D3.2.19 (HL)—Autosomal gene linkage
Autosomal gene linkage occurs when genes on the same non-sex chromosome tend to be inherited together unless crossing over separates them.
- Syllabus
- First assessment 2025
- Objective
- D3.2.19
- Level
- HL
Autosomal gene linkage occurs when genes on the same non-sex chromosome tend to be inherited together unless crossing over separates them.

Coverage 2013–2025 · Updated 16 Jul 2026
| Same AaBb genotype | Alleles on one homolog | Alleles on the other | Name |
|---|---|---|---|
| AB/ab | A with B | a with b | coupling phase |
| Ab/aB | A with b | a with B | repulsion phase |
Writing only AaBb records which alleles are present but loses which combinations share a chromosome. For linked genes, parental phase determines which gametes are common and which require crossing over.
Autosomal linkage means two loci share a non-sex chromosome. Sex linkage is different: it refers to a locus on a sex chromosome, usually X.

Start with a heterozygote in coupling phase: parental homologs carry AB and ab. After DNA replication, each homolog has two sister chromatids.
A chiasma between the A and B loci exchanges matching segments between non-sister chromatids. Two chromatids remain parental, while two become Ab and aB.
| Chromatid or gamete class | Allele combination | Origin |
|---|---|---|
| parental | AB and ab | no exchange between the loci |
| recombinant | Ab and aB | crossover between the loci |
A crossover elsewhere on the chromosome does not recombine these two loci. The exchange must occur between their positions to separate their parental allele combination.
Cross AB/ab with ab/ab. Because the tester contributes only ab, each offspring's phenotype or genotype identifies the gamete produced by the double heterozygote.
| Heterozygote gamete | Offspring | Classification for AB/ab parent |
|---|---|---|
| AB | AaBb | parental |
| ab | aabb | parental |
| Ab | Aabb | recombinant |
| aB | aaBb | recombinant |
Classify by comparison with the heterozygous parent's chromosome combinations, not by whether an offspring looks common or unusual in the population.
r=NR×100%
Here, R is the number of recombinant offspring and N is the total. If a test cross gives 420 AB, 400 ab, 90 Ab and 90 aB offspring, r = (90 + 90) / 1000 × 100% = 18%.
| Observation | Inference |
|---|---|
| recombinants much below 50% | loci are linked |
| lower recombinant frequency | loci are usually closer, so fewer chiasmata fall between them |
| about 50% recombinants | loci behave as unlinked; they may be on different chromosomes or far apart |
Recombinant frequency does not exceed 50% in an ordinary two-locus test. Multiple crossovers can restore parental combinations, so frequency underestimates large physical distances.
meiosis predicts gamete combinations → chromosome loci determine whether genes assort independently or travel together → crossing over creates reciprocal recombinants → test-cross counts reveal parental phase and recombinant frequency → chi-squared tests whether departures from a chosen ratio exceed chance expectation
| Offspring pattern | First model to examine |
|---|---|
| 9:3:3:1 F2 | two unlinked genes with complete dominance |
| 1:1:1:1 test cross | four equally frequent gametes from an unlinked double heterozygote |
| two large and two small reciprocal test-cross classes | linked loci with crossing over |
| significant χ² departure | assumptions, linkage, viability, fertilization or scoring require review |
Keep prediction and evidence separate: define the genetic model first, calculate expected counts from it, compare observations with the expectation, and change the model only when chromosome location or statistical evidence requires it.
[ 3 ]
Outline how it can be shown that the genes for shell base colour (Cc) and presence or absence of bands (Bb) are linked.