DNA structure
Watson-Crick double helix: antiparallel strands; A=T (2 H-bonds), G≡C (3 H-bonds); 10 bp/turn; pitch 3.4 nm; diameter 2 nm. Chargaff's rule: A=T, G=C. Z-DNA, A-DNA, B-DNA forms.
-- NCERT Class 12 Biology, Ch. 5, p. 94NEET regularly tests whether you can distinguish the structural features of DNA from RNA and recall the details of the Watson-Crick model. The high-frequency trap here is confusing the directionality and bonding specifics — getting the strand polarity, base-pairing rules, or groove nomenclature wrong costs marks under negative marking.
The Watson-Crick model (1953) describes DNA as a right-handed double helix with two antiparallel polynucleotide strands. "Antiparallel" means one strand runs 5'→3' while its complement runs 3'→5'. The strands are held together by hydrogen bonds between complementary bases: adenine pairs with thymine via two H-bonds (A=T), and guanine pairs with cytosine via three H-bonds (G≡C). This is Chargaff's rule in structural form — the molar ratio of A/T and G/C each equals 1 (NCERT Class 12 Biology Chapter 5, page 94).
The backbone consists of alternating deoxyribose sugar and phosphate groups linked by 3'–5' phosphodiester bonds. The bases project inward, stacked 0.34 nm apart; one full turn spans 3.4 nm and contains approximately 10 base pairs. The helix has a major groove and a minor groove — proteins that read DNA (transcription factors, regulatory proteins) typically interact via the major groove, where more of the base-pair's chemical identity is exposed.
DNA vs RNA — the four structural differences NEET expects:
| Feature | DNA | RNA |
|---|---|---|
| Sugar | Deoxyribose (–H at 2' carbon) | Ribose (–OH at 2' carbon) |
| Bases | A, T, G, C | A, U, G, C |
| Strands | Double-stranded (usually) | Single-stranded (usually) |
| Stability | More stable (no 2'–OH) | Less stable, more reactive |
Thymine in DNA is replaced by uracil in RNA — both pair with adenine, but uracil lacks the methyl group at the 5-position.
Watch-out for NEET: when a question says "which base is absent in RNA," the answer is thymine, not uracil. Reversing this is a common negative-marking loss.
Select an option to see the explanation. Wrong answers show why your choice was tempting — and name the exact trap it exploits.
The distance between two adjacent base pairs in the B-form DNA double helix is:
The number of hydrogen bonds between adenine and thymine in a DNA double helix is:
Which of the following bases is present in RNA but absent in DNA?
A DNA molecule has 30% adenine. What is the percentage of guanine in the same molecule?
A DNA molecule contains 600 base pairs. How many complete helical turns does it have in B-form?
The two strands of a DNA double helix are described as antiparallel because:
DNA is more stable than RNA under physiological conditions. Which structural feature of DNA primarily accounts for this greater stability?
Regulatory proteins that need to read the DNA sequence without unwinding the helix typically bind at:
Given
A double-stranded DNA molecule has 1,000 base pairs. Analysis of one strand shows: A = 200, T = 150, G = 350, C = 300.
Required
Find the base composition (number of each base) of the complementary strand and the complete molecule.
Concept
In double-stranded DNA, adenine on one strand pairs with thymine on the complementary strand, and guanine pairs with cytosine (Watson-Crick base-pairing). Chargaff's rule ensures that for the whole molecule, A = T and G = C.
Formula/Rule
Complementary strand base = partner of the given strand base: - A in given strand → T in complementary strand - T in given strand → A in complementary strand - G in given strand → C in complementary strand - C in given strand → G in complementary strand
Substitution
Complementary strand: - T (paired with A = 200) = 200 - A (paired with T = 150) = 150 - C (paired with G = 350) = 350 - G (paired with C = 300) = 300
Calculation
Whole molecule totals: - Total A = 200 (strand 1) + 150 (strand 2) = 350 - Total T = 150 (strand 1) + 200 (strand 2) = 350 ✓ (A = T) - Total G = 350 (strand 1) + 300 (strand 2) = 650 - Total C = 300 (strand 1) + 350 (strand 2) = 650 ✓ (G = C) - Grand total = 350 + 350 + 650 + 650 = 2,000 bases = 1,000 base pairs ✓ Note: the counts 200, 150, 350, 300, and 1,000 are exact counting integers — they do not involve significant-figure considerations.
Final answer
Complementary strand: A = 150, T = 200, G = 300, C = 350. Whole molecule: A = T = 350; G = C = 650. Total = 2,000 bases.
Common trap
Students sometimes apply Chargaff's rule to a single strand (expecting A = T within that strand). Chargaff's rule applies to the double-stranded molecule as a whole. In a single strand, A ≠ T and G ≠ C is perfectly normal.
Similar NEET-style question
"If one strand of DNA has the base composition A : T : G : C = 20% : 30% : 15% : 35%, what is the base composition of the complete double-stranded DNA molecule?" (Apply the same complementary-pairing logic, then average across both strands.) ---
Watson-Crick double helix: antiparallel strands; A=T (2 H-bonds), G≡C (3 H-bonds); 10 bp/turn; pitch 3.4 nm; diameter 2 nm. Chargaff's rule: A=T, G=C. Z-DNA, A-DNA, B-DNA forms.
