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Biology subjects

Zemach, H.

Publications and source records attributed to Zemach, H..

2 recordsLinked to original sources

Comparative transcriptomic profile reveals candidate genes manipulated by type III effectors of Pantoea agglomerans pv. betae leading to gall formation in beet

Pantoea agglomerans pv. betae (Pab) induces tumor-like galls in beet and gypsophila, a process mediated by the secretion of effector proteins via Pabs type III secretion system (T3SS). The molecular mechanisms underlying Pab-induced gall formation remain largely unexplored. This study delves into the cellular architecture and transcriptional profile of Pab-mediated galls, comparing host responses to wild-type Pab and a T3SS-inactive mutant, hrcC-. Morphological analysis using scanning electron microscopy and cross-sectional visualization of infected beet leaf tissues revealed that Pab-induced gall-like structures are linked to cell hyperplasia and tissue ruptures, contingent on T3SS activity. Comparative transcriptome analysis of wild-type Pab and hrcC- Pab-infected beet leaves at 12 and 48 hours unveiled significant transcriptional reprogramming, with nearly 2,000 differentially expressed genes at 48 hours post inoculation. Enrichment analyses identified the upregulation of pathways related to signal transduction, defense, carbohydrate metabolism, and cell wall modulation in wild-type Pab-infected leaves compared to controls. Particularly notable was the significant upregulation of numerous genes associated with cell wall loosening by wild-type Pab, suggesting an initial rearrangement of cell wall architecture facilitates gall formation. Furthermore, transcriptome analysis demonstrated that wild-type Pab suppresses the expression of the betalain biosynthetic gene DOPA 4,5-DIOXYGENASE, leading to reduced betalain accumulation in infected tissues compared to the mutant strain. These findings offer fresh insights into the transcriptional and physiological manipulation of host tissue during the early stages of Pab-induced gall formation.

plant biology↗

A dynamic WUSCHEL / Layer 1 interplay directs shoot apical meristem formation during regeneration

De novo shoot apical meristem (SAM) organogenesis during regeneration in tissue culture has been investigated for several decades, but the precise mechanisms governing early-stage cell fate specification remain elusive. In contrast to SAM establishment during embryogenesis, in vitro SAM formation occurs without positional cues, and is characterized by spontaneous cellular patterning. Here, we have elucidated the initial stages of SAM organogenesis and the molecular mechanisms that orchestrate gene patterning to establish SAM homeostasis. We found that SAM organogenesis in tobacco calli initiates with protuberance formation followed by the formation of an intact L1 layer covering the nascent protuberance. Acquisition of L1 cellular identity is indispensable for de novo SAM formation, which also requires WUSCHEL (WUS) and the cellular capacity to direct anticlinal cell divisions. An intriguing finding is that TONNEAU1 silencing prevents the exclusive occurrence of anticlinal divisions in the outermost layer of the protuberances and suppresses the acquisition of L1 cellular identity, ultimately impeding regeneration. This study exposes an intricate interplay between L1 and WUS expression and that any disruption in this interplay compromises shoot formation. It further provides a novel molecular framework for the characterization of WUS/L1 interplay-mediated shoot apical meristem formation during regeneration.

plant biology↗