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Near-neutrality in evolution of genes and gene regulation
Open accessAbstract
The nearly neutral theory contends that the interaction of drift and selection is important and occurs at various levels, including synonymous and nonsynonymous substitutions in protein coding regions and sequence turnover of regulatory elements. Recent progress of the theory is reviewed, and the interaction between drift and selection is suggested to differ at these different levels. Weak selective force on synonymous changes is stable, whereas its consequence on nonsynonymous changes depends on environmental factors. Selection on differentiation of regulatory elements is even more dependent on environmental factors than on amino acid changes. Of particular significance is the role of drift in the evolution of gene regulation that directly participates in morphological evolution. The range of near neutrality depends on the effective size of the population that is influenced by selected linked loci. In addition to the effective population size, molecular chaperones such as heat shock protein 90 have significant effects on the range of near neutrality.
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“Therefore, the fixation of nearly-neutral alleles of small selective effect is expected to be greatest in small populations 23,24 .”
From The modern molecular clock (2003) · cites this paper as [24]
In the citing paper
“The predicted correlation of generation time with mutation rate 24 has been supported by studies that compare the rates of molecular evolution with generation time (or its correlate, body size) across a range of genes for several vertebrate species 35,37-39 .”
From The modern molecular clock (2003) · cites this paper as [24]
In the citing paper
“Tomoko Ohta 22-24 provided an important extension of the neutral theory by recognizing the crucial role of effective population size in the influence of selection.”
From The modern molecular clock (2003) · cites this paper as [24]
In the citing paper
“So, a mutation would be effectively neutral if |s| < 1/4N e , where N e is the effective population size.”
From The modern molecular clock (2003) · cites this paper as [24]
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“-regulatory alleles are expected to be present at appreciable frequencies, and an interplay of forces, including changes in effective population size, linkage disequilibrium among selected alleles, and epistatic selection”
Kaneko‐Ishino, T., & Ishino, F. (2010) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2010.01194.x · Cited by 52
“According to the ‘‘nearly neutral theory’’ by Tomoko Ohta (2002), an extended version of ‘‘the neutral mutation-random drift theory’’ proposed by Motoo Kimura (1968), neutral or even ‘‘less harmful’’ genes can become established in a population to some extent if the population size is small enough.”
BackgroundBaquero, F. (2011) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkr214 · Cited by 50
Hughes, A. L., & Friedman, R. (2008) · Immunogenetics · doi:10.1007/s00251-008-0304-4 · Cited by 49
“If this slightly deleterious mutation becomes fixed during a population bottleneck (Ohta 2002), a subsequent mutation may occur that reintroduces serine at that site but that uses a different codon set from the one used ancestrally.”
BackgroundAn overview of speciation and species limits in birds
Winker, K. (2021) · The Auk · doi:10.1093/ornithology/ukab006 · Cited by 47
“…datasets have gone from purely phenotypic—and thus rich in the signals of natural, sexual, and social selection—to include increasing amounts of genomic information, in which the signal is overwhelmingly neutral or nearly neutral through the effects of mutation and drift (Kimura 1983, Ohta 2002).”
BackgroundLarge Global Effective Population Sizes in Paramecium
Smith, M. S., Berendonk, T. U., Barth, D., & Lynch, M. (2006) · Molecular Biology and Evolution · doi:10.1093/molbev/msl128 · Cited by 46
“Because the probabilities of fixation of beneficial and deleterious mutations, respectively, scale positively and negatively with Ne, species with smaller Ne are expected to accumulate more mildly deleterious and fewer beneficial mutations (Ohta 1973, 2002).”
BackgroundChalub, F. A. C. C., & Souza, M. O. (2009) · Theoretical Population Biology · doi:10.1016/j.tpb.2009.08.006 · Cited by 44
Evolution and Taxonomic Distribution of Nonribosomal Peptide and Polyketide Synthases
Amoutzias, G. D., de Peer, Y. V., & Mossialos, D. (2008) · Future Microbiology · doi:10.2217/17460913.3.3.361 · Cited by 44
“Given the strong link between effective population size and the efficiency of selection in a certain species, which the nearly neutral theory of molecular evolution suggests [29], it is expected that microorganisms will jettison unnecessary gene clusters very rapidly.”
