Clonal interference

Last updated
This diagram illustrates how sex might create novel genotypes more rapidly. Two advantageous alleles A and B occur at random. The two alleles are recombined rapidly in a sexual population (top), but in an asexual population (bottom) the two alleles often arise in separate lineages and compete with each other. Evolsex-dia2a.svg
This diagram illustrates how sex might create novel genotypes more rapidly. Two advantageous alleles A and B occur at random. The two alleles are recombined rapidly in a sexual population (top), but in an asexual population (bottom) the two alleles often arise in separate lineages and compete with each other.

Clonal interference is a phenomenon in evolutionary biology, related to the population genetics of organisms with significant linkage disequilibrium, especially asexually reproducing organisms. The idea of clonal interference was introduced by American geneticist Hermann Joseph Muller in 1932. [1] It explains why beneficial mutations can take a long time to get fixated or even disappear in asexually reproducing populations. As the name suggests, clonal interference occurs in an asexual lineage ("clone") with a beneficial mutation. This mutation would be likely to get fixed if it occurred alone, but it may fail to be fixed, or even be lost, if another beneficial-mutation lineage arises in the same population; the multiple clones interfere with each other.

Contents

Mechanism of clonal interference

Whenever a beneficial mutation arises in a population, for example mutation A, the carrier of the mutation obtains a higher fitness compared to members of the population without mutation A by means of natural selection. In the absence of genetic recombination (i.e. in asexually reproducing organisms) this beneficial mutation is only present in the clones of the cell in which the mutation arose. Because of this, the relative frequency of mutation A only increases slowly over time. In large asexually reproducing populations, it can take a long time before the mutation is fixated. In this time, another beneficial mutation, for example mutation B, can arise independently in another individual of the population. Mutation B also increases the fitness of the carrier. In this context, mutation A is often referred to as the ‘original mutation’, whereas mutation B is referred to as the ‘alternative’ or ‘interfering’ mutation. Since, due to the absence of genetic recombination, beneficial mutations A and B cannot (easily) be combined into a single genotype AB, carriers of mutation A and carriers of mutation B will compete against each other. This typically leads to the loss of one of them, [2] confirming that the fate of an advantageous mutation can be determined by other mutations present in the same population. [3]

On the contrary, in sexually reproducing populations, both carriers of mutations A and B have a higher fitness and therefore a higher chance to survive and to produce offspring. When a carrier of mutation A produces offspring with a carrier of mutation B, the ultimately more advantageous genotype AB can arise. Individuals with genotype AB are then no less likely to reproduce than at least one of: carriers of just the A mutation or carriers of just the B mutation ─ assuming that there is no negative interaction between the two. Thus, the relative frequency of both mutations A and B can increase rapidly, and both can be fixated simultaneously in the population. This allows evolution to proceed more rapidly, a phenomenon known as the Hill-Robertson effect.

Implications of clonal interference on adaptivity

When Muller introduced the phenomenon of clonal interference, he used it to explain why sexual reproduction evolved. He reasoned that the loss of beneficial mutations because of clonal interference inhibits the adaptivity of asexually reproducing species. Sex and other reproductive strategies involving recombination would therefore be evolutionary advantageous according to Muller. [1] From the 1970s, however, biologists have demonstrated that asexually and sexually reproducing strategies yield the same rate of the evolutionary adaptivity. This has to do with the fact that clonal interference also influences another part of the reproductive strategy of a population, namely mutation rate.

Clonal interference does not only play a role in the fixation of mutations in chromosomal DNA, but it also influences the stability or persistence of extrachromosomal DNA in the form of plasmids. [4] Plasmids often carry genes that code for traits like antibiotic resistance. Because of this, bacteria can become resistant to antibiotics in absence of genes coding for this trait in their chromosomal DNA. However, plasmids are not always adapted to their host cell, often resulting in the loss of the plasmid during cell division. Thus, the relative frequency of carriers of this plasmid in a population can decline. Nevertheless, the plasmids can also undergo mutations, resulting in competition between carriers of the plasmids. Because of this competition, the most stable plasmids will eventually get selected for and their frequency within the population will increase. This way, clonal interference influences the evolutionary dynamics of plasmid-host adaptation, resulting in faster stabilisation of plasmids in a population.

