Q.In which phase of meiosis are the following formed? Choose the answers from hint points given below.
a. Synaptonemal complex ______
b. Recombination nodules ______
c. Appearance/activation of enzyme recombinase ______
d. Termination of chiasmata ______
e. Interkinesis ______
f. Formation of dyad of cells ______
Hints: 1) Zygotene, 2) Pachytene, 3) Pachytene, 4) Diakinesis, 5) After Telophase-I / before Meiosis-II, 6) Telophase-I / After Meiosis-I.
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🔒 Start your 14-day free trial to unlock the full solution →Concept understanding — Recombination Stage Meiosis
Recombination Stage Meiosis: A First Look
Think of a library where two different encyclopedias sit side by side. Now imagine you could take a few pages from one volume and swap them with the matching pages from the other volume — not copying, but physically exchanging them. That mixing creates new combinations of information that neither book had alone. Recombination stage meiosis does something similar, but with chromosomes, inside living cells.
The Everyday Intuition
You and your sibling both inherit traits from the same parents, yet you are not identical. Why? Because before a sperm or egg is made, the chromosomes from your mother and father get shuffled. Pieces break off and reattach to the other parent's matching chromosome. This is recombination — a deliberate, controlled swap of genetic material. It is nature's way of ensuring that every child is a unique mix, not a carbon copy.
The Precise Meaning
In biology, recombination stage meiosis refers specifically to the phase during meiosis (the cell division that produces gametes — sperm and eggs) where homologous chromosomes — one from each parent — pair up and exchange segments. This happens in prophase I of meiosis, the first of two rounds of division.
The key event is called crossing over. Here is what actually occurs:
- Homologous chromosomes line up side by side, gene by gene.
- At points called chiasmata (singular: chiasma), the chromosomes physically break.
- The broken ends rejoin, but to the other parent's chromosome, not the original one.
- The result: each chromosome now carries a blend of maternal and paternal DNA.
Recombination does not create new genes. It creates new combinations of existing genes. That is why siblings can inherit different versions of the same trait from the same parents.
Why It Matters
Recombination is one of the two main sources of genetic variation in sexually reproducing organisms (the other being the random assortment of chromosomes during meiosis). Without it, offspring would be near-identical to one parent or the other. With it, every gamete is genetically unique.
For a commerce or humanities student, think of it like this: if genes were playing cards, recombination is the dealer shuffling the deck before each hand. The cards themselves do not change, but the order and pairing are different every time. That is why no two people (except identical twins) have the same genetic hand.
What the NCERT Textbook States
The NCERT Class 11 Biology textbook (Chapter 10, Cell Cycle and Cell Division) describes recombination as occurring during pachytene, a substage of prophase I. It states:
- Crossing over involves the exchange of genetic material between non-sister chromatids of homologous chromosomes.
- The enzyme-mediated breakage and rejoining of DNA strands is precise — no genetic material is lost.
- The number of chiasmata varies, but at least one per chromosome pair is typical.
Recombination is not random damage. It is a tightly regulated process. The cell uses specific enzymes to cut, swap, and reseal DNA. Mistakes here can lead to chromosomal abnormalities, which is why the process is so carefully controlled. …
Each of these chromosomal events belongs to a specific, named sub-stage of meiosis, following the sequence of prophase I through to the start of meiosis II.
- a. Synaptonemal complex — Zygotene, when homologous chromosomes pair through synapsis and this protein structure assembles between them.
- b. Recombination nodules — Pachytene, when these points of crossing over appear along the paired chromosomes.
- c. Appearance/activation of the enzyme recombinase — Pachytene, since it is the enzyme that carries out crossing over at this stage.
- d. Termination of chiasmata — Diakinesis, when the chiasmata slide toward the ends of the chromosomes. …
Each event maps onto a specific stage of meiosis I's elaborate prophase or its immediate aftermath: synapsis and recombination events cluster in zygotene and pachytene, chiasma resolution happens in diakinesis, and the dyad of cells forms by telophase I, with interkinesis bridging into meiosis II.