-- NCERT Class 12 Biology, Ch. 5, p. 94F2 ratio in monohybrid cross — products of independent assortment of two alleles per locus.
| Symbol | Quantity | SI Unit |
|---|---|---|
| ratio | F2 progeny ratio | - |
F2 ratio in dihybrid cross with two independently-segregating loci, complete dominance, no linkage.
| Symbol | Quantity | SI Unit |
|---|---|---|
| ratio | F2 phenotype ratio | - |
In an idealised population (no mutation, drift, selection, gene flow, random mating), allele and genotype frequencies remain constant.
| Symbol | Quantity | SI Unit |
|---|---|---|
| p | freq of dominant allele A | - |
| q | freq of recessive allele a | - |
Proportion of recombinant offspring measures genetic distance between linked loci. Capped at 50% (independent assortment).
| Symbol | Quantity | SI Unit |
|---|---|---|
| RF | recombination frequency | % |
These are the exact patterns that cause wrong answers in NEET. Each trap includes when it triggers and how to avoid it.
Category: Sign Convention
DNA polymerase synthesises only 5'→3'. Leading strand: continuous, same direction as fork. Lagging: discontinuous (Okazaki), opposite to fork.
Question on Okazaki, leading vs lagging, primer direction.
Reading template 3'→5'; synthesising 5'→3'. Lagging strand needs short fragments because it can't run continuously against fork direction.
Category: Negative Marking
Five forces disturb HW: mutation, gene flow, drift, selection, non-random mating. ANY of these violates equilibrium.
Question asks which factor maintains/disturbs HW.
Random mating + no other forces → equilibrium. ANY of mutation/migration/drift/selection/assortative mating → disequilibrium.
Category: Similar Terms
Monohybrid: genotype 1:2:1 (AA:Aa:aa); phenotype 3:1.
Question asks for one ratio while presenting cross details.
Always note dominance: phenotype merges Aa + AA; genotype keeps them separate.
Category: Similar Terms
X-linked recessive (haemophilia, colour-blindness): affects males predominantly; carrier mother → 50% sons affected; affected father → all daughters carriers but not affected.
Pedigree question; carrier vs affected.
Sex chromosomes: XX vs XY. Recessive on X needs both copies (XaXa) in female, only one (XaY) in male.
Category: Similar Terms
Allopatric: geographic isolation. Sympatric: same area, no physical barrier (e.g. polyploidy in plants, host-shift).
Question gives speciation scenario and asks which type.
If geographic barrier mentioned → allopatric. If population overlaps → sympatric.
Root cause: formula misuse
Genotype frequencies: p² (AA) + 2pq (Aa) + q² (aa) = 1. Allele frequencies: p + q = 1. Don't drop 2pq.
Root cause: concept gap
ALL DNA pol synthesises 5'→3'. Lagging strand uses Okazaki fragments to APPEAR to extend toward fork while each fragment grows 5'→3'.
Root cause: concept gap
Frameshift = ANY indel NOT divisible by 3 (since codons are triplets). Indels of 3, 6, 9... preserve reading frame.
Root cause: term confusion
Start codon: AUG (Met / fMet). Stop codons: UAA (ochre), UAG (amber), UGA (opal/umber).
51 questions from NEET 2020, 2021, 2022, 2023, 2024, 2025. Answers verified against NTA official keys.
Identify the statement that is NOT correct.
Which factor is important for termination of transcription?
What is the pattern of inheritance for polygenic trait?
Which of the following statement is correct regarding the process of replication in E.coli?
Which one of the following factors will not affect the Hardy-Weinberg equilibrium?
The phenomenon of pleiotropism refers to
What is the role of RNA polymerase III in the process of transcription in Eukaryotes?
Among eukaryotes, replication of DNA takes place in :
Expressed Sequence Tags (ESTs) refers to
Unequivocal proof that DNA is the genetic material was first proposed by
Broad palm with single palm crease is visible in a person suffering from-
Select the correct group/set of Australian Marsupials exhibiting adaptive radiation.
XO type of sex determination can be found in :
The process of translation of mRNA to proteins begins as soon as :
Which of the following occurs due to the presence of autosome linked dominant trait ?
Detritivores breakdown detritus into smaller particles. This process is called:
If the length of a DNA molecule is 1.1 metres, what will be the approximate number of base pairs?
Which of the following is not a desirable feature of a cloning vector?
Mutations in plant cells can be induced by: 130. Match List-I with List-II.
Which of the following RNAs is not required for the synthesis of protein?
•ŸÈ‹ πŸ ∑ § ‚◊ÿ «UË.∞Ÿ.∞. ∑§Ë ∑È §«U‹Ë ∑§Ê πÊ ‹Ÿ ◊ ∑§ÊÒŸ‚Ê
Recurring question shapes from past papers. Each pattern shows why wrong options look tempting.
similar term confusion
Biology relies on precise terminology; close terms tempt selection.
Test yourself on this topic with real past-paper questions:
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