What Is Codominance in Biology? Definition & Examples

Genetic inheritance is a fundamental biological process through which traits are passed from parents to their offspring. This transmission occurs through genetic material, primarily DNA, which contains all the instructions for an organism’s development and function. Every individual receives a unique combination of genetic information from their biological parents, influencing various characteristics like appearance and certain predispositions. The study of how these traits are passed down forms the basis of genetics, revealing the intricate mechanisms that shape life.

What is Codominance?

Codominance is a genetic pattern where two different versions of the same gene, known as alleles, are expressed simultaneously and equally in an organism. In a heterozygous individual, both alleles contribute distinctly to the observable characteristic, or phenotype. This means that neither allele masks the other; instead, both are fully visible.

Unlike situations where one allele might be dominant and fully override the effect of a recessive allele, in codominance, there is no masking. The resulting phenotype is not a blend or an intermediate form, but rather a clear display of both traits at the same time. This direct and equal expression distinguishes codominance as a unique pattern of inheritance.

How Codominance Differs from Other Inheritance Patterns

Understanding codominance is clearer when compared to other common inheritance patterns, such as complete dominance and incomplete dominance. In complete dominance, one allele completely masks the expression of the other allele in a heterozygous individual. For example, if an allele for a particular trait is dominant, its characteristic will be the only one observed, even if a recessive allele is also present.

Incomplete dominance presents a different scenario, where the heterozygous phenotype is an intermediate blend of the two homozygous phenotypes. Neither allele is fully dominant, leading to a mixed appearance. A classic example is a cross between red and white flowers producing pink offspring, as the colors seem to blend.

Codominance differs because both alleles are simultaneously and distinctly expressed in the heterozygote, without any blending or masking. While incomplete dominance results in a new, intermediate phenotype, codominance allows both original traits to be visibly present.

Real-World Instances of Codominance

One prominent example of codominance in humans is the ABO blood group system. This system involves three alleles: IA, IB, and i. The IA allele leads to the production of A antigens on red blood cells, and the IB allele results in B antigens. When an individual inherits both the IA and IB alleles, they express both A and B antigens equally on their red blood cells, resulting in AB blood type.

Another illustration of codominance is observed in the coat color of roan cattle or horses. A roan animal possesses both red and white hairs, which are distinctly present across its coat. This is not a blended pink color, but rather a mixture of individual red hairs and individual white hairs. The alleles for red and white coat colors are both fully expressed, contributing to the speckled appearance.

Similarly, the MN blood group system in humans also demonstrates codominance. Individuals who are heterozygous for the M and N alleles (LMLN genotype) will have both M and N antigens present on the surface of their red blood cells.

The Underlying Genetic Expression

The mechanism behind codominance involves both alleles producing functional gene products. These products, often specific proteins or enzymes, are then expressed in the organism. For example, in the ABO blood group system, the IA and IB alleles each produce different enzymes that modify antigens on the surface of red blood cells.

Because both alleles are actively producing their respective products, both associated traits become visible in the phenotype. This contrasts with dominant-recessive relationships where the recessive allele typically produces a non-functional or less effective product, or its expression is simply overwhelmed by the dominant allele’s product.