Prophase I of meiosis is unusually long and is split into five distinct sub-stages, and several of the listed events belong specifically to this sequence:
- a. Synaptonemal complex — Zygotene. During zygotene, homologous chromosomes begin coming together in pairs through a process called synapsis, and this pairing is accompanied by the assembly of an elaborate protein structure between the paired partners, the synaptonemal complex.
- b. Recombination nodules — Pachytene. By pachytene, each paired bivalent is resolved into its four chromatids, and the defining feature of this stage is the appearance of recombination nodules — the specific points along the paired chromosomes where crossing over takes place.
- c. Appearance/activation of recombinase — Pachytene. Crossing over, which occurs at these same recombination nodules during pachytene, is an enzyme-driven process carried out by the enzyme recombinase.
- d. Termination of chiasmata — Diakinesis. Diakinesis, the last sub-stage of prophase I, is characterised by terminalisation of chiasmata, in which these X-shaped connections slide toward the ends of the chromosomes. …
Step 1 — List each event with what you know about prophase I's five sub-stages (leptotene, zygotene, pachytene, diplotene, diakinesis) plus the interval after telophase I.
Step 2 — Match each event to its defining sub-stage:
- Synaptonemal complex assembles as chromosomes pair up → this pairing (synapsis) is the hallmark of zygotene.
- Recombination nodules and the recombinase enzyme both belong to the crossing-over machinery, the defining feature of pachytene.
- Chiasmata terminalisation (sliding to chromosome ends) is the hallmark of the last prophase-I sub-stage, diakinesis. …
- TG EAPCET 2026Set ap-2026-05-04-FN1 markMCQQ.In Messelson – Stahl’s experiment if DNA of E.coli is extracted after 40 minutes what will be the densities of DNA molecules formed. (2nd generation) (A) 25% hybrid and 75% light (B) 75% hybrid and 25% light (C) 40% hybrid and 60% light (D) 50% hybrid and 50% light
›Reveal solutionSolution
In Meselson–Stahl’s experiment, after two complete generations (40 minutes for E. coli), the DNA molecules are 50% hybrid (intermediate density) and 50% light (fully N¹⁴) — option (D).
The Meselson–Stahl experiment is the classic proof that DNA replication is semiconservative. The key idea: each parent strand stays intact and acts as a template for a new complementary strand. So after every round of replication, each daughter DNA molecule gets one old strand and one newly made strand.
E. coli was first grown in heavy nitrogen (¹⁵N) until all its DNA was heavy. Then it was shifted to light nitrogen (¹⁴N) and allowed to replicate. The generation time of E. coli is about 20 minutes, so 40 minutes means two full rounds of replication — the second generation.
Let’s trace the densities step by step.
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Start (0 minutes): All DNA is heavy–heavy (¹⁵N/¹⁵N). Only one band at the bottom of the density gradient.
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After 20 minutes (first generation): Each heavy strand gets a light partner. Every molecule is now hybrid (¹⁵N/¹⁴N) — one heavy, one light. So 100% hybrid, 0% light.
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After 40 minutes (second generation): The hybrid molecules from step 2 replicate. Each hybrid molecule separates its two strands. The heavy strand makes a light partner → one hybrid molecule. The light strand makes another light partner → one light–light molecule. So from each hybrid parent, you get one hybrid and one light daughter. …
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- TG EAPCET 2024Set ap-2024-05-08-FN1 markMCQQ.The percentage of ‘ab’ genotype gametes produced by ‘AaBb’ parent plant is (A) 50 (B) 25 (C) 12.5 (D) 75
›Reveal solutionSolution
The 'AaBb' parent produces gametes where alleles for different genes assort independently. The probability of an 'ab' gamete is the product of the probabilities of getting 'a' and 'b', resulting in 25%.
When a parent plant with genotype 'AaBb' produces gametes, it follows the principles of Mendelian genetics, specifically the Law of Independent Assortment. This law states that alleles for different genes (like 'A/a' and 'B/b' in this case) segregate independently of each other during gamete formation. This means that the inheritance of an allele for one gene does not influence the inheritance of an allele for another gene.
A gamete is a reproductive cell that contains only one allele for each gene. Since the parent is diploid (has two alleles for each gene), it must contribute one allele from each pair to its haploid gametes.
