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Reyes-Hernandez, J.

Publications and source records attributed to Reyes-Hernandez, J..

2 recordsLinked to original sources

Spatiotemporal Dynamics of Anionic Phospholipids Orchestrate Lateral Root Initiation and Morphogenesis in Arabidopsis thaliana

Lateral root (LR) development in Arabidopsis thaliana requires precise coordination of pericycle founder cell (FC) specification, patterning, and morphogenesis. While auxin signalling is well established in this process, the role of membrane lipid signalling--particularly phosphoinositides--remains less understood. Here, we investigate the contribution of the anionic phospholipids PI4P, PI(4,5)P2, and phosphatidylserine (PS) to LR formation using live-cell biosensors, genetic mutants, and inducible lipid depletion tools. We show that PI4P is uniformly distributed throughout lateral root primordia (LRPs), whereas PI(4,5)P2 is specifically depleted in the proliferative core during early LRP development. Time-lapse imaging revealed stable PI4P and PI(4,5)P2 levels before and after FC activation, while PS increased rapidly post-activation. In xylem-pole pericycle (XPP) cells, PI(4,5)P2 decreased and PS increased following LR initiation, with both changes occurring in a membrane-domain-specific manner. Genetic analysis of the pip5k1pip5k2 double mutant, deficient in PI(4,5)P2 synthesis, revealed impaired LR initiation and emergence. Conversely, inducible depletion of PI(4,5)P2 using the iDePP system enhanced LRP initiation and accelerated development when activated after FC specification. These results suggest that PI4P functions as a stable basal lipid, while PI(4,5)P2 and PS undergo dynamic, spatially regulated changes critical for LR progression. Notably, PI(4,5)P2 acts as a negative regulator of LRP initiation and morphogenesis. Our findings highlight how lipid signalling, in coordination with hormonal cues, provides spatial and temporal control over pericycle cell behaviour and lateral root organogenesis. SIGNIFICANCE STATEMENTThis study reveals how specific membrane lipids help control where and when new lateral roots form in plants. While plant hormones like auxin are known to guide root branching, this work shows that lipids such as PI(4,5)P2 and phosphatidylserine also play key roles. Using live imaging and genetic tools, we found that reducing PI(4,5)P2 in certain root cells promotes root growth by triggering cell division and development. In contrast, phosphatidylserine level increases right when root-forming cells become active. These discoveries highlight a new layer of control in plant development and suggest that lipids help fine-tune the formation of roots, which is essential for how plants take up water and nutrients.

plant biology↗

GreenGate 2.0: backwards compatible addons for assembly of complex transcriptional units and their stacking with GreenGate

Molecular cloning is a crucial technique in genetic engineering that enables the precise design of synthetic transcriptional units (TUs) and the manipulation of genomes. GreenGate and several other modular molecular cloning systems were developed about ten years ago and are widely used in plant research. All these systems define grammars for assembling transcriptional units from building blocks, cloned as Level 0 modules flanked by four-base pair overhangs and recognition sites for a particular Type IIs endonuclease. Modules are efficiently assembled into Level 1 TUs in a hierarchical assembly process, and Level 2 multigene constructs are assembled by stacking Level 1 TUs. GreenGate is highly popular but has three main limitations. First, using ad-hoc overhangs added by PCR and classical restriction/ligation prevents the efficient use of a one-pot, one-step reaction to generate entry clones and domesticate internal sites; second, a Level 1 TU is assembled from a maximum of six modules, which may be limiting for applications such as multiplex genome editing; third, the generation of Level 2 assemblies is sequential and inefficient. GreenGate 2.0 (GG2.0) expands GreenGate features. It introduces additional overhangs, allowing for the combination of up to 12 Level 0 modules in a Level 1 TU. It includes a Universal Entry Generator plasmid (pUEG) to streamline the generation of Level 0 modules. GG2.0 introduces GreenBraid, a convenient method for stacking transcriptional units iteratively for multigene assemblies. Importantly, GG2.0 is backwards compatible with most existing GreenGate modules. Additionally, GG2.0 includes Level 0 modules for multiplex expression of guide RNAs for CRISPR/Cas9 genome editing and pre-assembled Level 1 vectors for dexamethasone-inducible gene expression and ubiquitous expression of plasma membrane and nuclear fluorescent markers. GG2.0 streamlines and increases the versatility of assembling complex transcriptional units and their combination.

plant biology↗