BackgroundHuman SNPs resulting in premature stop codons and protein truncation
Savas, S., Tüzmen, Ş., & Özçelik, H. (2006) · Human Genomics · doi:10.1186/1479-7364-2-5-274 · Cited by 44
“Here, we will assume that these PTCs represent both the strongly deleterious mutations that are a result of selection and quickly removed from the populations, as well as the slightly deleterious mutations that are subject to both selection and drift.(36) For example, these X-SNPs may be hot-spot mutations, where the…”
BackgroundAkashi, H. D., Ko, W., Piao, S., John, A., Goel, P., Lin, C., & Vitins, A. P. (2005) · Genetics · doi:10.1534/genetics.105.049676 · Cited by 44
“A great deal of attention has been focused on determining the relative contributions of genetic drift and natural selection to patterns of divergence among genomes (reviewed in Ohta 2002).”
BackgroundSelection efficiency and effective population size in Drosophila species
Petit, N., & Barbadilla, A. (2008) · Journal of Evolutionary Biology · doi:10.1111/j.1420-9101.2008.01672.x · Cited by 44
“In this nearly neutral theory, the fate of a mutation depends on the relative forces of selection and drift (Ohta, 2002).”
BackgroundStochastic slowdown in evolutionary processes
Altrock, P. M., Gokhale, C. S., & Traulsen, A. (2010) · Physical Review E · doi:10.1103/physreve.82.011925 · Cited by 41
Santos, U., Völcker, C. M., Belei, F., Cioffi, M. D. B., Bertollo, L. A. C., Paiva, S. R., & Dergam, J. A. (2009) · Journal of Fish Biology · doi:10.1111/j.1095-8649.2009.02489.x · Cited by 40
“Slightly disadvantageous substitutions can drift to high frequencies in small populations (Ohta, 2002), thereby altering substitution rates in the DNA.”
BackgroundXu, S., Yang, Y., Zhou, X., Xu, J., Zhou, K., & Yang, G. (2013) · BMC Evolutionary Biology · doi:10.1186/1471-2148-13-189 · Cited by 39
“Population genetic theory predicts that the efficiency of selection should decrease as the effective population size decreses [48].”
BackgroundPerpendicular axes of differentiation generated by mitochondrial introgression
Morales, H. E., Sunnucks, P., Joseph, L., & Pavlova, A. (2017) · Molecular Ecology · doi:10.1111/mec.14114 · Cited by 40
“We propose that first, large ancestral northern and southern population sizes could have promoted the accumulation of adaptive mitochondrial variation in each lineage (Fig. 3A; Kimura et al. 1963; Ohta 2002; Camus et al. 2015).”
BackgroundCoding sequence polymorphism in avian mitochondrial genomes reflects population histories
Hughes, A. L., & Hughes, M. A. K. (2007) · Molecular Ecology · doi:10.1111/j.1365-294x.2007.03242.x · Cited by 39
“Under a population bottleneck, the ‘nearly neutral theory’ predicts that slightly deleterious mutations can drift to high frequencies because purifying selection cannot eliminate them effectively in a small population ( Ohta 1976, 2002 ).”
BackgroundInfluentialDetecting and understanding natural selection
Anisimova, M. O., & Liberles, D. A. (2012) · Oxford University Press eBooks · doi:10.1093/acprof:osobl/9780199601165.003.0006 · Cited by 39
Zhao, Q., Shao, F., Li, Y.-P., Yi, S. V., & Peng, Z.-G. (2022) · Molecular Ecology · doi:10.1111/mec.16700 · Cited by 32
“…elements, which can provide material for the evolution of novel regulatory mechanisms and complexities in the genome (e.g., Lynch, 2007; Lynch & Conery, 2003; Ohta, 2002; Yi, 2006; Yi & Streelman, 2005, although see Whitney et al., 2011 and Whitney & Garland, 2010 for differing observations).”