Here's how to determine the percentage of 'ab' genotype gametes:
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Identify the alleles for each gene:
The parent plant has the genotype 'AaBb'. This means it is heterozygous for two different genes.
- For the first gene, the alleles are 'A' and 'a'.
- For the second gene, the alleles are 'B' and 'b'.
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Determine the types and proportions of gametes for each gene independently:
- From the 'Aa' genotype, the parent can produce two types of gametes with respect to the first gene: 'A' and 'a'. Since there's an equal chance of passing on either allele, 50% of the gametes will carry 'A' and 50% will carry 'a'.
- Similarly, from the 'Bb' genotype, the parent can produce two types of gametes with respect to the second gene: 'B' and 'b'. Again, 50% of the gametes will carry 'B' and 50% will carry 'b'.
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Apply the Law of Independent Assortment to combine alleles:
Since the two genes assort independently, the probability of a gamete receiving a specific allele for the first gene and a specific allele for the second gene is the product of their individual probabilities.
We are looking for gametes with the 'ab' genotype. This means the gamete must receive an 'a' allele from the first gene and a 'b' allele from the second gene.
- Probability of a gamete receiving 'a' = P(a)=21
- Probability of a gamete receiving 'b' = P(b)=21 …
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- TG EAPCET 2023Set ap-2023-05-11-AN1 markMCQQ.Identify the wrong statements among the following. A. Deletions and insertions of base pairs of DNA cause frame shift mutations B. UV radiation cannot trigger frame shift mutation C. The genes linked closely on the same chromosome have more chances of recombination D. Test cross ratio of a dihybrid Mendelian cross would be 1:1 (A) A, B & C (B) B, C & D (C) A, C & D (D) A, B, C & D
›Reveal solutionSolution
Frame-shift mutations arise from indels, not UV; closely linked genes recombine less, not more; and a dihybrid test cross yields 1:1:1:1, not 1:1. The wrong statements are B, C and D.
The question tests your understanding of mutation mechanisms, linkage, and Mendelian ratios. Let's examine each statement against the underlying genetics.
Concept: Mutations, Linkage and Test Crosses
Frame-shift mutations occur when the reading frame of codons is disrupted—insertions or deletions (indels) that are not multiples of three shift every downstream codon. UV radiation typically causes point mutations (thymine dimers), not frame shifts.
Linkage means genes sit on the same chromosome. The closer two genes are, the less likely a crossover event will separate them during meiosis—so recombination frequency decreases with proximity.
A test cross (crossing an individual with a homozygous recessive) reveals the gamete types. For a dihybrid (AaBb×aabb), you expect four phenotypic classes in a 1:1:1:1 ratio if the genes assort independently.
Evaluating Each Statement
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Statement A: Deletions and insertions of base pairs cause frame-shift mutations.
This is correct. An indel that is not a multiple of three nucleotides shifts the reading frame from that point onward, altering every subsequent amino acid. This is the textbook definition of a frame-shift mutation.
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Statement B: UV radiation cannot trigger frame-shift mutation.
This is correct. UV light induces thymine dimers—covalent bonds between adjacent thymine bases—which are repaired or lead to base substitutions (point mutations). UV does not insert or delete nucleotides, so it does not cause frame shifts.
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Statement C: Genes linked closely on the same chromosome have more chances of recombination.
This is wrong. Recombination frequency is inversely proportional to the distance between genes. Tightly linked genes (close together) have a lower probability of a crossover occurring between them, hence fewer recombinants. This is the basis of genetic mapping: 1 map unit = 1 % recombination.
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Statement D: Test cross ratio of a dihybrid Mendelian cross would be 1:1.
This is wrong. A dihybrid test cross AaBb×aabb produces four gamete types from the heterozygote (AB,Ab,aB,ab in equal proportions if unlinked), each combining with ab from the tester. The phenotypic ratio is 1:1:1:1 (four classes), not 1:1 (two classes). A 1:1 ratio describes a monohybrid test cross.
