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Role of selection in fixation of gene duplications
Abstract
New genes commonly appear through complete or partial duplications of pre-existing genes. Duplications of long DNA segments are constantly produced by rare mutations, may become fixed in a population by selection or random drift, and are subject to divergent evolution of the paralogous sequences after fixation, although gene conversion can impede this process. New data shed some light on each of these processes. Mutations which involve duplications can occur through at least two different mechanisms, backward strand slippage during DNA replication and unequal crossing-over. The background rate of duplication of a complete gene in humans is 10(-9)-10(-10) per generation, although many genes located within hot-spots of large-scale mutation are duplicated much more often. Many gene duplications affect fitness strongly, and are responsible, through gene dosage effects, for a number of genetic diseases. However, high levels of intrapopulation polymorphism caused by presence or absence of long, gene-containing DNA segments imply that some duplications are not under strong selection. The polymorphism to fixation ratios appear to be approximately the same for gene duplications and for presumably selectively neutral nucleotide substitutions, which, according to the McDonald-Kreitman test, is consistent with selective neutrality of duplications. However, this pattern can also be due to negative selection against most of segregating duplications and positive selection for at least some duplications which become fixed. Patterns in post-fixation evolution of duplicated genes do not easily reveal the causes of fixations. Many gene duplications which became fixed recently in a variety of organisms were positively selected because the increased expression of the corresponding genes was beneficial. The effects of gene dosage provide a unified framework for studying all phases of the life history of a gene duplication. Application of well-known methods of evolutionary genetics to accumulating data on new, polymorphic, and fixed duplication will enhance our understanding of the role of natural selection in the evolution by gene duplication.
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“Examples for adaptive cross-protection are also available for S. cerevisiae where cobalt resistance also improved tolerance for other metal ions and pulsed cobalt stress exposure during laboratory evolution even resulted in evolutionary cross-protection to thermal and oxidative stress [114].”
From Adaptive laboratory evolution—Principles and applications for biotechnology (2013) · cites this paper as [114]
In the citing paper
“Other studies used ethylmethanesulfonate (EMS) treated Bacillus boroniphilus to select for increased boron resistance [88] or EMS-treated S. cerevisiae in order to achieve increased nutrient utilization and stress resistance [95,113,114].”
From Adaptive laboratory evolution—Principles and applications for biotechnology (2013) · cites this paper as [114]
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Cited by
Sorted by citations
The evolution of gene duplications: classifying and distinguishing between models
Innan, H., & Kondrashov, F. A. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2689 · Cited by 1,338
“However, as data from eukaryotes became more widely available, authors started to relate dosage and gene duplications in multicellular organism”
BackgroundSelf-citationTurning a hobby into a job: How duplicated genes find new functions
Conant, G. C., & Wolfe, K. H. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2482 · Cited by 1,281
“Duplicate gene pairs can also be preserved by selection for increased gene dosag”
BackgroundAdaptive laboratory evolution—Principles and applications for biotechnology
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“Whereas there is an ongoing debate about the long-term fixation of gene duplications, either by their selective advantage under selection pressure, or by selective neutrality and fixation by random drift, they are a prerequisite for the development of novel molecular functions [129-131].”
BackgroundGene duplication as a mechanism of genomic adaptation to a changing environment
Kondrashov, F. A. (2012) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2012.1108 · Cited by 663
Self-citationDistinguishing Among Evolutionary Models for the Maintenance of Gene Duplicates
Hahn, M. W. (2009) · Journal of Heredity · doi:10.1093/jhered/esp047 · Cited by 428
“Multiple authors have also recently proposed that this is a major force in duplicate gene retention (Kondrashov et al. 2002; Kondrashov and Kondrashov 2006; Sugino and Innan 2006).”
Background
Metadata
- Authors
- Kondrashov, F. A., & Kondrashov, A. S.
- Affiliations
- National Center for Biotechnology Information (US)
- Corresponding author
- Kondrashov, Fyodor A.
- Kondrashov, Alexey S.
- Venue
- Journal of Theoretical Biology
- Publisher
- Elsevier BV
- Published
- 2006-03
- Volume
- 239
- Issue
- 2
- Pages
- 141-151
- ISSN
- 0022-5193 (ISSN-L)
- OpenAlex
- W2018486257
- Cited by
- 195
- References
- 150
- Citations by year
- 2026: 3 · 2025: 8 · 2024: 3 · 2023: 6 · 2022: 9 · 2021: 4 · 2020: 6 · 2019: 7 · 2018: 10 · 2017: 12 · 2016: 6 · 2015: 11 · 2014: 11 · 2013: 10 · 2012: 13
- FWCI
- 1.01
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Theoretical Biology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genome Rearrangement Algorithms
- Keywords
- gene duplication, natural selection, paralogs, gene conversion, unequal crossover, replication slippage, McDonald-Kreitman test, gene dosage effect, positive selection
- MeSH terms
- Animals, Humans, Mutation, Selection, Genetic, Genome, Gene Dosage, Evolution, Molecular, Gene Duplication
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