🧬 Chapter 4: Principles of Inheritance and Variation – Class 12 Biology --4Marks Questions with Answers | NCERT + NEET Focus

Rashmi Mishra
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🌸 Chapter 4

Principles of Inheritance and Variation 

(4 Marks)

1. Explain Mendel’s Law of Segregation with an example.

Answer:

  • Law: During gamete formation, alleles of a gene separate so that each gamete receives only one allele.
  • Example: In a monohybrid cross between tall (TT) and dwarf (tt) pea plants, F1 are all tall (Tt). In F2, segregation produces genotypes TT, Tt, and tt in a 1:2:1 ratio, giving 3 tall : 1 dwarf plants.
  • Conclusion: Alleles do not blend but separate during gamete formation.

2. State Mendel’s Law of Independent Assortment. Explain with a dihybrid cross.

Answer:

  • Law: Genes for different traits assort independently during gamete formation.
  • Example: Crossing round yellow (RRYY) with wrinkled green (rryy) gives F1 = RrYy (round yellow).
  • F2 phenotypic ratio = 9 round yellow : 3 round green : 3 wrinkled yellow : 1 wrinkled green.
  • Conclusion: Inheritance of one character does not affect another.

3. Explain the difference between incomplete dominance and co-dominance with examples.

Answer:

Basis

Incomplete Dominance

Co-dominance

Expression

Intermediate trait appears

Both alleles express equally

Example

Snapdragon (RR × rr → Rr = pink)

ABO blood group (IAIB = AB)

Result

Blending appearance

Equal expression of both traits


4. What is test cross? Explain its importance.

Answer:

  • Definition: Crossing an individual with a dominant phenotype with a homozygous recessive individual.
  • Example: T? × tt
  • Purpose: To determine whether the dominant phenotype is homozygous (TT) or heterozygous (Tt).
  • Importance: Helps confirm Mendel’s Law of Segregation.

5. Describe the chromosomal theory of inheritance.

Answer:

  • Proposed by Sutton and Boveri (1902).
  • Key points:
    • Genes are located on chromosomes.
    • Homologous chromosomes segregate during meiosis.
    • Independent assortment of chromosomes explains Mendel’s dihybrid ratios.
  • Thus, chromosomes are the carriers of genes and hence of heredity.

6. What is linkage? Explain Morgan’s experiment on linkage in Drosophila.

Answer:

  • Definition: Tendency of genes on the same chromosome to be inherited together.
  • Experiment: Morgan crossed yellow-bodied white-eyed (X-linked traits) with normal flies.
  • Observed that genes did not assort independently — they were linked.
  • Conclusion: Closer the genes on a chromosome, stronger the linkage.

7. Define recombination. How did Morgan and Sturtevant explain it?

Answer:

  • Definition: Formation of new combinations of genes due to crossing over.
  • Morgan found recombination frequency depends on distance between genes.
  • Sturtevant prepared genetic maps using recombination frequency (1% = 1 map unit).
  • Conclusion: Recombination is the basis for gene mapping.

8. What is pleiotropy? Explain with an example.

Answer:

  • Definition: When one gene influences multiple traits.
  • Example: In pea plants, the gene for starch synthesis also affects seed shape.
    • Round seeds (RR) have more starch, wrinkled (rr) have less.
  • Human example: Sickle cell anemia gene affects RBC shape and oxygen transport.

9. Differentiate between genotype and phenotype.

Answer:

Feature

Genotype

Phenotype

Meaning

Genetic constitution

Observable traits

Example

TT, Tt, tt

Tall, dwarf

Dependence

Fixed by genes

Affected by genes + environment

Mendelian ratio

1:2:1 (genotypic)

3:1 (phenotypic)


10. Explain multiple allelism with the example of human ABO blood groups.

Answer:

  • Definition: When a gene exists in more than two allelic forms.
  • Example: Gene ‘I’ has three alleles – IA, IB, i.
    • IAIA / IAi = A group
    • IBIB / IBi = B group
    • IAIB = AB group (co-dominant)
    • ii = O group
  • Each person carries only two alleles, though multiple exist in the population.

11. What are sex-linked traits? Explain with one example.

Answer:

  • Traits whose genes are located on sex chromosomes.
  • Example: Haemophilia – a recessive X-linked disorder.
    • Gene on X chromosome → males (XY) show disease, females (XX) are carriers.
  • Conclusion: Males are more frequently affected due to single X chromosome.

