Heredity — Class 10 Science

Revision notes for heredity.

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📌 Key Points

  • Mendel's Law of Segregation: Alleles separate during meiosis, each gamete gets one allele
  • Mendel's Law of Independent Assortment: Different traits segregate independently during meiosis
  • Dominant allele expressed in heterozygotes (Aa shows dominant phenotype), recessive masked
  • Monohybrid cross Aa × Aa: 1 AA : 2 Aa : 1 aa (genotype), 3 dominant : 1 recessive (phenotype)
  • Dihybrid cross AaBb × AaBb: 9:3:3:1 phenotypic ratio demonstrating both laws
  • DNA double helix with sugar-phosphate backbone and nitrogenous bases A, T, G, C
  • Base pairing: A-T and G-C (complementary). Ensures accurate replication and inheritance
  • Semi-conservative replication: Each new DNA has one old and one new strand
  • Gene: Stretch of DNA coding for protein/trait. Allele: Variant form of gene
  • Mutation: Change in DNA sequence (point, insertion, deletion, inversion). Creates variation
  • Autosomal traits: Affect males and females equally. Autosomal dominant/recessive
  • Sex-linked (X-linked): Gene on X chromosome. Males affected with one recessive allele, females need two
  • Carrier: Heterozygous individual (Aa or AaX for X-linked) showing dominant phenotype but carrying recessive
  • Pedigree analysis: Traces inheritance through families. Squares=male, circles=female, filled=affected
  • Genetic variation from mutations and sexual reproduction enables evolution and adaptation
  • Genotype: Genetic makeup (AA, Aa, aa). Phenotype: Observable trait
  • Homozygous: Same alleles (AA or aa). Heterozygous: Different alleles (Aa)
  • 3:1 ratio in F2 generation monohybrid cross shows Mendelian inheritance
  • X-linked recessive traits (colorblindness, hemophilia) rare in females, common in males
  • DNA → mRNA → Protein (genetic code) determines traits. Mutations alter protein production

📘 Important Definitions

Gene
Stretch of DNA on chromosome coding for specific protein or trait. Unit of heredity.
Allele
Variant form of same gene. Dominant allele expressed, recessive hidden in heterozygotes.
Genotype
Genetic composition of organism (AA, Aa, aa). Genetic makeup from parents.
Phenotype
Observable trait determined by genotype and environment. What we see.
Dominant
Allele expressed in heterozygotes. Masks recessive in Aa producing dominant phenotype.
Recessive
Allele only expressed in homozygous recessive (aa). Masked by dominant in Aa.
Homozygous
Same alleles (AA or aa). Produces only one type of gamete.
Heterozygous
Different alleles (Aa). Produces two types of gametes. Shows dominant phenotype.
Mutation
Change in DNA sequence. Point (base change), insertion (add bases), deletion (remove bases).
Genetic Variation
Differences in DNA between individuals. From mutations and sexual reproduction.

⚠️ Common Mistakes

✗ Wrong: Dominant allele is stronger or more important.

✓ Correct: Dominance just means expressed phenotypically. Both alleles equally valid. Dominance is expression pattern, not quality.

✗ Wrong: Recessive traits skip generations so next generation won't have it.

✓ Correct: Recessive traits skip visible expression but carriers pass it. Can reappear when two carriers mate.

✗ Wrong: All mutations are harmful.

✓ Correct: Mutations can be beneficial, neutral, or harmful. Beneficial mutations increase survival (natural selection).

✗ Wrong: Sex-linked traits equally common in males and females.

✓ Correct: X-linked recessive rare in females (need 2 copies) but common in males (1 copy). 20x more common in males.

✗ Wrong: Punnett square shows actual offspring, not probability.

✓ Correct: Punnett square shows probability ratios. Each cross independent - actual results may vary.

✗ Wrong: DNA replication produces two identical strands from template.

✓ Correct: Semi-conservative: Each new DNA has one old strand (template) and one new strand. Both accurate copies.

📝 Exam Focus

These questions are frequently asked in CBSE exams:

Draw Punnett square for monohybrid cross and explain 3:1 ratio.
3m
Explain Mendel's Law of Segregation and Independent Assortment.
5m
Compare autosomal and sex-linked inheritance with examples.
5m
Describe DNA structure and semi-conservative replication.
5m
Explain genotype vs phenotype with examples.
3m
Analyze pedigree to determine inheritance pattern and predict offspring.
5m
Explain mutation types and genetic variation importance.
3m
Apply base pairing rules to write complementary DNA strand.
3m

🎯 Last-Minute Recall

Close your eyes and try to recall: Key definitions, formulas, and 3 common mistakes. If you can recall 80% without looking, you're exam-ready!