BackgroundKaneko‐Ishino, T., & Ishino, F. (2015) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.91.511 · Cited by 38
Molecular Clock: An Anti-neo-Darwinian Legacy
Takahata, N. (2007) · Genetics · doi:10.1534/genetics.104.75135 · Cited by 38
“Another mechanistic interpretation for the rate heterogeneity was provided by fixation of nearly neutral, but slightly deleterious, mutations (Ohta 1987, 2002).”
BackgroundPyoverdine Receptor: a Case of Positive Darwinian Selection inPseudomonas aeruginosa
Tümmler, B., & Cornélis, P. (2005) · Journal of Bacteriology · doi:10.1128/jb.187.10.3289-3292.2005 · Cited by 38
“Being not just another sequence paper, it provides food for thought how positive selection and adaptive evolution may work in species with very large population sizes, which is the domain of the nearly neutral theory of molecular evolution (20, 27).”
BackgroundLarge fluctuations and fixation in evolutionary games
Assaf, M., & Mobilia, M. (2010) · Journal of Statistical Mechanics Theory and Experiment · doi:10.1088/1742-5468/2010/09/p09009 · Cited by 37
Pellissier, L. (2015) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2015.00052 · Cited by 35
“Together, ecological and evolutionary demographic theories suggest a direct connection between stability, competition, lower dispersal, and decreased effective population size (Figure 1).”
BackgroundKalamegham, R., Sturgill, D. M., Siegfried, E., & Oliver, B. (2006) · Molecular Biology and Evolution · doi:10.1093/molbev/msl201 · Cited by 34
Technical trading in the Santa Fe Institute Artificial Stock Market revisited
Ehrentreich, N. (2006) · Journal of Economic Behavior & Organization · doi:10.1016/j.jebo.2004.07.022 · Cited by 34
Molecular Adaptation during a Rapid Adaptive Radiation
Kapralov, M. V., Votintseva, A. A., & Filatov, D. A. (2013) · Molecular Biology and Evolution · doi:10.1093/molbev/mst013 · Cited by 34
“The small population sizes of island species may render selection less effective in the face of stronger genetic drift (Ohta 2002) and the genetic processes that control the rapid morphological and ecological evolution during island adaptive radiations remain unclear.”
Background
Metadata
- Authors
- Ohta, T.
- Affiliations
- National Institute of Genetics (JP)
- Corresponding author
- Ohta, Tomoko
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2002-12-02
- Volume
- 99
- Issue
- 25
- Pages
- 16134-16137
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC138577
- OpenAlex
- W1963674435
- Cited by
- 333
- References
- 36
- Citations by year
- 2026: 7 · 2025: 5 · 2024: 1 · 2023: 8 · 2022: 8 · 2021: 12 · 2020: 6 · 2019: 19 · 2018: 7 · 2017: 15 · 2016: 9 · 2015: 9 · 2014: 23 · 2013: 25 · 2012: 10
- FWCI
- 6.01
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Social Sciences › Arts and Humanities › History and Philosophy of Science › Philosophy of Biology and Scientific Explanation
- Keywords
- nearly neutral theory, genetic drift, natural selection, synonymous substitutions, nonsynonymous substitutions, gene regulatory evolution, morphological evolution, effective population size, linked loci, HSP90, molecular chaperones
- MeSH terms
- Animals, Drosophila, Drosophila melanogaster, Gene Expression Regulation, Genes, Genetic Linkage, Models, Genetic, Regulatory Sequences, Nucleic Acid, Selection, Genetic, Species Specificity, Arabidopsis, Molecular Chaperones, Evolution, Molecular, Amino Acid Substitution, Genetic Drift
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