Uncovering the Molecular Regulation of Seed Development and Germination in Endangered Legume Paubrasilia echinata Through Proteomic and Polyamine Analyses
Authors: Vettorazzi, R. G., Carrari-Santos, R., Sousa, K. R., Oliveira, T. R., Grativol, C., Olimpio, G., Venancio, T. M., Pinto, V. B., Quintanilha-Peixoto, G., Silveira, V., Santa-Catarna, C.
The study examined seed maturation and germination in the endangered legume Paubrasilia echinata using proteomic and polyamine analyses at 4, 6, and 8 weeks post-anthesis, identifying over 2,000 proteins and linking specific polyamines to developmental stages. Mature seeds (6 weeks) showed elevated proteasome components, translation machinery, LEA proteins, and heat shock proteins, while polyamine dynamics revealed putrescine dominance in early development and spermidine/spermine association with desiccation tolerance and germination. These findings uncover dynamic molecular shifts underlying seed development and provide insights for conservation and propagation.
The study demonstrates that limonene, a natural essential‑oil component, strongly inhibits Fusarium oxysporum, the causal agent of potato dry rot, by impairing colony growth, hyphal morphology, spore viability, membrane integrity, and transcription/translation processes, as well as disrupting ion homeostasis. Combined treatments reveal additive effects with mancozeb and synergistic effects with hymexazol, highlighting limonene's potential as an eco‑friendly bio‑fungicide for potato disease management.
The study identified lineage-specific long non‑coding RNAs (lncRNAs) from the aphid‑specific Ya gene family in Rhopalosiphum maidis and R. padi, demonstrating that these Ya lncRNAs are secreted into maize, remain stable, and move systemically. RNA interference of Ya genes reduced aphid fecundity, while ectopic expression of Ya lncRNAs in maize enhanced aphid colonization, indicating that Ya lncRNAs act as cross‑kingdom effectors that influence aphid virulence.
The study genotyped 1,013 hard red spring wheat lines using SNP arrays and targeted KASP markers to track changes in genetic diversity and the distribution of dwarfing Rht alleles over a century of North American breeding. It found shifts from Rht‑D1b to Rht‑B1b dominance, identified low‑frequency dwarf alleles at Rht24 and Rht25 that have increased recently, and revealed gene interactions that can fine‑tune plant height, along with evidence of recent selection for photoperiod sensitivity.
The study provides a comprehensive proteomic analysis of seed mitochondria from white lupin, revealing fully assembled OXPHOS complexes ready for immediate energy production upon imbibition. Quantitative mass‑spectrometry identified 1,162 mitochondrial proteins, highlighting tissue‑specific transporter and dehydrogenase profiles and dynamic remodeling during early germination, while many uncharacterized proteins suggest novel legume‑specific functions.
The study characterizes insertion mutants of the Arabidopsis thaliana CKL12 kinase, revealing its role in hypocotyl and primary root growth and indicating that the 3' end of its transcript is crucial for function. Evidence suggests CKL12 is transcriptionally regulated by brassinosteroid signaling, as its promoter binds BR-related transcription factors and their RNAi-mediated knock‑down reduces CKL12 expression, placing CKL12 downstream of BR signaling in seedling development.
Light on its feet: Acclimation to high and low diurnal light is flexible in Chlamydomonas reinhardtii
Authors: Dupuis, S., Chastain, J. L., Han, G., Zhong, V., Gallaher, S. D., Nicora, C. D., Purvine, S. O., Lipton, M. S., Niyogi, K. K., Iwai, M., Merchant, S. S.
The study examined how prior light‑acclimation influences the fitness and rapid photoprotective reprogramming of Chlamydomonas during transitions between low and high diurnal light intensities. While high‑light‑acclimated cells struggled to grow and complete the cell cycle after shifting to low light, low‑light‑acclimated cells quickly remodeled thylakoid ultrastructure, enhanced photoprotective quenching, and altered photosystem protein levels, recovering chloroplast function within a single day. Transcriptomic and proteomic profiling revealed swift induction of stress‑response genes, indicating high flexibility in diurnal light acclimation.
The study introduces a native‑condition method combining cell fractionation and immuno‑isolation to purify autophagic compartments from Arabidopsis, followed by proteomic and lipidomic characterisation of the isolated phagophore membranes. Proteomic profiling identified candidate proteins linked to autophagy, membrane remodeling, vesicular trafficking and lipid metabolism, while lipidomics revealed a predominance of glycerophospholipids, especially phosphatidylcholine and phosphatidylglycerol, defining the unique composition of plant phagophores.
The study identifies the brown planthopper salivary protein NlAnnexin-like5 (NlANX5) as a key virulence effector that disrupts rice annexin (OsANN) function, leading to altered calcium signaling and reduced plant resistance. RNAi silencing of NlANX5 impairs BPH feeding, while transgenic rice overexpressing OsANN2/OsANN8 or NlANX5 restores resistance, demonstrating an anti‑virulence breeding strategy for rice.
Gain and loss of gene function shaped the nickel hyperaccumulation trait in Noccaea caerulescens
Authors: Belloeil, C., Garcia de la Torre, V. S., Contreras Aguilera, R., Kupper, H., Lopez-Roques, C., Iampetro, C., Vandecasteele, C., Klopp, C., Launay-Avon, A., Leemhuis, W., Yamjabok, J., van den Heuvel, J., Aarts, M. G. M., Quintela Sabaris, C., Thomine, S., MERLOT, S.
The study presents a high-quality genome assembly for the nickel hyperaccumulator Noccaea caerulescens and uses it as a reference for comparative transcriptomic analyses across different N. caerulescens accessions and the non‑accumulating relative Microthlaspi perfoliatum. It identifies a limited set of metal transporters (NcHMA3, NcHMA4, NcIREG2, and NcIRT1) whose elevated expression correlates with hyperaccumulation, and demonstrates that frameshift mutations in NcIRT1 can abolish the trait, indicating an ancient, transporter‑driven origin of nickel hyperaccumulation.