Proceedings of the National Academy of Sciences · 2007 · 134 citations · 43 references
Life SciencesEvolutionary BiologyPlant SciencesEmbryogenesisOrganogenesisPlant EvolutionAsexual ReproductionEmbryo DevelopmentEvolution Of Plant DevelopmentLeaf DevelopmentSeed DevelopmentSomatic EmbryogenesisAncestral Developmental TraitsAsexual Reproduction EvolutionEmbryogenesis EvolutionLeaf MarginsLeaf OrganogenesisRegulatorsSexual Reproduction EvolutionSexual Reproduction In Plants
Plant somatic cells have the remarkable ability to regenerate an entire organism. Many species in the genus Kalanchoë, known as "mother of thousands," develop plantlets on the leaf margins. Using key regulators of organogenesis (STM) and embryogenesis (LEC1 and FUS3) processes, we analyzed asexual reproduction in Kalanchoë leaves. Suppression of STM abolished the ability to make plantlets. Here, we report that constitutive plantlet-forming species, like Kalanchoë daigremontiana, form plantlets by coopting both organogenesis and embryogenesis programs into leaves. These species have a defective LEC1 gene and produce nonviable seed, whereas species that produce plantlets only upon stress induction have an intact LEC1 gene and produce viable seed. The latter species are basal in the genus, suggesting that induced-plantlet formation and seed viability are ancestral traits. We provide evidence that asexual reproduction likely initiated as a process of organogenesis and then recruited an embryogenesis program into the leaves in response to loss of sexual reproduction within this genus.
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A member of the KNOTTED class of homeodomain proteins encoded by the STM gene of Arabidopsis
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