Sex determination
XY system: humans, Drosophila — male XY, female XX. ZW: birds — female ZW, male ZZ. Haplodiploidy: bees — male haploid (parthenogenesis), female diploid. Y-chromosome carries SRY gene.
-- NCERT Class 12 Biology, Ch. 4, p. 84The trap that costs marks in sex-linked inheritance questions: confusing carrier status with affected status in females for X-linked recessive conditions.
Sex determination in humans follows the XX-XY system. Females carry two X chromosomes (XX); males carry one X and one Y (XY). The father's gamete determines the sex of offspring — X-bearing sperm produces daughters, Y-bearing sperm produces sons. The Y chromosome carries the SRY gene (sex-determining region), which triggers male development (NCERT Class 12 Biology Chapter 4, page 84).
Sex-linked inheritance refers to genes located on sex chromosomes. Most NEET-relevant examples involve X-linked recessive traits: haemophilia, colour-blindness, and Duchenne muscular dystrophy.
The critical inheritance logic:
The high-frequency trap: When a pedigree shows an affected male, students incorrectly conclude his daughters will also be affected. They forget that the daughter receives a normal X from her mother (assuming mother is homozygous dominant), making the daughter a carrier only. The recessive allele on one X is masked by the dominant allele on the other.
Watch-out for NEET: Questions often present a cross between a carrier female and a normal male, then ask for the probability of an affected child. The answer is 1/4 of sons (not 1/4 of all children) — because only males express the single-copy recessive.
Select an option to see the explanation. Wrong answers show why your choice was tempting — and name the exact trap it exploits.
In humans, sex of the offspring is determined by:
Haemophilia is an X-linked recessive disorder. A carrier woman marries a normal man. What proportion of their SONS will be affected?
A colour-blind man marries a woman who is homozygous normal for colour vision. What is the genotype of their daughters?
In the XX-XY system of sex determination, which parent contributes the sex-determining chromosome to produce a male offspring?
A haemophilic man (X^h Y) marries a carrier woman (X^H X^h). What is the probability that their daughter will be haemophilic?
Which of the following statements about X-linked recessive disorders is CORRECT?
In a cross between a carrier female for colour-blindness (X^C X^c) and a normal male (X^C Y), what fraction of ALL offspring will be colour-blind?
The SRY gene responsible for male sex determination in humans is located on:
Given
A woman who is a carrier for haemophilia (X^H X^h) marries a normal man (X^H Y).
Required
(a) Probability of a haemophilic child. (b) Probability of a haemophilic son. (c) Probability that a randomly chosen son is haemophilic.
Concept
X-linked recessive inheritance. Males express recessive allele on single X. Females need homozygous recessive to express.
Formula/Logic
Punnett square for X-linked cross. Each gamete combination is equally probable (1/4 each).
Substitution
| | X^H (from father) | Y (from father) | |---|---|---| | X^H (from mother) | X^H X^H (normal daughter) | X^H Y (normal son) | | X^h (from mother) | X^H X^h (carrier daughter) | X^h Y (haemophilic son) |
Calculation
- Four equally likely outcomes: X^H X^H, X^H X^h, X^H Y, X^h Y. - Affected offspring: only X^h Y = 1/4 of all children. - Among sons only (X^H Y and X^h Y): affected = 1/2 of sons. - Among daughters: 0 affected (one is carrier, but not affected).
Final answer
(a) P(haemophilic child) = 1/4 (b) P(haemophilic son being born) = 1/4 (same as (a) since only sons can be affected here) (c) P(a son is haemophilic | child is son) = 1/2
Common trap
Students confuse (a) and (c). "What fraction of sons are affected?" = 1/2. "What is the probability of an affected child?" = 1/4. The word "son" as a condition changes the denominator. This is the X-linked inheritance carrier-vs-affected confusion at its most exam-costly.
Similar NEET-style question
A colour-blind woman (X^c X^c) marries a man with normal vision (X^C Y). What proportion of their children will be colour-blind? [Answer: 1/2 — all sons (X^c Y) are affected, all daughters (X^C X^c) are carriers. Sons = half of all children.] ---
XY system: humans, Drosophila — male XY, female XX. ZW: birds — female ZW, male ZZ. Haplodiploidy: bees — male haploid (parthenogenesis), female diploid. Y-chromosome carries SRY gene.
-- NCERT Class 12 Biology, Ch. 4, p. 84F2 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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