Clinical implications and applications

The phenomenon of clonal interference also occurs in cancer and pre-cancer cell lineages within a patient. [5] The heterogeneity found in cells of carcinogenic tumours implies competition between sub-populations of cells in the tumour, hence clonal interference. [6] Population dynamics within cancer lineages are therefore becoming of increasing importance in the clinical research on cancer treatments. [7] Furthermore, knowledge on the role of population dynamics and clonal interference, often resulting in antibiotic resistance, is being taken into account in the treatment of infectious diseases with antibiotics.

See also

Related Research Articles

<span class="mw-page-title-main">Mutation</span> Alteration in the nucleotide sequence of a genome

In biology, a mutation is an alteration in the nucleic acid sequence of the genome of an organism, virus, or extrachromosomal DNA. Viral genomes contain either DNA or RNA. Mutations result from errors during DNA or viral replication, mitosis, or meiosis or other types of damage to DNA, which then may undergo error-prone repair, cause an error during other forms of repair, or cause an error during replication. Mutations may also result from insertion or deletion of segments of DNA due to mobile genetic elements.

Fitness is a quantitative representation of individual reproductive success. It is also equal to the average contribution to the gene pool of the next generation, made by the same individuals of the specified genotype or phenotype. Fitness can be defined either with respect to a genotype or to a phenotype in a given environment or time. The fitness of a genotype is manifested through its phenotype, which is also affected by the developmental environment. The fitness of a given phenotype can also be different in different selective environments.

Population genetics is a subfield of genetics that deals with genetic differences within and among populations, and is a part of evolutionary biology. Studies in this branch of biology examine such phenomena as adaptation, speciation, and population structure.

<span class="mw-page-title-main">Muller's ratchet</span> Accumulation of harmful mutations

In evolutionary genetics, Muller's ratchet is a process which, in the absence of recombination, results in an accumulation of irreversible deleterious mutations. This happens because in the absence of recombination, and assuming reverse mutations are rare, offspring bear at least as much mutational load as their parents. Muller proposed this mechanism as one reason why sexual reproduction may be favored over asexual reproduction, as sexual organisms benefit from recombination and consequent elimination of deleterious mutations. The negative effect of accumulating irreversible deleterious mutations may not be prevalent in organisms which, while they reproduce asexually, also undergo other forms of recombination. This effect has also been observed in those regions of the genomes of sexual organisms that do not undergo recombination.

In evolutionary genetics, mutational meltdown is a sub class of extinction vortex in which the environment and genetic predisposition mutually reinforce each other. Mutational meltdown is the accumulation of harmful mutations in a small population, which leads to loss of fitness and decline of the population size, which may lead to further accumulation of deleterious mutations due to fixation by genetic drift.

<span class="mw-page-title-main">Evolution of sexual reproduction</span> How sexually reproducing multicellular organisms could have evolved from a common ancestor species

Sexual reproduction is an adaptive feature which is common to almost all multicellular organisms and various unicellular organisms. Currently, the adaptive advantage of sexual reproduction is widely regarded as a major unsolved problem in biology. As discussed below, one prominent theory is that sex evolved as an efficient mechanism for producing variation, and this had the advantage of enabling organisms to adapt to changing environments. Another prominent theory, also discussed below, is that a primary advantage of outcrossing sex is the masking of the expression of deleterious mutations. Additional theories concerning the adaptive advantage of sex are also discussed below. Sex does, however, come with a cost. In reproducing asexually, no time nor energy needs to be expended in choosing a mate and, if the environment has not changed, then there may be little reason for variation, as the organism may already be well-adapted. However, very few environments have not changed over the millions of years that reproduction has existed. Hence it is easy to imagine that being able to adapt to changing environment imparts a benefit. Sex also halves the amount of offspring a given population is able to produce. Sex, however, has evolved as the most prolific means of species branching into the tree of life. Diversification into the phylogenetic tree happens much more rapidly via sexual reproduction than it does by way of asexual reproduction.

