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Societal Impact Statement Rafflesiais a genus of parasitic plants with the largest flowers in the world, unique to the threatened forest habitats of tropical Asia. Here, we report on genes that are active (the transcriptome) inRafflesiaseeds as part of a larger effort to understandRafflesia.Rafflesiahas never been grown successfully outside of its native range. Consequently, seed banking is not yet possible, precluding a critical management strategy for conservation. The study ofRafflesiaseed biology is a critical step to improve its cultivation, which will educate the public about unique species and the importance of conserving their habitats. SummaryRafflesiais of great interest as one of the only two plants known to have completely lost its chloroplast genome.Rafflesiais a holoparasite and an endophyte that lives inside the tissues of its host, a tropical grape vine (Tetrastigma), emerging only to bloom—with the largest flower of any plant. Here, we report the firstRafflesiaseed transcriptome and compare it with those of other plants to deepen our understanding of its extraordinary life history.We assembled a transcriptome from RNA extracted from seeds of the Philippine endemicRafflesia speciosaand compared this with those of other plants, includingArabidopsis, parasitic plantsStrigaandCuscuta, and the mycoheterotrophic orchidAnoectochilus.Genetic and metabolic seed pathways inRafflesiawere generally similar to the other plant species. However, there were some notable exceptions. We found evidence of horizontal transfer of a gene potentially involved in circumventing host defenses. Moreover, we identified a possible convergence among parasitic plants becauseRafflesia,Striga, andCuscutashared important similarities. We were unable to find evidence of genes involved in mycorrhizal symbiosis, suggesting that mycoheterotrophy is unlikely to play a role inRafflesiaparasitism.To date, ex situ propagation ofRafflesiaby seed has been mostly unsuccessful. Our research is a bold step forward in understanding the fundamentals ofRafflesiaseed biology that will inform the continued propagation and seed‐banking efforts concerning this recalcitrant plant. We discuss our findings in the broader context of the conservation of a genus in peril. 

Abstract Angiosperms are the cornerstone of most terrestrial ecosystems and human livelihoods^1,2. A robust understanding of angiosperm evolution is required to explain their rise to ecological dominance. So far, the angiosperm tree of life has been determined primarily by means of analyses of the plastid genome^3,4. Many studies have drawn on this foundational work, such as classification and first insights into angiosperm diversification since their Mesozoic origins^5–7. However, the limited and biased sampling of both taxa and genomes undermines confidence in the tree and its implications. Here, we build the tree of life for almost 8,000 (about 60%) angiosperm genera using a standardized set of 353 nuclear genes⁸. This 15-fold increase in genus-level sampling relative to comparable nuclear studies⁹provides a critical test of earlier results and brings notable change to key groups, especially in rosids, while substantiating many previously predicted relationships. Scaling this tree to time using 200 fossils, we discovered that early angiosperm evolution was characterized by high gene tree conflict and explosive diversification, giving rise to more than 80% of extant angiosperm orders. Steady diversification ensued through the remaining Mesozoic Era until rates resurged in the Cenozoic Era, concurrent with decreasing global temperatures and tightly linked with gene tree conflict. Taken together, our extensive sampling combined with advanced phylogenomic methods shows the deep history and full complexity in the evolution of a megadiverse clade.