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Fractionation mutagenesis and similar consequences of mechanisms removing dispensable or less-expressed DNA in plants
Abstract
Unlike in mammals, plants rapidly delete functionless, nonrepetitive DNA from their genomes. Following paleopolyploidies, duplicate genes are deleted by intrachromosomal recombination. This may explain how flowering plants have survived multiple whole genome duplications. Genes are disproportionately lost from one parental subgenome, the subgenome that is less expressed in the polyploid. The origin of this unbalanced expression between genomes remains unknown. The consequences of the tradeoffs between transposon repression and gene expression represent one potential explanation of genome dominance. If so, the same mechanisms may act in heterosis: genome dominance is like inbreeding depression. Regulatory DNA deletion following polyploidy combined with abundant RNA-seq expression datasets are being used to generate testable hypothesizes regarding the function of specific cis-regulatory sequences.
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Genes on silenced chromosome copies are expressed at lower levels, and therefore subjected to lower selective pressures and ultimately to pseudogenization.
“Genes on silenced chromosome copies are expressed at lower levels, and therefore subjected to lower selective pressures and ultimately to pseudogenization.”
From An atlas of fish genome evolution reveals delayed rediploidization following the teleost whole-genome duplication (2022) · cites this paper as Freeling et al. 2012
Previous observations have suggested that biased gene retention in allopolyploid genomes reflects partial epigenetic silencing of one parental subgenome.
“Previous observations have suggested that biased gene retention in allopolyploid genomes reflects partial epigenetic silencing of one parental subgenome (Freeling et al. 2012; Bird et al. 2021).”
From An atlas of fish genome evolution reveals delayed rediploidization following the teleost whole-genome duplication (2022) · cites this paper as Freeling et al. 2012
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Mapping copy number variation by population-scale genome sequencing
1000 Genomes Project, Mills, R. E., Walter, K., Stewart, C., Handsaker, R. E., Chen, K., Alkan, C., Abyzov, A., Yoon, S. C., Ye, K., et al. (2011) · Nature · doi:10.1038/nature09708 · Cited by 1,140
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McLean, C. Y., Reno, P. L., Pollen, A. A., Bassan, A. I., Capellini, T. D., Guenther, C., Indjeian, V. B., Lim, X., Menke, D. B., Schaar, B. T., et al. (2011) · Nature · doi:10.1038/nature09774 · Cited by 535
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Cited by
Sorted by citations
Parey, E., Louis, A., Montfort, J., Guiguen, Y., Crollius, H. R., & Berthelot, C. (2022) · Genome Research · doi:10.1101/gr.276953.122 · Cited by 83
Metadata
- Authors
- Freeling, M., Woodhouse, M. R., Subramaniam, S., Turco, G., Lisch, D., & Schnable, J. C.
- Venue
- Current Opinion in Plant Biology
- Publisher
- Elsevier BV
- Published
- 2012-04
- Volume
- 15
- Issue
- 2
- Pages
- 131-139
- ISSN
- 1369-5266
- Cited by
- 198
- References
- 3
- Language
- en
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