NEET · Subject-wise preparation
Genetics and evolution for NEET: concepts, problems and traps
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Genetics and Evolution is unit 7 of the NMC's 10 Biology units, and it is the one Biology unit that mixes recall with calculation: crosses, ratios, pedigrees, a base-sequence question, and a Hardy-Weinberg sum. Learn it in four blocks: the principles of inheritance, the chromosomal basis and sex determination, the molecular basis (DNA to RNA to protein), and evolution. This page owns the depth; the overall Biology approach is in NEET Biology preparation.
What the unit covers
The NMC lists Genetics and Evolution as a single unit. The breakdown below follows the usual NCERT chapters, which is our mapping.
| Block | Core ideas | Question types |
|---|---|---|
| Principles of inheritance and variation | Mendel's laws, dominance, incomplete dominance, codominance, multiple alleles, linkage, sex determination, pedigrees, mutations, genetic disorders | Cross problems, ratio questions, pedigree reading, statements on disorders |
| Molecular basis of inheritance | DNA as genetic material, structure, replication, transcription, genetic code, translation, lac operon, genome studies | Experiment-conclusion matching, base sequences, operon logic |
| Evolution | Origin of life, evidence, natural selection, Hardy-Weinberg principle, adaptive radiation, human evolution | Recall, matching, one numerical |
For how often the unit is asked relative to others, see NEET high weightage chapters.
Mendelian ratios you must know cold
| Cross | Genotype ratio | Phenotype ratio |
|---|---|---|
| Monohybrid Aa × Aa (complete dominance) | 1 AA : 2 Aa : 1 aa | 3 : 1 |
| Test cross Aa × aa | 1 Aa : 1 aa | 1 : 1 |
| Incomplete dominance, Aa × Aa | 1 : 2 : 1 | 1 : 2 : 1 |
| Dihybrid AaBb × AaBb | 9 genotypes | 9 : 3 : 3 : 1 |
| Dihybrid test cross AaBb × aabb | 1 : 1 : 1 : 1 | 1 : 1 : 1 : 1 |
The classic trap is incomplete dominance and codominance, where the phenotype ratio is the same as the genotype ratio. In codominance, such as the I^A and I^B alleles of the ABO blood group, both alleles are fully expressed in the heterozygote, which is why I^A I^B gives blood group AB.
Worked problems
Product rule. For RrYy × RrYy, the chance of a wrinkled, green (rryy) offspring is the chance of rr times the chance of yy: 1/4 × 1/4 = 1/16. The chance of round and yellow is 3/4 × 3/4 = 9/16. Multiplying single-gene probabilities is faster than drawing a 16-box square.
Blood groups. A parent of genotype I^A i and another of genotype I^B i can have children of groups AB, A, B and O, each with probability 1/4.
X-linked inheritance. A carrier mother (X^H X^h) and a normal father (X^H Y) give four equally likely children: a normal daughter, a carrier daughter, a normal son and a haemophilic son. So half the sons are affected, and no daughter is affected.
Hardy-Weinberg. If 16% of a population shows a recessive trait, then q² = 0.16, so q = 0.4 and p = 0.6. Carriers are 2pq = 2 × 0.6 × 0.4 = 0.48, or 48%. Check: 0.36 + 0.48 + 0.16 = 1.
Reading pedigrees
- Two unaffected parents with an affected child point to a recessive trait.
- If every affected person has an affected parent, suspect a dominant trait.
- A trait that skips generations and affects mainly males suggests X-linked recessive. An affected father cannot pass an X-linked trait to a son.
- Decide dominant or recessive first, then autosomal or X-linked, and test the answer on every family in the chart.
Sex determination and linkage
- Humans: XX female, XY male, so the male is heterogametic.
- Birds: ZW female, ZZ male, so the female is heterogametic.
- Grasshopper: XX female, XO male.
- Honey bee: haplodiploid. Drones develop from unfertilised eggs and are haploid; queens and workers are diploid.
Linked genes on the same chromosome do not assort independently. The closer two genes are, the fewer the recombinants, and one percent recombination equals one map unit. Morgan's work on Drosophila is the standard example.
Genetic disorders
| Disorder | Type | Fact to remember |
|---|---|---|
| Haemophilia | X-linked recessive | Defective blood clotting; a daughter is affected only if the father is affected and the mother is at least a carrier |
| Colour blindness | X-linked recessive | Red-green defect, more common in males |
| Sickle-cell anaemia | Autosomal recessive | One base substitution, GAG to GUG in mRNA, replaces glutamic acid with valine at position 6 of the β-globin chain |
| Thalassaemia | Autosomal recessive | Reduced synthesis of α or β globin chains; a quantitative defect, unlike sickle-cell, which is structural |
| Phenylketonuria | Autosomal recessive | Deficiency of the enzyme phenylalanine hydroxylase |
| Down syndrome | Trisomy 21 | 47 chromosomes |
| Turner syndrome | 45, XO | Female, sterile |
| Klinefelter syndrome | 47, XXY | Male with feminine development, sterile |
Molecular basis: experiments and numbers
| Experiment | Conclusion |
|---|---|
| Griffith, 1928 (Streptococcus pneumoniae, smooth and rough strains) | A "transforming principle" passes from dead smooth cells to live rough cells |
| Avery, MacLeod and McCarty, 1944 | DNA is the transforming principle: DNase stopped transformation, while protease and RNase did not |
| Hershey and Chase, 1952 (³²P and ³⁵S in bacteriophage) | Radioactive DNA, not protein, entered the bacterium: DNA is the genetic material |
| Meselson and Stahl, 1958 (¹⁵N then ¹⁴N, CsCl density gradient) | DNA replication is semi-conservative |
Chargaff's rule is A = T and G = C. In B-DNA there are 10 base pairs per turn, a pitch of 3.4 nm, and 0.34 nm between adjacent base pairs.
