Meiosis & Genetic Variation
Meiosis takes a diploid (2n) cell through one round of DNA replication and two divisions, producing four genetically unique haploid (n) gametes. Variation arises from crossing over, independent assortment, and random fertilization.
Meiosis I — reductional (separates homologs)
- Prophase I: chromosomes condense; homologs pair (synapsis) forming tetrads (bivalents); crossing over occurs at chiasmata. Major source of genetic variation.
- Metaphase I: tetrads line up at the metaphase plate; independent assortment of homologous pairs — each pair orients independently → 2ⁿ combinations of maternal/paternal chromosomes (2²³ ≈ 8.4 million in humans, before crossing over).
- Anaphase I: homologous chromosomes separate; sister chromatids stay together.
- Telophase I / Cytokinesis: two haploid cells, each chromosome still as sister chromatid pair.
Meiosis II — equational (separates sister chromatids)
- Resembles mitosis. No DNA replication occurs between Meiosis I and II.
- Sister chromatids separate at anaphase II.
- Result: 4 haploid cells, each genetically distinct.
Mitosis vs. Meiosis (high-yield comparison)
| Feature | Mitosis | Meiosis |
|---|---|---|
| Divisions | 1 | 2 |
| Daughter cells | 2 | 4 |
| Ploidy | 2n → 2n | 2n → n |
| Synapsis / crossing over | No | Yes (Prophase I) |
| Genetic identity | Identical to parent | Genetically unique |
| Purpose | Growth, repair, asexual reproduction | Gamete formation |
Sources of genetic variation
- Crossing over (Prophase I) — exchanges segments between homologs at chiasmata.
- Independent assortment (Metaphase I) — random orientation of tetrads.
- Random fertilization — any sperm × any egg.
- Mutation — the ultimate source of new alleles. The other three only shuffle existing variation.
Linked vs. unlinked genes
- Unlinked (different chromosomes): independent assortment — predicted dihybrid 9:3:3:1.
- Linked (same chromosome): tend to inherit together; recombination only occurs via crossing over. Recombination frequency (RF) ≤ 50%; 1% RF ≈ 1 map unit (centimorgan). Closer genes → fewer recombinants.
Nondisjunction
- Failure of chromosomes (Meiosis I) or sister chromatids (Meiosis II) to separate.
- Results in aneuploidy: one gamete has n+1 chromosomes, another has n−1.
- Examples in humans: Trisomy 21 (Down syndrome), XXY (Klinefelter), XO (Turner), XXX, XYY.
Example questions
MCQ During which phase do tetrads form and crossing over occur? (A) Prophase I (B) Metaphase I (C) Prophase II (D) Anaphase II
Answer: A. Synapsis pairs homologs into tetrads (bivalents) during Prophase I; crossing over occurs at the chiasmata that form between non-sister chromatids of homologous chromosomes.
FRQ Explain how meiosis generates genetic variation, and describe how this variation contributes to evolution by natural selection.
Answer: Meiosis generates variation through (1) crossing over in Prophase I, which recombines alleles between homologs; (2) independent assortment in Metaphase I, in which each homologous pair orients randomly, producing 2ⁿ combinations of maternal/paternal chromosomes; and (3) random fertilization, which combines two genetically unique gametes. This raw variation supplies the heritable phenotypic differences on which natural selection acts: individuals whose variants confer higher fitness reproduce more, gradually changing allele frequencies in the population over generations.
MCQ Two genes are 18 map units apart. From a test cross, what percent recombinant offspring are expected? (A) 9% (B) 18% (C) 36% (D) 50%
Answer: B. A map unit (centimorgan) is defined as 1% recombination, so genes 18 map units apart yield 18% recombinant offspring in a test cross.