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Convergent acquisition of disulfide-forming enzymes in malodorous flowers
Abstract
Identifying the metabolic and genetic changes that confer evolutionary novelty is essential for understanding the factors facilitating or constraining the occurrence of traits. We show that dimethyl disulfide (DMDS), a volatile compound that attracts saprophilous pollinators, is produced by a disulfide synthase (DSS) in the plant genus Asarum (Aristolochiaceae). DSS is derived from methanethiol oxidase (MTOX), an enzyme conserved among animals and plants, and similar DSS enzymes have independently evolved in two other plant genera. Three amino acid changes shared among the DSSs of independent origins were sufficient to cause a functional switch between MTOX and DSS. The small number of amino acid changes and the co-option of a highly conserved enzyme may explain why DMDS-emitting flowers are widespread among floral mimics.
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For simple traits with easily quantifiable phenotypes and a simple genetic basis, PhyloG2P studies will have a chance to identify specific genotype-to-phenotype maps.
“On one end, we can conceptualize “simple” traits with both easily quantifiable phenotypes and a simple genetic basis. Here PhyloG2P studies will have a chance to identify specific genotype to phenotype maps (Lamichhaney et al. 2019; Nagy et al. 2020; Okuyama et al. 2025).”
From From Trees to Traits: A Review of Advances in PhyloG2P Methods and Future Directions (2025) · cites this paper as Okuyama et al. 2025
After identifying the responsible gene, Okuyama et al. used CSUBST to identify replicated amino acid substitutions in the foreground lineages.
“After identifying the responsible gene, they used CSUBST (Fukushima and Pollock 2023) to identify replicated amino acid substitutions in the foreground lineages.”
From From Trees to Traits: A Review of Advances in PhyloG2P Methods and Future Directions (2025) · cites this paper as Okuyama et al. 2025
Okuyama et al.'s study highlights how PhyloG2P methods can complement other molecular genetics methods.
“This study highlights how PhyloG2P methods can compliment other molecular genetics methods.”
From From Trees to Traits: A Review of Advances in PhyloG2P Methods and Future Directions (2025) · cites this paper as Okuyama et al. 2025
Okuyama et al.'s analysis identified three substitutions within the gene that had occurred in all three independent transitions studied.
“Their analysis identified three substitutions within the gene that had occurred in all three independent transitions studied.”
From From Trees to Traits: A Review of Advances in PhyloG2P Methods and Future Directions (2025) · cites this paper as Okuyama et al. 2025
Okuyama et al.'s follow-up experiments manipulating those three sites confirmed they were necessary and sufficient to cause the phenotypic change.
“Their follow up experiments manipulating those three sites confirmed they were necessary and sufficient to cause the phenotypic change.”
From From Trees to Traits: A Review of Advances in PhyloG2P Methods and Future Directions (2025) · cites this paper as Okuyama et al. 2025
Okuyama et al. chose CSUBST because the gene was highly conserved between species and they wanted to identify any identical substitutions driving the replicated phenotypic change.
“Okuyama et al. (2025) chose CSUBST because the gene was highly conserved between species and they wanted to identify any identical substitutions driving the replicated phenotypic change.”
From From Trees to Traits: A Review of Advances in PhyloG2P Methods and Future Directions (2025) · cites this paper as Okuyama et al. 2025
Okuyama et al. (2025) used a range of transcriptomic, molecular, and transgenic approaches to understand the genetic mechanisms underlying replicated changes in floral scent compounds.
“Okuyama et al. (2025) used a range of transcriptomic, molecular, and transgenic approaches to understand the genetic mechanisms underlying replicated changes in floral scent compounds.”
From From Trees to Traits: A Review of Advances in PhyloG2P Methods and Future Directions (2025) · cites this paper as Okuyama et al. 2025
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Fukushima, K., & Pollock, D. D. (2023) · Nature Ecology & Evolution · doi:10.1038/s41559-022-01932-7 · Cited by 55
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From Trees to Traits: A Review of Advances in PhyloG2P Methods and Future Directions
Macdonald, A. R., James, M. E., Mitchell, J. D., & Holland, B. R. (2025) · Genome Biology and Evolution · doi:10.1093/gbe/evaf150 · Cited by 5
Metadata
- Authors
- Okuyama, Y., Fukushima, K., Kakishima, S., Valchanova, A. K., Takano, K. T., Ito-Inaba, Y., Nakazato, T., & Nagano, A. J.
- Affiliations
- Tsukuba Botanical Garden, Department of Botany, National Museum of Nature and Science, Tsukuba, Japan.
- National Institute of Genetics, Mishima, Japan.
- The Mt. Fuji Institute for Nature and Biology, Showa Medical University, Fuji-Yoshida, Japan.
- Graduate School of Science, The University of Tokyo, Tokyo, Japan.
- Nagano Environmental Conservation Research Institute, Nagano, Japan.
- Faculty of Agriculture, University of Miyazaki, Miyazaki, Japan.
- Database Center for Life Science, Research Organization of Information and Systems, Chiba, Japan.
- Faculty of Agriculture, Ryukoku University, Otsu, Japan.
- ORCID
- Venue
- Science
- Published
- 2025-05-08
- Volume
- 388
- Issue
- 6747
- Pages
- 656-661
- ISSN
- 0036-8075
- 1095-9203
- Cited by
- 17
- References
- 4
- Language
- en
- Update notices
- correction (2026-01-01)
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