The genetic code
The code is triplet and degenerate, and it is nearly universal. There are 64 codons: 61 code for amino acids and three (UAA, UAG, UGA) are stop codons. AUG codes for methionine and is the start codon.
Worked problem. A template strand reads 3′-TACGGA-5′. The mRNA is built antiparallel and complementary: 5′-AUGCCU-3′. Reading codons gives AUG (methionine) and CCU (proline). Always work out which strand is the template before transcribing, since the coding strand has the same sequence as the mRNA, with T replaced by U.
Operon and genome
In the lac operon, the i gene codes for a repressor. Without lactose the repressor binds the operator and blocks transcription. Lactose, the inducer, binds the repressor and the structural genes lacZ, lacY and lacA are transcribed. The Human Genome Project established that the human genome has about 3 × 10⁹ base pairs. DNA fingerprinting uses variable number tandem repeats (VNTRs).
Evolution
| Topic | What to know |
|---|---|
| Origin of life | Oparin-Haldane chemical evolution; Miller-Urey (1953) produced amino acids from methane, ammonia, hydrogen and water vapour under electric discharge |
| Evidence | Homologous organs (same origin, different function) show divergent evolution; analogous organs (different origin, same function) show convergent evolution; vestigial organs; fossils |
| Natural selection | Stabilising, directional and disruptive selection; industrial melanism in the peppered moth is the standard example |
| Adaptive radiation | Darwin's finches and Australian marsupials |
| Hardy-Weinberg | p + q = 1 and p² + 2pq + q² = 1; equilibrium is disturbed by gene flow, genetic drift, mutation, genetic recombination and natural selection |
| Human evolution | Brain capacity: Homo habilis about 650 to 800 cc, Homo erectus about 900 cc, Neanderthals about 1,400 cc |
Mistakes that cost marks
- Giving a genotype ratio when the question asks for the phenotype ratio, or the reverse.
- Writing gametes wrongly: from AaBb they are AB, Ab, aB and ab, not Aa and Bb.
- Mixing up the template and coding strands, or forgetting that mRNA is antiparallel to the template.
- Applying Hardy-Weinberg without its assumptions: a large population, random mating, and no mutation, migration or selection.
- Confusing chromosome numbers in Down, Turner and Klinefelter syndromes.
- Attributing an experiment to the wrong scientist or the wrong conclusion.
How to practise
Solve every cross twice, once with a Punnett square and once with the product rule, and see if both agree. Do ten mixed problems a week: two crosses, one pedigree, one Hardy-Weinberg sum, one base-sequence question and five recall questions. Keep one-page sheets for the experiments, the disorders and the evolution terms and revise them on the cycle in the NEET revision strategy. Check against real questions with the method in NEET previous year question papers, and read the NCERT chapters line by line using NCERT for NEET.
Using PrepMatic for genetics
PrepMatic's free assessment of about 15 untimed questions shows whether Biology is a weak subject for you, at subject level rather than chapter level. When genetics comes up in your Roadmap, you can check it with a topic test of about 15 questions in 30 minutes, and you can upload your own one-page sheets to generate a mock from them. Full-length mocks that match the paper show how your Biology accuracy holds up under time pressure.
Frequently asked questions
Is genetics important for NEET?
Yes. Genetics and Evolution is a full NMC unit and mixes recall with calculation. Exactly how many questions it gets varies from year to year, so see the tiers in high weightage chapters rather than a fixed count.
How do I solve genetics problems quickly?
Write the parent genotypes, list the gametes, and use the product rule for each gene separately, then multiply. Draw a Punnett square only when the question asks for a full ratio.
Is the lac operon in the NEET syllabus?
The NMC lists Genetics and Evolution as a unit and the lac operon is part of the usual NCERT chapter on the molecular basis of inheritance. Confirm the sub-topics in the NMC PDF.
Which scientists and experiments should I know?
Mendel, Morgan, Griffith, Avery-MacLeod-McCarty, Hershey-Chase, Meselson-Stahl, Chargaff and Watson-Crick for genetics, and Darwin, Lamarck, Oparin-Haldane and Miller-Urey for evolution. Match each to a one-line conclusion.
Are evolution questions mostly theory?
Largely. Evolution questions are usually recall or matching, with an occasional calculation such as a Hardy-Weinberg sum. Learn the definitions and examples exactly as NCERT states them.
Official sources
- National Medical Commission (NMC): the NEET-UG syllabus notified on 22 December 2025.
- NEET-UG official website (NTA): information bulletin, notices and answer keys.
- NCERT: free Class 12 Biology textbooks.
Confirm sub-topics in the latest NMC notification. For the full exam, return to the NEET guide.
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