The DOI matches its Crossref record; 35 of the 36 references it cites were found in a registry or an index.
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.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“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]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Mayr, E. (1963) · doi:10.4159/harvard.9780674865327 · Cited by 10,175
Adaptive protein evolution at the Adh locus in Drosophila
McDonald, J. H., & Kreitman, M. (1991) · Nature · doi:10.1038/351652a0 · Cited by 3,320
Hsp90 as a capacitor for morphological evolution
Rutherford, S. L., & Lindquist, S. (1998) · Nature · doi:10.1038/24550 · Cited by 2,270
The Probability of Duplicate Gene Preservation by Subfunctionalization
Lynch, M., & Force, A. G. (2000) · Genetics · doi:10.1093/genetics/154.1.459 · Cited by 1,559
Hsp90 as a capacitor of phenotypic variation
Queitsch, C., Sangster, T. A., & Lindquist, S. (2002) · Nature · doi:10.1038/nature749 · Cited by 1,372
The causes of molecular evolution
Gillespie, J. H. (1992) · Choice Reviews Online · doi:10.5860/choice.30-2064 · Cited by 1,214
The Nearly Neutral Theory of Molecular Evolution
Ohta, T. (1992) · Annual Review of Ecology and Systematics · doi:10.1146/annurev.es.23.110192.001403 · Cited by 1,149
Self-citationMechanisms of Speciation - A Population Genetic Approach
Templeton, A. R. (1981) · Annual Review of Ecology and Systematics · doi:10.1146/annurev.es.12.110181.000323 · Cited by 713
Akashi, H. D., & Gojobori, T. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.062526999 · Cited by 687
Adaptive protein evolution in Drosophila
Smith, N. G. C., & Eyre‐Walker, A. (2002) · Nature · doi:10.1038/4151022a · Cited by 677
Evidence for stabilizing selection in a eukaryotic enhancer element
Ludwig, M. Z., Bergman, C., Patel, N. H., & Kreitman, M. (2000) · Nature · doi:10.1038/35000615 · Cited by 574
Akashi, H. D. (1995) · Genetics · doi:10.1093/genetics/139.2.1067 · Cited by 559
Adaptive Evolution of Genes and Genomes
Zeyl, C., & Hughes, A. L. (2001) · Journal of Parasitology · doi:10.2307/3285093 · Cited by 502
How often do duplicated genes evolve new functions?
Walsh, J. B. (1995) · Genetics · doi:10.1093/genetics/139.1.421 · Cited by 418
The Evolution of Developmental Pathways
Wilkins, A. S. (2001) · Cited by 410
Testing the neutral theory of molecular evolution with genomic data from Drosophila
Fay, J. C., Wyckoff, G. J., & Wu, C. (2002) · Nature · doi:10.1038/4151024a · Cited by 357
(2001) · Elsevier eBooks · doi:10.1016/b978-0-12-205351-1.x5000-9 · Cited by 315
The cost of inbreeding in Arabidopsis
Bustamante, C. D., Nielsen, R., Sawyer, S. A., Olsen, K. M., Purugganan, M. D., & Hartl, D. L. (2002) · Nature · doi:10.1038/416531a · Cited by 311
THE SHIFTING BALANCE THEORY AND MACROEVOLUTION
Wright, S. (1982) · Annual Review of Genetics · doi:10.1146/annurev.ge.16.120182.000245 · Cited by 311
MOLECULAR EVIDENCE FOR NATURAL SELECTION
Kreitman, M., & Akashi, H. D. (1995) · Annual Review of Ecology and Systematics · doi:10.1146/annurev.es.26.110195.002155 · Cited by 280
Williams, J. A., Paddock, S. W., Vorwerk, K., & Carroll, S. B. (1994) · Nature · doi:10.1038/368299a0 · Cited by 255
Population size and rate of evolution
Ohta, T. (1972) · Journal of Molecular Evolution · doi:10.1007/bf01653959 · Cited by 197
Self-citationPopulation, Evolutionary and Genomic Consequences of Interference Selection
Comeron, J. M., & Kreitman, M. (2002) · Genetics · doi:10.1093/genetics/161.1.389 · Cited by 180
Invasion and maintenance of a gene duplication.
Clark, A. G. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.8.2950 · Cited by 152
Theoretical study of near neutrality. I. Heterozygosity and rate of mutant substitution.
