AP Syllabus focus:
‘When homologous chromosomes or sister chromatids fail to separate, nondisjunction produces gametes that are not haploid.’
Meiosis is usually highly accurate, but errors in chromosome separation can create gametes with abnormal chromosome numbers. These nondisjunction events are a major source of aneuploidy and associated developmental disorders.
What nondisjunction is
Nondisjunction is an error of chromosome segregation during meiosis that causes some gametes to receive too many chromosomes and others too few, rather than being properly haploid.
Nondisjunction: failure of homologous chromosomes (meiosis I) or sister chromatids (meiosis II) to separate correctly during cell division.
Nondisjunction matters because meiosis is meant to halve chromosome number; when it fails, it directly violates the AP focus statement: it “produces gametes that are not haploid.”
Where nondisjunction happens in meiosis
Nondisjunction in meiosis I
In meiosis I, homologous chromosome pairs are supposed to separate to opposite poles.
What fails: homologous chromosomes stay together (do not disjoin) at anaphase I
Immediate result: one daughter cell gets both homologs; the other gets none for that chromosome
After meiosis II: produces two gametes with an extra chromosome and two gametes missing that chromosome (all four gametes abnormal for that chromosome)
Common mechanistic contributors (high-level):
improper spindle attachment to kinetochores
failure to release cohesin at the right time
disrupted alignment at the metaphase plate
Nondisjunction in meiosis II
In meiosis II, sister chromatids are supposed to separate.
What fails: sister chromatids stay together at anaphase II
After meiosis II: produces two normal gametes and two abnormal gametes (one with an extra chromatid/chromosome, one missing it)
Because meiosis II nondisjunction affects only one of the two meiosis I products, fewer gametes are abnormal than in meiosis I nondisjunction (for a single event).

This diagram compares nondisjunction in meiosis I versus meiosis II and shows the resulting gamete chromosome counts. It visually reinforces why meiosis I nondisjunction makes all four gametes abnormal (two and two ), while meiosis II nondisjunction yields two normal gametes plus one and one . Source
Chromosome-number outcomes: aneuploidy
Gametes produced by nondisjunction are not haploid for the affected chromosome.
Aneuploidy: a condition in which a cell has an abnormal number of particular chromosomes (for example, one extra or one missing), rather than an exact multiple of the haploid set.
Aneuploid gametes can form aneuploid zygotes after fertilisation:

This figure illustrates how a nondisjunction event can produce an gamete that, after fertilisation with a normal gamete, forms a (trisomy) zygote. It uses trisomy 21 as an example, making the abstract relationship biologically concrete. Source
gamete + normal gamete → (trisomy) zygote
gamete + normal gamete → (monosomy) zygote
Many aneuploid conceptions do not develop to birth because chromosome imbalance often disrupts gene dosage across many pathways.
Biological significance and key AP takeaways
Nondisjunction is a meiotic segregation error, not a mutation within a gene’s DNA sequence.
It changes chromosome number, which can alter gene dosage (the number of copies of many genes at once).
The AP-essential idea is causal: failure of separation (homologs in meiosis I or sister chromatids in meiosis II) → gametes that are not haploid.
Distinguish the two stages by outcomes:
Meiosis I nondisjunction: all four gametes abnormal (for that chromosome)
Meiosis II nondisjunction: two gametes normal, two abnormal
FAQ
In meiosis I, the error happens before the second division, so both downstream cells inherit the imbalance.
In meiosis II, only one of the two cells from meiosis I is affected.
Alignment can occur with incorrect kinetochore–spindle attachments (e.g., both kinetochores attached to the same pole).
The cell may proceed if checkpoint control is bypassed.
No. The impact depends on which chromosome is affected and the degree of gene-dosage imbalance.
Some aneuploidies are embryonically lethal, while others can be viable.
Karyotyping can visualise whole-chromosome gains or losses.
Fluorescence in situ hybridisation (FISH) can target specific chromosomes for rapid detection.
Yes, mitotic nondisjunction can create somatic mosaicism (different cell lines within one individual).
This differs from meiotic nondisjunction, which directly alters gamete chromosome number.
Practice Questions
State what nondisjunction is and identify one meiotic division in which it can occur. (2 marks)
Defines nondisjunction as failure of chromosomes to separate correctly (1)
States meiosis I (homologous chromosomes) or meiosis II (sister chromatids) (1)
A meiotic error produces four gametes: two are normal and two have abnormal chromosome number for chromosome 7. Explain which meiotic division most likely had nondisjunction and describe how this produces gametes that are not haploid. (5 marks)
Identifies meiosis II as most likely (1)
States sister chromatids fail to separate in anaphase II (1)
Explains one gamete receives both chromatids/extra chromosome () (1)
Explains one gamete receives none for that chromosome () (1)
Notes the other two gametes remain normal/haploid for that chromosome (1)