Evolvability is defined as the capacity of a system for adaptive evolution. Evolvability is the ability of a population of organisms to not merely generate genetic diversity, but to generate adaptive genetic diversity, and thereby evolve through natural selection.

Genetic load is the difference between the fitness of an average genotype in a population and the fitness of some reference genotype, which may be either the best present in a population, or may be the theoretically optimal genotype. The average individual taken from a population with a low genetic load will generally, when grown in the same conditions, have more surviving offspring than the average individual from a population with a high genetic load. Genetic load can also be seen as reduced fitness at the population level compared to what the population would have if all individuals had the reference high-fitness genotype. High genetic load may put a population in danger of extinction.

<span class="mw-page-title-main">Loss of heterozygosity</span>

Loss of heterozygosity (LOH) is a type of genetic abnormality in diploid organisms in which one copy of an entire gene and its surrounding chromosomal region are lost. Since diploid cells have two copies of their genes, one from each parent, a single copy of the lost gene still remains when this happens, but any heterozygosity is no longer present.

<span class="mw-page-title-main">Thelytoky</span> Type of parthenogenesis in which females are produced from unfertilized eggs

Thelytoky is a type of parthenogenesis and is the absence of mating and subsequent production of all female diploid offspring as for example in aphids. Thelytokous parthenogenesis is rare among animals and reported in about 1,500 species, about 1 in 1000 of described animal species, according to a 1984 study. It is more common in invertebrates, like arthropods, but it can occur in vertebrates, including salamanders, fish, and reptiles such as some whiptail lizards.

In population genetics, the Hill–Robertson effect, or Hill–Robertson interference, is a phenomenon first identified by Bill Hill and Alan Robertson in 1966. It provides an explanation as to why there may be an evolutionary advantage to genetic recombination.

The Red Queen's hypothesis is a hypothesis in evolutionary biology proposed in 1973, that species must constantly adapt, evolve, and proliferate in order to survive while pitted against ever-evolving opposing species. The hypothesis was intended to explain the constant (age-independent) extinction probability as observed in the paleontological record caused by co-evolution between competing species; however, it has also been suggested that the Red Queen hypothesis explains the advantage of sexual reproduction at the level of individuals, and the positive correlation between speciation and extinction rates in most higher taxa.

<i>E. coli</i> long-term evolution experiment Scientific study

The E. coli long-term evolution experiment (LTEE) is an ongoing study in experimental evolution begun by Richard Lenski at the University of California, Irvine, carried on by Lenski and colleagues at Michigan State University, and currently overseen by Jeffrey E. Barrick at the University of Texas at Austin. It has been tracking genetic changes in 12 initially identical populations of asexual Escherichia coli bacteria since 24 February 1988. Lenski performed the 10,000th transfer of the experiment on March 13, 2017. The populations reached over 73,000 generations in early 2020, shortly before being frozen because of the COVID-19 pandemic. In September 2020, the LTEE experiment was resumed using the frozen stocks.

<span class="mw-page-title-main">Vicar of Bray (scientific hypothesis)</span> Fisherian explanation of the evolution of sexual reproduction and recombination

The "Vicar of Bray" hypothesis attempts to explain why sexual reproduction might have advantages over asexual reproduction. Reproduction is the process by which organisms give rise to offspring. Asexual reproduction involves a single parent and results in offspring that are genetically identical to each other and to the parent.

Host–parasite coevolution is a special case of coevolution, where a host and a parasite continually adapt to each other. This can create an evolutionary arms race between them. A more benign possibility is of an evolutionary trade-off between transmission and virulence in the parasite, as if it kills its host too quickly, the parasite will not be able to reproduce either. Another theory, the Red Queen hypothesis, proposes that since both host and parasite have to keep on evolving to keep up with each other, and since sexual reproduction continually creates new combinations of genes, parasitism favours sexual reproduction in the host.

