The study combined cell biology, transcriptomics, and ionomics to reveal that zinc deficiency reduces root apical meristem size while preserving meristematic activity and local Zn levels, leading to enhanced cell elongation and differentiation in Arabidopsis thaliana. ZIP12 was identified as a highly induced gene in the zinc‑deficient root tip, and zip12 mutants displayed impaired root growth, altered RAM structure, disrupted Zn‑responsive gene expression, and abnormal metal partitioning, highlighting ZIP12’s role in maintaining Zn homeostasis and meristem function.
Multi-Omics Analysis of Heat Stress-Induced Memory in Arabidopsis
Authors: Thirumlaikumar, V. P. P., Yu, L., Arora, D., Mubeen, U., Wisniewski, A., Walther, D., Giavalisco, P., Alseekh, S., DL Nelson, A., Skirycz, A., Balazadeh, S.
The study uses a high‑throughput comparative multi‑omics strategy to profile transcript, metabolite, and protein dynamics in Arabidopsis thaliana seedlings throughout the heat‑stress memory (HSM) phase following acquired thermotolerance. Early recovery stages show rapid transcriptional activation of memory‑related genes, while protein levels stay elevated longer, and distinct metabolite patterns emerge, highlighting temporal layers of the memory process.
Molecular and Phenotypic Characterization of Telomere Repeat Binding (TRBs) Proteins in Moss: Evolutionary and Functional Perspectives
Authors: Kusova, A., Hola, M., Goffova Petrova, I., Rudolf, J., Zachova, D., Skalak, J., Hejatko, J., Klodova, B., Prerovska, T., Lycka, M., Sykorova, E., Bertrand, Y. J. K., Fajkus, J., Honys, D., Prochazkova Schrumpfova, P.
The study characterizes telomere repeat binding (TRB) proteins in the model moss Physcomitrium patens, demonstrating that individual PpTRB genes are essential for normal protonemal and gametophore development and that loss of TRBs leads to telomere shortening, mirroring findings in seed plants. Transcriptome analysis of TRB mutants shows altered expression of genes linked to transcription regulation and stimulus response, while subcellular localization confirms nuclear residence and mutual interaction of PpTRBs, underscoring their conserved role in telomere maintenance across land plants.
The study used transcriptomic and lipidomic profiling to investigate how chia (Salvia hispanica) leaves respond to short‑term (3 h) and prolonged (27 h) heat stress at 38 °C, revealing rapid activation of calcium‑signaling and heat‑shock pathways and reversible changes in triacylglycerol levels. Nearly all heat‑responsive genes returned to baseline expression after 24 h recovery, highlighting robust thermotolerance mechanisms that could inform improvement of other oilseed crops.
Arabidopsis lines with modified ascorbate concentrations reveal a link between ascorbate and auxin biosynthesis
Authors: Fenech, M., Zulian, V., Moya-Cuevas, J., Arnaud, D., Morilla, I., Smirnoff, N., Botella, M. A., Stepanova, A. N., Alonso, J. M., Martin-Pizarro, C., Amorim-Silva, V.
The study used Arabidopsis thaliana mutants with low (vtc2, vtc4) and high (vtc2/OE-VTC2) ascorbate levels to examine how ascorbate concentration affects gene expression and cellular homeostasis. Transcriptomic analysis revealed that altered ascorbate levels modulate defense and stress pathways, and that TAA1/TAR2‑mediated auxin biosynthesis is required for coping with elevated ascorbate in a light‑dependent manner.
Comparative multi-omics profiling of Gossypium hirsutum and Gossypium barbadense fibers at high temporal resolution reveals key differences in polysaccharide composition and associated glycosyltransferases
Authors: Swaminathan, S., Lee, Y., Grover, C. E., DeTemple, M. F., Mugisha, A. S., Sichterman, L. E., Yang, P., Xie, J., Wendel, J. F., Szymanski, D. B., Zabotina, O. A.
The study performed daily large-scale glycome, transcriptome, and proteome profiling of developing fibers from the two cultivated cotton species, Gossypium barbadense and G. hirsutum, across primary and secondary cell wall stages. It identified delayed cellulose accumulation and distinct compositions of xyloglucans, homogalacturonans, rhamnogalacturonan‑I, and heteroxylans in G. barbadense, along with higher expression of specific glycosyltransferases and expansins, suggesting these molecular differences underlie the superior fiber length and strength of G. barbadense.
The study evaluated how acute heat stress affects early-stage rice seedlings, identifying a critical temperature threshold that impairs growth. Transcriptomic profiling of shoots and roots revealed ethylene‑responsive factors (ERFs) as central regulators, with ethylene and jasmonic acid acting upstream, and pre‑treatment with these hormones mitigated heat damage. These findings highlight ERF‑hormone interaction networks as targets for improving rice heat resilience.
Using the Euphorbia peplus genome, the authors performed organ‑specific transcriptomic profiling of the cyathium and combined it with gene phylogenies and dN/dS analysis to investigate floral‑development gene families. They found distinct SEP1 paralog expression, lack of E‑class gene duplications typical of other pseudanthia, and divergent expression patterns for CRC, UFO, LFY, AP3, and PI, suggesting unique developmental pathways in Euphorbia.
The study shows that heatwaves impair the ability of apple (Malus domestica) to mount ASM‑induced immunity against fire blight and apple scab, leading to a loss of protective gene expression. Transcriptomic analysis revealed a broad suppression of ASM‑regulated defense and other biological processes under high temperature, identifying thermo‑sensitive resistance and susceptibility marker genes. The findings highlight that elevated temperature both weakens plant defenses and creates a more favorable environment for pathogens.
The study employed a multi‑omics workflow (transcriptomics, ribosome profiling, and proteomics) to uncover small peptides encoded by long non‑coding RNAs (LSEPs) in rice, finding that over 40% of surveyed lncRNAs associate with ribosomes. An optimized small‑peptide extraction followed by LC‑MS/MS identified 403 LSEPs, confirming the peptide‑coding capacity of plant lncRNAs and providing a scalable pipeline for large‑scale screening.