Genetius

The study compares transcriptional, proteomic, and metabolomic responses of wild‑type Arabidopsis and a cyp71A27 mutant to a plant‑growth‑promoting Pseudomonas fluorescens strain and a pathogenic Burkholderia glumeae strain, revealing distinct reprogramming and an unexpected signaling role for the non‑canonical P450 CYP71A27. Mutant analysis showed that loss of CYP71A27 alters gene and protein regulation, especially during interaction with the PGP bacterium, while having limited impact on root metabolites and exudates.

The study investigates the Arabidopsis ribosomal protein RPS6A and its role in auxin‑related root growth, revealing that rps6a mutants display shortened primary roots, fewer lateral roots, and defective vasculature that are not rescued by exogenous auxin. Cell biological observations and global transcriptome profiling show weakened auxin signaling and reduced levels of PIN auxin transporters in the mutant, indicating a non‑canonical function of the ribosomal subunit in auxin pathways.

The study reveals that auxin signaling via the cell‑surface ABP1‑TMK1 receptor complex directly phosphorylates and stabilizes the PIN2 auxin transporter, reinforcing asymmetric auxin flow during root gravitropism. Autophosphorylation of TMK1 after gravistimulation promotes its interaction with PIN2, and ABP1 functions redundantly with ABL3 upstream of TMK1, establishing a positive feedback loop essential for robust root bending.

The study investigates how miR394 influences flowering time in Arabidopsis thaliana by combining transcriptomic profiling of mir394a mir394b double mutants with histological analysis of reporter lines. Bioinformatic analysis identified a novel lncRNA overlapping MIR394B (named MIRAST), and differential promoter activity of MIR394A and MIR394B suggests miR394 fine‑tunes flower development through transcription factor and chromatin remodeler regulation.

The study shows that the Hyaloperonospora arabidopsidis effector HaRxL106 interferes with the Arabidopsis AUX/IAA protein IAA11, weakening its repressive role and thereby enhancing auxin signaling, which triggers shade‑avoidance‑like growth and concomitantly dampens immune responses. These results reveal a mechanism by which a pathogen effector co‑opts hormonal pathways to promote infection.

The study profiled the Arabidopsis apoplastic proteome during pattern‑triggered immunity induced by the flg22 peptide, using apoplastic washing fluid with minimal cytoplasmic contamination followed by LC‑MS/MS. Results showed consistent PTI‑specific enrichment and depletion of peptides, a bias toward ectodomain peptides of receptor‑like kinases, and increased abundance of the exosome marker tetraspanin 8, indicating heightened exosome levels during PTI.