Watch outA common mistake is confusing "linked" with "more recombination." Linkage reduces recombination; only unlinked (independent) genes recombine freely at 50 %.
TipRemember: map distance in centiMorgans equals recombination percentage. Close genes → small map distance → low recombination.
Summary Table
Statement Content Verdict A Indels cause frame shifts ✓ Correct B UV cannot cause frame shifts ✓ Correct C Close linkage → more recombination ✗ Wrong D Dihybrid test cross → 1:1 ✗ Wrong -
- TG EAPCET 2023Set ap-2023-05-11-FN1 markMCQQ.The diploid stage in the life cycle of Plasmodium vivax is (A) Sporozoite (B) Cryptozoite (C) Metacryptozoite (D) Ookinete
›Reveal solutionSolution
In Plasmodium vivax, the only diploid stage is the ookinete, formed immediately after fertilization in the mosquito gut; all other stages are haploid. The answer is (D).
The life cycle of malarial parasites alternates between haploid and diploid phases, and understanding where diploidy occurs requires tracing sexual reproduction. Most of the parasite's life is spent as a haploid organism, multiplying asexually in both human and mosquito hosts. Diploidy is brief and tied to a single event: fertilization.
When a female Anopheles mosquito takes a blood meal from an infected human, it ingests gametocytes (the sexual forms). In the mosquito's midgut, these gametocytes mature into gametes—male microgametes and female macrogametes. Fertilization occurs when a microgamete fuses with a macrogamete, producing a zygote. This zygote is the first diploid cell, containing genetic material from both gametes.
The zygote does not remain static. Within hours, it elongates and becomes motile, transforming into an ookinete. This worm-like, motile form penetrates the mosquito's gut wall to form an oocyst on the outer surface. Crucially, the ookinete is still diploid—it is simply the motile, invasive form of the zygote.
Once the oocyst forms, meiosis occurs inside it, restoring the haploid state and producing thousands of sporozoites. From that point forward, all stages (sporozoites, cryptozoites, metacryptozoites, merozoites, gametocytes) are haploid until the next round of fertilization.
Let's examine each option:
- Sporozoite (A): These are the infective forms injected by the mosquito into the human bloodstream. They arise from meiotic division within the oocyst and are haploid. …
- TG EAPCET 2021Set ap-2021-08-09-FN1 markMCQQ.Choose the correct statements from the following. A) Meiosis has to occur if a diploid body has to produce gamets B) In Cladophora it is not possible to categorize the male and female gamets C) Organisms exhibiting external fertilization show greater synchrony between sexes D) In Wolfia isogamets can be seen (A) B, C, D (B) A, B, C (C) A, B, D (D) A, C, D
›Reveal solutionSolution
The question tests knowledge of meiosis, gamete types, and fertilization biology. The correct statements are A, B, and C, so the answer is option (B).
Concept & Intuition
This problem checks your understanding of three core ideas:
- Meiosis is essential for gamete formation in diploid organisms to halve chromosome number.
- Isogamy vs. anisogamy: In some algae like Cladophora, gametes look alike (isogametes), so you cannot label them male/female.
- External fertilization requires precise timing (synchrony) between sexes to increase chances of gamete meeting.
- Wolfia (a tiny flowering plant) produces anisogametes (male and female), not isogametes.
Let’s evaluate each statement step by step.
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Statement A: “Meiosis has to occur if a diploid body has to produce gametes”
- In sexually reproducing diploid organisms, gametes must be haploid.
- Meiosis reduces chromosome number from diploid (2n) to haploid (n).
- Without meiosis, gametes would be diploid, leading to polyploidy upon fusion.
- True — meiosis is mandatory for gamete formation in diploids.
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Statement B: “In Cladophora it is not possible to categorize the male and female gametes”
- Cladophora is a green alga that reproduces by isogamy — gametes are morphologically identical (same size and shape).
- They may have different mating types (+ and –), but you cannot visually distinguish “male” from “female”.
- True — categorization into male/female is not possible based on appearance.
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Statement C: “Organisms exhibiting external fertilization show greater synchrony between sexes”
- External fertilization (e.g., in fish, frogs) occurs in water where gametes are released into the environment. …
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