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Han, T.-S.

Publications and source records attributed to Han, T.-S..

3 recordsLinked to original sources

A 3D framework for delimiting a polyploid complex in Rorippa (Brassicaceae): combining trait evolution, herbarium records, and machine learning

Species delimitation in polyploid complexes remains a fundamental challenge due to pervasive morphological overlap and genomic redundancy. We examined the Rorippa dubia-indica complex (Brassicaceae), a polyploid lineage comprising tetraploid and hexaploid taxa. We developed an integrative 3D framework (Delimitation, Distribution, and Decoding) that synthesizes spatiotemporal data from field (2017-2020; n = 3,136) and herbarium (1893-2021; n = 2,015) collections to diagnose misidentification, model distributions, and reconstruct classification criteria used in polyploid complexes. Morphological traits with varying degrees of plasticity were evaluated under controlled conditions to identify stable diagnostic characters. Seed arrangement, petal number, and genome size or ploidy level exhibited clear interspecific differentiation. Phylogenomic analyses based on chloroplast genomes further defined species boundaries clarified by these taxonomic traits. We then revised herbarium specimens and applied machine learning classification models to assess the extent of specimen misidentification and to recover the trait-based rationale behind species assignments. Initial misidentification rates reached 12-50% across virtual or physical specimens, largely due to reliance on plastic traits. These errors substantially distorted spatial distribution models and future climate projections. Our findings underscore the need for secondary specimen evaluation and demonstrate the importance of integrating morphologic and phylogenetic inference with machine learning tools to resolve morphologically overlapping polyploid complexes. This approach offers direct applications for biodiversity assessment, evolutionary research, and conservation planning.

systems biology↗

Intraspecific genome size variation in Rorippa indica reveals a tropical adaptation by genomic enlargement

Genome size exhibits substantial variation across organisms, but the underlying causes and ecological consequences remain unclear. While interspecific comparisons have suggested selective pressures against large genomes, intraspecific variation has been less explored. Here, we investigate genome size variation within the hexaploid yellowcress herb, Rorippa indica, by integrating flow cytometry, plastomic phylogeography, genomic repeat profiling, and reciprocal common garden experiments. We analyzed 192 accessions from 83 natural populations, revealing a 128 Mb range in genome size. Plastome haplotype analysis identified a haplogroup that shifted niches to tropics and evolved larger genomes. A strong correlation was found between larger genomes and tropical habitats characterized by higher temperatures and lower seasonality. Genomic repeat content, particularly 45S rDNA and Ty1-copia transposable elements, was associated with larger genomes. Reciprocal transplantation experiments confirmed the adaptive nature of large genomes in tropical environments, with individuals exhibiting lower growth rates but higher fecundity. Our findings support the "large genome selection" hypothesis, suggesting that genome size enlargement, driven by genomic repetitive elements, can be an adaptive response to high temperatures of tropics. As global warming continues, plants with larger genomes may exhibit slower growth but increased reproductive output, potentially impacting ecosystem dynamics and agricultural productivity.

evolutionary biology↗

Darapladib, an inhibitor of Lp-PLA2, sensitizes cancer cells to ferroptosis by remodeling lipid metabolism

Arachidonic and adrenic acids in the membrane play key roles in ferroptosis, but how these fatty acids are manipulated in cells is largely unknown. Here, we reveal that lipoprotein-associated phospholipase A2 (Lp-PLA2) controls intracellular phospholipid metabolism and contributes to ferroptosis resistance. A metabolic drug screen identified that darapladib (SB-480848), an inhibitor of Lp-PLA2, synergistically induced ferroptosis with GPX4 inhibitors. Notably, darapladib was able to enhance ferroptosis under lipoprotein-deficient or serum-free conditions. Furthermore, Lp-PLA2 was located in the membrane and cytoplasm and suppressed ferroptosis, suggesting the critical role of intracellular Lp-PLA2. Lipidomic analysis showed that phosphatidylethanolamine (PE) species were generally enriched, while lysophosphatidylethanolamine (lysoPE) and free fatty acid levels were reduced, upon darapladib treatment. Finally, combination treatment with darapladib and PACMA31, a GPX4 inhibitor, efficiently inhibited tumor growth in a xenograft model. Our study suggests that inhibition of Lp-PLA2 is a potential therapeutic strategy to enhance ferroptosis in cancer treatment.

cancer biology↗