What Is the Difference Between a Gene and an Allele?

Genetics is the field of biology dedicated to studying heredity and the mechanisms by which biological information is transferred from one generation to the next. Understanding how traits are passed down requires a clear grasp of the fundamental units of inheritance. Genes and alleles are often mentioned together, yet they represent distinct layers of hereditary instruction. This article clarifies the precise differences between a gene and an allele.

Understanding the Gene

A gene is the basic physical and functional unit of heredity. It consists of a specific sequence of deoxyribonucleic acid (DNA), or sometimes ribonucleic acid (RNA), which contains the instructions for making a functional product, typically a protein. These protein products perform the majority of tasks necessary for an organism to function, determining everything from metabolism to physical characteristics.

Each gene occupies a fixed position on a chromosome, a location known as its locus. The gene represents the inherited instruction for a broad category of a trait, such as “eye color” or “seed shape.” The instruction is a segment of DNA that can vary in size from a few hundred to over two million base pairs.

Understanding the Allele

An allele, in contrast, is a specific variant or form of a gene. While the gene sets the stage for a trait like flower color, the allele dictates the actual expression, such as red or white. Alleles are variations in the DNA sequence at a gene’s locus, arising through mutation. These slight differences in the sequence account for the observable variation within a species.

A population can possess multiple different alleles for a single gene, leading to greater diversity in traits.

The Gene-Allele Relationship

The relationship between a gene and an allele is hierarchical, with the gene being the abstract category or location, and the allele being the concrete version of that instruction. The gene is the fixed address on the chromosome, while the allele is the specific structure built at that address. For instance, the gene for the ABO blood group is the fixed instruction set, but the \(I^A\), \(I^B\), and \(i\) variants are the different alleles that exist within the human population for that gene.

Most complex organisms, including humans, are diploid, meaning they carry two sets of chromosomes—one inherited from each parent. This means that for every gene, an individual possesses two alleles, which reside at the same locus on homologous chromosomes. These two inherited alleles may be identical, or they may be different from one another.

This pairing of alleles is the mechanism that generates individual genetic makeup, known as the genotype. The gene provides the potential for a trait, and the two alleles determine the specific outcome observed in the individual. The distinction is that the gene is the template for the entire species, while the combination of alleles is unique to the individual.

How Alleles Determine Inherited Traits

The combination of the two alleles an individual possesses for a given gene determines the physical manifestation of the trait, called the phenotype. When an individual inherits two identical alleles for a gene, they are said to be homozygous for that trait. Conversely, inheriting two different alleles makes the individual heterozygous.

The interaction between these two alleles dictates which version of the trait is expressed, following specific patterns of inheritance. In a simple model, one allele can be dominant, meaning its associated trait will be expressed even if only one copy is present. The other allele is recessive, and its trait will only appear if the individual is homozygous, possessing two copies of the recessive allele.

For example, the allele for brown eyes can be dominant over the allele for blue eyes. A person only needs one brown-eye allele to have brown eyes, but must inherit two blue-eye alleles to express the blue-eye phenotype. These interactions, first described by Gregor Mendel, demonstrate how the specific pairing of alleles translates the genetic code into observable characteristics.