Tumour heterogeneity describes the observation that different tumour cells can show distinct morphological and phenotypic profiles, including cellular morphology, gene expression, metabolism, motility, proliferation, and metastatic potential. This phenomenon occurs both between tumours and within tumours. A minimal level of intra-tumour heterogeneity is a simple consequence of the imperfection of DNA replication: whenever a cell divides, a few mutations are acquired—leading to a diverse population of cancer cells. The heterogeneity of cancer cells introduces significant challenges in designing effective treatment strategies. However, research into understanding and characterizing heterogeneity can allow for a better understanding of the causes and progression of disease. In turn, this has the potential to guide the creation of more refined treatment strategies that incorporate knowledge of heterogeneity to yield higher efficacy.

<span class="mw-page-title-main">Epistasis</span> Dependence of a gene mutations phenotype on mutations in other genes

Epistasis is a phenomenon in genetics in which the effect of a gene mutation is dependent on the presence or absence of mutations in one or more other genes, respectively termed modifier genes. In other words, the effect of the mutation is dependent on the genetic background in which it appears. Epistatic mutations therefore have different effects on their own than when they occur together. Originally, the term epistasis specifically meant that the effect of a gene variant is masked by that of different gene.

This glossary of genetics and evolutionary biology is a list of definitions of terms and concepts used in the study of genetics and evolutionary biology, as well as sub-disciplines and related fields, with an emphasis on classical genetics, quantitative genetics, population biology, phylogenetics, speciation, and systematics. Overlapping and related terms can be found in Glossary of cellular and molecular biology, Glossary of ecology, and Glossary of biology.

PyClone is a software that implements a Hierarchical Bayes statistical model to estimate cellular frequency patterns of mutations in a population of cancer cells using observed alternate allele frequencies, copy number, and loss of heterozygosity (LOH) information. PyClone outputs clusters of variants based on calculated cellular frequencies of mutations.

Daniel S. Fisher is an American theoretical physicist working in statistical physics.

References

  1. 1 2 Gerrish PJ, Lenski RE (1998), "The fate of competing beneficial mutations in an asexual population", Mutation and Evolution, vol. 102–103, no. 1–6, Springer Netherlands, pp. 127–144, doi:10.1007/978-94-011-5210-5_12, ISBN   9789401061933, PMID   9720276
  2. Imhof M, Schlotterer C (January 2001). "Fitness effects of advantageous mutations in evolving Escherichia coli populations". Proceedings of the National Academy of Sciences of the United States of America. 98 (3): 1113–7. doi: 10.1073/pnas.98.3.1113 . PMC   14717 . PMID   11158603.
  3. Lang GI, Rice DP, Hickman MJ, Sodergren E, Weinstock GM, Botstein D, Desai MM (August 2013). "Pervasive genetic hitchhiking and clonal interference in forty evolving yeast populations". Nature. 500 (7464): 571–4. doi:10.1038/nature12344. PMC   3758440 . PMID   23873039.
  4. Hughes JM, Lohman BK, Deckert GE, Nichols EP, Settles M, Abdo Z, Top EM (2012-08-31). "The role of clonal interference in the evolutionary dynamics of plasmid-host adaptation". mBio. 3 (4): e00077–12. doi:10.1128/mBio.00077-12. PMC   3398533 . PMID   22761390.
  5. Baker AM, Graham TA, Wright NA (March 2013). "Pre-tumour clones, periodic selection and clonal interference in the origin and progression of gastrointestinal cancer: potential for biomarker development". The Journal of Pathology. 229 (4): 502–14. doi:10.1002/path.4157. PMID   23288692. S2CID   43031735.
  6. Marusyk A, Tabassum DP, Altrock PM, Almendro V, Michor F, Polyak K (October 2014). "Non-cell-autonomous driving of tumour growth supports sub-clonal heterogeneity". Nature. 514 (7520): 54–8. doi:10.1038/nature13556. PMC   4184961 . PMID   25079331.
  7. Korolev KS, Xavier JB, Gore J (May 2014). "Turning ecology and evolution against cancer". Nature Reviews. Cancer. 14 (5): 371–80. doi:10.1038/nrc3712. PMID   24739582. S2CID   10596049.