How Gene Evolution Works: From Mutation to New Functions
Explore the processes driving the evolution of life's code, from small-scale variations to the emergence of complex, interconnected biological functions.
Explore the processes driving the evolution of life's code, from small-scale variations to the emergence of complex, interconnected biological functions.
Gene evolution describes how the genetic composition of populations shifts across generations, leading to new traits and species. Genes are the specific segments of DNA that function as the basic units of heredity, containing the instructions for building and operating an organism. This evolution is not a directed event but an interplay of random changes and environmental pressures, shaping how organisms adapt and diversify.
The source of all new genetic material is mutation, a random change in the DNA sequence. These changes are the raw materials for evolution, introducing new versions of genes, called alleles, into a population. They can arise from errors during DNA replication or environmental damage. While some mutations can be harmful, many have no immediate effect, and a few might produce a beneficial trait.
There are several types of mutations that can alter a gene’s instructions. Point mutations involve a change in a single DNA base. Other mutations involve the insertion or deletion of one or more DNA bases; an insertion adds new genetic material, while a deletion removes it. These changes provide the genetic novelty upon which other evolutionary forces can act.
Once genetic variation arises, several forces shape the frequencies of new alleles within a population, sorting existing variations. The primary force is natural selection, a non-random process that favors traits enhancing an organism’s ability to survive and reproduce. Individuals with advantageous traits are more likely to pass their genes on, causing these beneficial alleles to increase in frequency.
Genetic drift involves random fluctuations in allele frequencies due to chance events, and its effects are not related to a trait’s usefulness. Its impact is most pronounced in small populations, where chance can have a large effect on the genetic makeup. For instance, the alleles carried by the few individuals that happen to reproduce will become more common, regardless of their adaptive value.
Gene flow is the transfer of genetic material between populations through migration. When individuals move to a new population and interbreed, they introduce their alleles into the new group. This process can introduce new genetic variants or change the proportions of existing ones. Sustained gene flow can make separate populations more genetically similar, counteracting the diversifying effects of selection and drift.
Entirely new genes can be created, providing a source of evolutionary innovation. The most common mechanism is gene duplication, where a mistake during cell division results in an extra copy of a gene. This redundancy frees one copy from its original function, allowing it to accumulate mutations without harming the organism.
A duplicated gene has several possible fates. One outcome is neofunctionalization, where the new copy acquires enough mutations to perform a completely new function, which is a powerful way for organisms to evolve new capabilities. For instance, a duplicated digestive gene could evolve to help detoxify a poison.
Another fate is subfunctionalization, where the original gene had multiple functions, and each copy specializes in a subset of those roles. This division of labor can lead to more refined performance of each function. A final possibility is pseudogenization, where the duplicated gene accumulates disabling mutations and becomes non-functional.
Scientists trace gene evolution by comparing the genomes of different species using comparative genomics. This field allows researchers to identify shared genes, deduce evolutionary relationships, and reconstruct evolutionary events by analyzing DNA sequences.
Two concepts in this analysis are orthologs and paralogs. Orthologs are genes in different species that originated from a single gene in their last common ancestor, reflecting their shared ancestry. These genes were separated by a speciation event and retain the same function, such as the hemoglobin gene in humans and chimpanzees.
Paralogs are genes within the same species that arose from a gene duplication event. These genes form “gene families” with related but distinct functions. For example, the human globin gene family includes myoglobin, which stores oxygen in muscles, and hemoglobin subunits, which transport oxygen in blood. Both arose from a single ancestral gene that duplicated and diverged.
Genes do not evolve in isolation and often evolve in response to one another through coevolution. This process occurs when two or more interacting genes exert selective pressures on each other, leading to a linked evolutionary path. This can happen between genes in different species or within the same organism’s genome.
An example of coevolution is the “genetic arms race” between hosts and pathogens. A host’s immune system genes evolve to destroy a virus, which places pressure on the virus’s genes to change and evade detection. This drives further evolution in the host’s immune genes, creating a cycle of adaptation and counter-adaptation.
Coevolution also occurs within a single organism. For instance, a receptor protein and the ligand molecule that binds to it must evolve in a coordinated manner. A mutation changing the receptor’s shape requires a corresponding mutation in the ligand’s gene for the two to continue interacting. This intricate dance ensures that functionally linked genetic systems remain compatible as they evolve.