🧬 NEET 2026 – Genetics & Evolution (Full Notes)
1. Heredity & Variation
Mendelian Inheritance
Parent Genotype → Law of Segregation (Alleles separate during gamete formation) → Gamete Formation (Each gamete carries one allele) → Fertilization (Random fusion of gametes) → F1 Generation
- Genotypic Ratio: 1:2:1
- Phenotypic Ratio: 3:1
Dihybrid Cross: Two traits, e.g., Seed shape × Seed color → Independent Assortment (Genes on different chromosomes) → Gametes → 4 types (RY, Ry, rY, ry) → F1 Generation
- Phenotypic Ratio: 9:3:3:1
- Genotypic Ratio: 1:2:2:4:1:2:1:2:1
Deviations from Mendelism
- Incomplete Dominance: Heterozygote shows intermediate phenotype. Example: Snapdragon Flower (Red × White → Pink)
- Codominance: Both alleles express. Example: AB Blood Group (IAIB)
- Multiple Alleles: More than 2 alleles per gene. Example: ABO system (IA, IB, i)
- Pleiotropy: One gene affects multiple traits. Example: Phenylketonuria → Mental retardation + skin issues
- Polygenic Inheritance: Many genes control one trait → continuous variation. Example: Skin color, Height
ABO Blood Group System
| Genotype | Blood Group |
|---|---|
| IAIA / IAi | A |
| IBIB / IBi | B |
| IAIB | AB |
| ii | O |
Note: IA & IB → codominant, i → recessive
Sex Determination & Sex-linked Traits
- Humans → XX/XY
- Birds → ZZ/ZW
- Honey Bee → Haplodiploidy (Male = haploid, Female = diploid)
- X-linked Traits: Mostly in males (XY). Examples: Haemophilia, Colour blindness
Genetic Disorders
- Mendelian Disorders: Thalassemia → Autosomal Recessive
- Chromosomal Disorders:
Disorder Cause Key Feature Down Syndrome Trisomy 21 Mental retardation, short stature Turner Syndrome XO Female, sterile, short stature Klinefelter Syndrome XXY Male, tall, sterile
2. Molecular Basis of Inheritance
Discovery of DNA as Genetic Material
- Griffith (1928): Transformation experiment
- Avery, MacLeod & McCarty: DNA responsible for transformation
- Hershey-Chase (1952): DNA enters bacteriophage, protein does not
DNA Structure (Watson & Crick)
- Double helix, antiparallel strands
- Base pairing: A=T, G≡C
- DNA Packaging: DNA + Histones → Nucleosome → Chromatin → Chromosome
DNA Replication (Semi-Conservative)
- Steps:
- Origin of Replication (Ori) → replication bubble forms
- Helicase unwinds DNA, SSB stabilizes strands
- Primase synthesizes RNA primers
- DNA Pol III adds nucleotides (Leading continuous, Lagging → Okazaki fragments)
- DNA Pol I replaces RNA primers with DNA
- DNA ligase joins fragments
- Replication terminates
Transcription (DNA → RNA)
- Initiation: RNA polymerase binds promoter, unwinds DNA
- Elongation: RNA synthesized 5’→3’, base pairing: A→U, T→A, G→C, C→G
- Termination: RNA transcript released
- Post-transcriptional modifications (eukaryotes): 5’ cap, 3’ poly-A tail, splicing
Translation (mRNA → Protein)
- Initiation: Small ribosomal subunit + mRNA + tRNA(Met) → Initiation complex
- Elongation: Ribosome moves codon by codon, tRNA brings amino acids, peptide bonds formed
- Termination: Stop codon reached → Release factor → Polypeptide released
- Post-translational modification: Folding, addition of groups, cleavage if necessary
Gene Regulation – Lac Operon
- Lactose Absent → Repressor binds → Gene OFF
- Lactose Present → Repressor removed → Gene ON
DNA Fingerprinting
DNA Sample → Restriction Enzyme → Gel Electrophoresis → Band Pattern → Identification
Applications: Forensics, Paternity Testing
Human Genome Project
DNA Sequencing → Mapping Genes → Genome Database → Applications
3. Evolution
Origin of Life
- Primordial Soup Theory (Oparin)
- Chemical evolution → First prokaryotes
Evidences of Evolution
- Fossils → Geological record
- Comparative Anatomy → Homologous/Analogous structures
- Embryology → Similar embryonic stages
- Molecular Biology → DNA & Protein sequence similarity
Darwinian Natural Selection
Variation → Struggle for Existence → Survival of the Fittest → Evolution
Modern Synthetic Theory: Combines Darwin + Mendelian Genetics
Mechanism of Evolution
- Sources of Variation: Mutation, Recombination
- Types of Natural Selection:
- Stabilizing → favors mean
- Directional → favors one extreme
- Disruptive → favors both extremes
- Other Factors: Gene Flow, Genetic Drift → Population Evolution → Speciation
Adaptive Radiation & Human Evolution
Common Ancestor → Adaptive Radiation → Multiple Species
Human Evolution: Australopithecus → Homo habilis → Homo erectus → Homo sapiens
Hardy-Weinberg Principle
Allele Frequencies: p + q = 1
Genotype Frequencies: p² + 2pq + q² = 1
Conditions: No mutation, No migration, Large population, Random mating, No selection
Conclusion
These comprehensive notes cover all key concepts of Genetics and Evolution for NEET 2026, including Mendelian inheritance, molecular basis of inheritance, gene regulation, DNA fingerprinting, and evolutionary mechanisms. The stepwise flow of replication, transcription, and translation ensures easy understanding and quick revision. Students can use this as a last-minute revision guide to strengthen conceptual clarity and enhance problem-solving skills for NEET exams.

