ArticleCurrent biology : CB2025
Distinct haplotypes and reversed dominance at a single-gene balanced polymorphism controlling heterodichogamy in two genera of wingnuts.
Article in Current biology : CB, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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4 citing papers in PubMed.
- Polygenic and monogenic adaptation drive evolutionary rescue at different magnitudes of environmental change.The Journal of heredity · 2026Article
- Balanced polymorphism in a floral transcription factor underlies the ancient rhythm of daily sex alternation in avocado.Proceedings of the National Academy of Sciences of the United States of America · 2026Article
- Hermaphrodite, Gonochorist, and More: Navigating the Complexities of Sex-Related Language in Biology.Integrative and comparative biology · 2026Review
- Balanced polymorphism in a floral transcription factor underlies an ancient rhythm of daily sex alternation in avocado.bioRxiv : the preprint server for biology · 2025Article
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4 authors.
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Abstract
In the angiosperm mating system of heterodichogamy, two hermaphroditic morphs temporally alternate between male and female flowering phases, promoting disassortative mating between morphs. Heterodichogamy is widespread within Juglandaceae and is controlled by distinct ancient structural variants in Juglans and Carya. Here, we identify a novel inherited basis in two additional Juglandaceae genera, Pterocarya and Cyclocarya. In Pterocarya, we map dichogamy types to an ∼70 kb trans-species structural variant overlapping a single candidate gene, GFAFL, with a dominant haplotype for female-first flowering. Heterodichogamy in Cyclocarya is associated with a distinct pair of ancient haplotypes at the same locus but with a dominant allele for male-first flowering. Both sets of alleles are ancient (ca. 45 and 50 Ma, respectively), but their divergence postdates the divergence between the genera. GFAFL expression in staminate flowers in both systems reveals trans-regulation of the recessive allele by the dominant haplotype, which in both systems contains tandem duplicates of sequence in the 3' region of GFAFL. We suggest that reciprocal sex matching in heterodichogamy can result from a combination of cis-regulatory divergence and trans-regulation involving "fast" and "slow" alleles at a single flowering-time gene, yielding "early" vs. "late" sex-specific flowering. Our findings shed light on the molecular basis of heterodichogamy and contribute to an emerging view that diverse genetic pathways can be co-opted during its evolution and facilitate turnover in its genetic control.
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