12. What are multiple factors or polygenic inheritance? Give an example.

Answer:

  • Definition: A trait controlled by more than one gene pair.
  • Example: Human skin color, height, intelligence.
    • In skin color, 3 gene pairs contribute additively.
    • More dominant alleles → darker color.
  • Conclusion: Shows continuous variation in population.

13. Explain the inheritance of sex in humans.

Answer:

  • Females: XX, produce only X-bearing ova.
  • Males: XY, produce both X and Y-bearing sperms.
  • If sperm with X fertilizes → girl (XX); with Y → boy (XY).
  • Conclusion: Father determines the sex of the child.

14. Explain the mechanism of sex determination in honeybee.

Answer:

  • Haplodiploid mechanism:
    • Fertilized eggs (2n) → females (queen/workers).
    • Unfertilized eggs (n) → males (drones).
  • Conclusion: Females are diploid, males haploid; sex determined by ploidy level.

15. Describe sickle cell anemia and its inheritance pattern.

Answer:

  • Cause: Mutation in β-globin gene (GAG → GTG) → Valine replaces Glutamic acid.
  • Genotypes:
    • HbA HbA – normal
    • HbA HbS – carrier (mild)
    • HbS HbS – sickle cell anemia (severe)
  • Inheritance: Autosomal recessive; both parents must carry the defective gene.

16. What is the difference between autosomes and sex chromosomes?

Answer:

Feature

Autosomes

Sex Chromosomes

Number

22 pairs

1 pair

Function

Determine somatic traits

Determine sex and related traits

In Humans

44 autosomes

XX (female), XY (male)

Example

Eye color, height

Color blindness, haemophilia


17. What is mutation? Differentiate between gene and chromosomal mutation.

Answer:

  • Mutation: Sudden heritable change in DNA sequence or chromosome structure.
    | Type | Definition | Example |
    |------|-------------|----------|
    | Gene mutation | Change in DNA base sequence | Sickle cell anemia |
    | Chromosomal mutation | Change in chromosome number/structure | Down’s syndrome |

18. Write a short note on Down’s syndrome.

Answer:

  • Cause: Trisomy of chromosome 21.
  • Symptoms: Mental retardation, broad face, short stature, furrowed tongue.
  • Karyotype: 47 chromosomes (2n + 1).
  • Type: Autosomal aneuploidy.

19. Explain Turner’s syndrome and Klinefelter’s syndrome.

Answer:

Syndrome

Karyotype

Characteristics

Turner’s

45, XO

Females, short, sterile, underdeveloped ovaries

Klinefelter’s

47, XXY

Males, tall, sterile, feminine traits


20. Define pedigree analysis. How is it useful?

Answer:

  • Definition: Diagram showing inheritance pattern across generations.
  • Uses:
    • Identify carriers of genetic diseases.
    • Predict probability of inheritance.
    • Helps in genetic counseling and disease prevention.

21. Differentiate between dominance, incomplete dominance, and co-dominance.

Answer:

Type

Expression

Example

Dominance

One allele masks another

Pea plant (Tt = tall)

Incomplete dominance

Intermediate phenotype

Snapdragon (Rr = pink)

Co-dominance

Both alleles express equally

Blood group (IAIB = AB)


22. What is gene mapping? Explain its importance.

Answer:

  • Definition: Determining the relative positions of genes on a chromosome.
  • Basis: Recombination frequency.
  • Importance:
    • Helps locate disease genes.
    • Used in genome projects and plant breeding.

23. What are the reasons for Mendel’s success in his experiments?

Answer:

  • Used pure lines and distinct contrasting traits.
  • Conducted controlled crosses.
  • Quantitative analysis of results.
  • Studied one/two traits at a time.
  • Maintained statistical accuracy.

24. Why was Mendel’s work not recognized immediately?

Answer:

  • Published in an obscure journal.
  • Concepts ahead of his time.
  • No knowledge of chromosomes or meiosis then.
  • Rediscovered in 1900 by De Vries, Correns, and Tschermak.

25. Differentiate between linkage and independent assortment.

Answer:

Feature

Linkage

Independent Assortment

Definition

Genes inherited together

Genes assort independently

Location

Same chromosome

Different chromosomes

Effect

Reduces recombination

Increases variation

Example

Drosophila body color & wing size

Pea seed color & shape

 

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