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AI-summarized plant biology research papers from bioRxiv

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Latest 7 Papers

Proline transporters balance the salicylic acid-mediated trade-off between regeneration and immunity in plants

Authors: Yang, L., Xu, D., Belew, Z. M., Cassia Ferreira Dias, N., Wang, L., Zhang, A., Chen, Y.-F. S., Newton, C. J., Kong, F., Zheng, Y., Yao, Y., Brewer, M. T., Teixeira, P. J. P. L., Nour-Eldin, H. H., Xu, D.

Date: 2025-11-20 · Version: 1
DOI: 10.1101/2025.11.20.689487

Category: Plant Biology

Model Organism: Multi-species

AI Summary

The study identifies wound‑induced proline transporters ProT2 and ProT3 as central regulators that link salicylic acid signaling to the suppression of de novo root regeneration (DNRR) via modulation of reactive oxygen species dynamics. Genetic loss of these transporters or pharmacological inhibition of proline transport alleviates SA‑mediated regeneration inhibition across several plant species without compromising disease resistance.

salicylic acid proline transporters de novo root regeneration reactive oxygen species immunity‑regeneration trade‑off

Rubisco Dark Inhibition in Angiosperms Shows a Complex Distribution Pattern

Authors: Nehls-Ramos, C., Carmo-Silva, E., Orr, D. J.

Date: 2025-11-20 · Version: 1
DOI: 10.1101/2025.11.20.689527

Category: Plant Biology

Model Organism: Multi-species

AI Summary

The authors compiled and standardized published data on Rubisco dark inhibition for 157 flowering plant species, categorizing them into four inhibition levels and analyzing phylogenetic trends. Their meta‑analysis reveals a complex, uneven distribution of inhibition across taxa, suggesting underlying chloroplast microenvironment drivers and providing a new resource for future photosynthesis improvement efforts.

Rubisco dark inhibition flowering plants phylogenetic analysis photosynthetic regulation CO2-fixing enzyme

Developing a Molecular Toolkit to ENABLE all to apply CRISPR/Cas9-based Gene Editing in planta

Authors: Abate, B. A., Hahn, F., Chirivi, D., Betti, C., Fornara, F., Molloy, J. C., Krainer, K. M. C.

Date: 2025-11-09 · Version: 1
DOI: 10.1101/2025.11.09.687425

Category: Plant Biology

Model Organism: Multi-species

AI Summary

The authors introduce the ENABLE(R) Gene Editing in planta toolkit, a streamlined two‑step cloning system for creating CRISPR/Cas9 knockout vectors suitable for transient or stable transformation. Validation was performed in Oryza sativa protoplasts and Arabidopsis thaliana plants, and the toolkit includes low‑cost protocols aimed at facilitating adoption in the Global South.

CRISPR/Cas9 plant gene editing low‑cost cloning Global South agriculture ENABLE(R) toolkit

A plant-centric investigation of Class B Flavin-dependent Monooxygenase evolution and structural diversity

Authors: Christensen, J. M., Neilson, E. H.

Date: 2025-09-16 · Version: 1
DOI: 10.1101/2025.09.16.676513

Category: Plant Biology

Model Organism: Multi-species

AI Summary

The study presents a plant‑focused phylogenetic analysis of class B flavin‑dependent monooxygenases, identifying eight distinct families and revealing lineage‑specific diversification, especially in the NADPH‑binding domain. Using known FMOs as baits, they assembled flavin‑related proteins from key Viridiplantae lineages, performed domain architecture and motif analyses, and reclassified several families, providing a framework for future functional studies.

Class B flavin-dependent monooxygenases phylogenetic analysis Viridiplantae domain architecture motif analysis

The secreted redox sensor roGFP2-Orp1 reveals oxidative dynamics in the plant apoplast

Authors: Ingelfinger, J., Zander, L., Seitz, P. L., Trentmann, O., Tiedemann, S., Sprunck, S., Dresselhaus, T., Meyer, A. J., Müller-Schüssele, S. J.

Date: 2025-07-09 · Version: 2
DOI: 10.1101/2025.01.10.632316

Category: Plant Biology

Model Organism: Multi-species

AI Summary

The study evaluated the genetically encoded redox biosensor roGFP2-Orp1 for monitoring extracellular redox dynamics in diverse land plants, revealing that re‑oxidation rates in the apoplast differ between Physcomitrium patens and Arabidopsis thaliana and are accelerated by immune activation. Comparisons across tip‑growing cells showed no intracellular redox gradient but a partially reduced extracellular sensor in Nicotiana tabacum pollen tubes, indicating species‑ and cell‑type‑specific oxidative processes.

reactive oxygen species apoplastic redox dynamics roGFP2-Orp1 biosensor immune signaling plant model species

The auxin gatekeepers: Evolution and diversification of the YUCCA family

Authors: Vijayanathan, M., Faryad, A., Abeywickrama, T. D., Christensen, J. M., Neilson, E. H.

Date: 2025-04-14 · Version: 1
DOI: 10.1101/2025.04.11.648386

Category: Plant Biology

Model Organism: Multi-species

AI Summary

The authors conducted a comprehensive phylogenetic and sequence analysis of the conserved YUCCA (YUC) gene family across representative plant lineages, classifying the family into six major classes and 41 subclasses. They linked YUC diversification to protein sequence conservation and spatial/temporal gene expression patterns, providing a framework for future functional investigations of auxin biosynthesis.

YUCCA gene family indole-3-acetic acid phylogenetic analysis gene family diversification auxin biosynthesis

A drought stress-responsive metabolite malate modulates stomatal responses through G-protein-dependent pathway in grapevine and Arabidopsis

Authors: Mimata, Y., Gong, R., Pei, X., Qin, G., Ye, W.

Date: 2025-02-27 · Version: 2
DOI: 10.1101/2024.04.02.587830

Category: Plant Biology

Model Organism: Multi-species

AI Summary

The study examined how tricarboxylic acid (TCA) cycle metabolites influence drought tolerance in grapevine and Arabidopsis, finding that malate uniquely triggers stomatal closure via elevations in cytosolic Ca2+ and activation of the SLAC1 anion channel. G-proteins were shown to be essential for malate‑mediated signaling, linking metabolic changes to drought response through a second‑messenger cascade.

drought stress TCA cycle metabolites malate signaling guard cells G‑protein