, ry

F2 generation (Punnett square, 16 boxes)

♀ ♂RYRyrYry
RYRRYYRRYyRrYYRrYy
RyRRYyRRyyRrYyRryy
rYRrYYRrYyrrYYrrYy
ryRrYyRryyrrYyrryy

Round, Yellow Round, Green Wrinkled, Yellow Wrinkled, Green

Phenotypic ratio in F2

9 : 3 : 3 : 1
Round yellow : Round green : Wrinkled yellow : Wrinkled green

Genotypic ratio in F2

1 : 2 : 2 : 4 : 1 : 2 : 1 : 2 : 1
RRYY : RRYy : RrYY : RrYy : RRyy : Rryy : rrYY : rrYy : rryy
Mendel’s actual result (556 seeds): 315 round yellow, 108 round green, 101 wrinkled yellow and 32 wrinkled green, which is close to 9 : 3 : 3 : 1. Notice that new combinations (round green and wrinkled yellow) appeared in F2, which shows that the two characters are inherited independently.

⚧ 10. Sex Determination

Sex determination: the process by which the sex of a newborn individual is determined.

Factors affecting sex determination

🧬 Genetically

In humans, the chromosomes (genes) inherited from the parents decide the sex of the offspring.

🌡️ Non-genetically (environmental cues)

In turtles, alligators and crocodiles, the temperature at which the fertilised eggs are kept decides the sex. In snails, individuals can change sex.
SpeciesTemperature effectSex produced
TurtlesLow (26–28°C)Male 🐢
TurtlesHigh (31–33°C)Female 🐢
CrocodilesLow or highFemale 🐊
CrocodilesMediumMale 🐊

Human chromosomes: Autosomes and Allosomes

Human male karyotype
Human karyotype (all 23 pairs of chromosomes arranged in order)
AutosomesAllosomes (sex chromosomes)
Chromosomes that are not involved in determining sex.Chromosomes involved in determining the sex of an individual.
Similar in males and females.Male is XY and female is XX (not similar in males).
In humans there are usually a total of 44 or 22 pairs.In humans there is usually 1 pair (2 chromosomes).
Sex chromosomes: Male = XY, Female = XX.

Cross between sex chromosomes

Parent: Male XY × Female XX
Gametes: X, Y  |  X, X
♂ sperm
♀ egg
XY
XXX
(Girl)
XY
(Boy)
XXX
(Girl)
XY
(Boy)

Boy : Girl = 1 : 1 and XY : XX = 1 : 1

Sex determination in human beings

FATHER XYMOTHER XXXYXXGametesXXFEMALEXXFEMALEXYMALEXYMALE50% Female child50% Male child
Zygote formed after fusion of gametes. Solid lines = father’s gamete, dashed lines = mother’s gamete.
  • If a sperm with X chromosome fertilises the egg, the zygote will have XX in the 23rd pair. A zygote with XX will develop into a girl child.
  • If a sperm with Y chromosome fertilises the egg, the zygote will have XY in the 23rd pair. A zygote with XY will develop into a male (boy) child.
  • There is a 50% probability of a female child and a 50% probability of a male child.
Remember: The mother always gives an X. The father’s sperm (X or Y) decides whether the baby is a girl or a boy.

11. Quick Revision

Heredity

Passing of traits from one generation to the next

Variation

Differences among individuals of a species

Human chromosomes

46 (23 pairs); gametes 23

Dominant

Capital letter (T), shows in TT and Tt

Recessive

Small letter (t), shows only in tt

Monohybrid F2

Phenotype 3 : 1, Genotype 1 : 2 : 1

Dihybrid F2

Phenotype 9 : 3 : 3 : 1

Mendel

Father of Genetics, pea plant, 1856–1863, published 1866

Sex chromosomes

Male XY, Female XX

Boy : Girl

1 : 1 (50% each)

All the best for your exams!