Everything about Epistasis totally explained
Epistasis is the
interaction between genes. Epistasis takes place when the action of one
gene is modified by one or several other genes, which are sometimes called
modifier genes. The gene whose
phenotype is expressed is said to be
epistatic, while the phenotype altered or suppressed is said to be
hypostatic.
In general, the fitness increment of any one allele depends in a complicated way on many other alleles; but, because of the way that the science of
population genetics was developed, evolutionary scientists tend to think of epistasis as the exception to the rule. In the first models of
natural selection devised in the early 20th century, each gene was considered to make its own characteristic contribution to fitness, against an average background of other genes. In introductory college courses,
population genetics is still taught this way.
Epistasis and
genetic interaction refer to the same phenomenon; however, epistasis is widely used in
population genetics and refers especially to the
statistical properties of the phenomenon.
Examples of tightly linked genes having epistatic effects on fitness are found in
supergenes and the human
major histocompatibility complex genes. The effect can occur directly at the genomic level, where one gene could code for a
protein preventing
transcription of the other gene. Alternatively, the effect can occur at the phenotypic level. For example, the gene causing
albinism would hide the gene controlling color of a person's hair. In another example, a gene coding for a
widow's peak would be hidden by a gene causing baldness.
Fitness epistasis (where the affected trait is fitness) is one cause of
linkage disequilibrium.
Studying genetic interactions can reveal gene function, the nature of the mutations, functional redundancy, and protein interactions. Because protein complexes are responsible for most biological functions, genetic interactions are a powerful tool.
Classification by fitness or trait value
Two-locus epistatic interactions can be either synergistic (negative) or antagonistic (positive). In the example of a
haploid organism with genotypes (at two
loci)
AB,
Ab,
aB and
ab, we can think of the following trait values where higher values suggest greater expression of the characteristic (the exact values are simply given as examples):
|
AB |
Ab |
aB |
ab |
| No epistasis (additive across loci) |
2 |
1 |
1 |
0 |
| Synergistic epistasis |
3 |
1 |
1 |
0 |
| Antagonistic epistasis |
1 |
1 |
1 |
0 |
Hence, we can classify thus:
| Trait values |
Type of epistasis |
| AB = Ab + aB - ab |
No epistasis, additive inheritance |
| AB > Ab + aB - ab |
Synergistic epistasis |
| AB < Ab + aB - ab |
Antagonistic epistasis |
Understanding whether the majority of genetic interactions are synergistic or antagonistic will help solve such problems as the
evolution of sex.
Epistasis and sex
Negative epistasis and sex are thought to be intimately correlated. Experimentally, this idea has been tested in using digital simulations of asexual and sexual populations. Over time, sexual populations move towards more negative epistasis, or the lowering of fitness by two interacting alleles. It is thought that negative epistasis allows individuals carrying the interacting deleterious mutations to be removed from the populations efficiently. This removes those alleles from the population, resulting in an overall more fit population. This hypothesis was proposed by
Alexey Kondrashov, and is sometimes known as the
deterministic mutation hypothesis
and has also been tested using artificial gene networks.
However, the evidence for this hypothesis hasn't always been straightforward and the model proposed by Kondrashov has often been criticized for assuming mutation parameters far from real world observations. For example, see
Functional or mechanistic classification
- Genetic suppression - the double mutant has a less severe phenotype than either single mutant.
- Genetic enhancement - the double mutant has a more severe phenotype than one predicted by the additive effects of the single mutants.
- Synthetic lethality or unlinked non-complementation - two mutations fail to complement and yet don't map to the same locus.
- Intragenic complementation, allelic complementation, or interallelic complementation - two mutations map to the same locus, yet the two alleles complement in the heteroallelic diploid. Causes of intragenic complementation include:
- homology effects such as transvection, where, for example, an enhancer from one allele acts in trans to activate transcription from the promoter of the second allele.
- trans-splicing of two mutant RNA molecules to produce a functional RNA.
- At the protein level, another possibility involves proteins that normally function as dimers. In a heteroallelic diploid, two different abnormal proteins could form a functional dimer if each can compensate for the lack of function in the other.
Further Information
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