Ohta, T., & Tachida, H. (1990) · Genetics · doi:10.1093/genetics/126.1.219 · Cited by 131
Self-citationSimulating Evolution by Gene Duplication
Ohta, T. (1987) · Genetics · doi:10.1093/genetics/115.1.207 · Cited by 121
Self-citationLauter, N., & Doebley, J. (2002) · Genetics · doi:10.1093/genetics/160.1.333 · Cited by 118
Weinreich, D. M., & Rand, D. M. (2000) · Genetics · doi:10.1093/genetics/156.1.385 · Cited by 115
Apparent changes in the diversity of fossil plants a preliminary assessment.
Kj, N., Tiffney, B. H., & Ah, K. (1980) · Journal of Evolutionary Biology · Cited by 78
A study on a nearly neutral mutation model in finite populations.
Tachida, H. (1991) · Genetics · doi:10.1093/genetics/128.1.183 · Cited by 66
Origin of new genes and source for N-terminal domain of the chimerical gene, jingwei, in Drosophila
Long, M., Wang, W., & Zhang, J. (1999) · Gene · doi:10.1016/s0378-1119(99)00229-2 · Cited by 61
FUNCTIONAL EFFECTS OF PGI ALLOZYMES IN ESCHERICHIA COLI
Dykhuizen, D. E., & Hartl, D. L. (1983) · Genetics · doi:10.1093/genetics/105.1.1 · Cited by 60
FURTHER SIMULATION STUDIES ON EVOLUTION BY GENE DUPLICATION
Ohta, T. (1988) · Evolution · doi:10.1111/j.1558-5646.1988.tb04140.x · Cited by 54
Self-citationRole of random genetic drift in the evolution of interactive systems
Ohta, T. (1997) · Journal of Molecular Evolution · doi:10.1007/pl00000054 · Cited by 25
Self-citationReductions in genetic variation inDrosophila andE. coli caused by selection at linked sites
Charlesworth, B., & Guttman, D. S. (1996) · Journal of Genetics · doi:10.1007/bf02931751 · Cited by 12
Research works printed but not linked: 3
- Carroll S. B. Grenier J. K. & Weatherbee S. D. (2001) From DNA to Diversity (Blackwell Scientific Oxford).
- 10.1046/j.1420-9101.1999.00008.x · DOI
- Ohta T. (2002) Genetica in press.
Cited by
Sorted by citations
Szabó, G., & Fáth, G. (2007) · Physics Reports · doi:10.1016/j.physrep.2007.04.004 · Cited by 2,965
“strategies are denoted by i and (N − i). This approach resembles the high temperature limit and seems to be adequate for biological systems where strategy changes have little effect on overall fitness (Ohta, 2002). The elementary steps can increase or decrease the value of i by 1 with probabilities µi+ and µi− given as…”
BackgroundGenome sequence, comparative analysis and haplotype structure of the domestic dog
members, B. S. P., Lindblad-Toh, K., Wade, C. M., Mikkelsen, T. S., Karlsson, E. K., Jaffe, D. B., Kamal, M., Clamp, M., Chang, J. L., Kulbokas, E. J., et al. (2005) · Nature · doi:10.1038/nature04338 · Cited by 2,568
“Population genetic theory predicts 75 that the strength of purifying selection should increase with effective population size ( N e ).”
BackgroundMolecular Signatures of Natural Selection
Nielsen, R. (2005) · Annual Review of Genetics · doi:10.1146/annurev.genet.39.073003.112420 · Cited by 1,698
Divergent selection and heterogeneous genomic divergence
Nosil, P., Funk, D. J., & Ortíz-Barrientos, D. (2009) · Molecular Ecology · doi:10.1111/j.1365-294x.2008.03946.x · Cited by 1,218
“…al. 2003; Haig 2004; Arnqvist & Rowe 2005; Crespi 2007; Presgraves 2007), the stochastic effects of genetic drift (Kimura 1968, 1986; King & Jukes 1969; Ohta 1992, 2002), variable mutation rates (Balloux & LugonMoulin 2002; Hedrick 2005; Noor & Feder 2006), the genomic distribution and effect size…”
BackgroundComputational Molecular Evolution
Yang, Z. (2006) · doi:10.1093/acprof:oso/9780198567028.001.0001 · Cited by 1,151
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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review