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Burachik, N.

Publications and source records attributed to Burachik, N..

2 recordsLinked to original sources

PHYTOCHROME INTERACTING FACTORS are required to coordinate microtubule dynamics and differential cell growth during Arabidopsis apical hook opening

BackgroundDifferential cell growth is a key strategy that enables plants to adjust their morphology in response to internal and external cues. Apical hook opening in dark- grown Arabidopsis seedlings serves as an excellent model to study how coordinated cell expansion generates organ bending. Several works highlight the influence of hormone signaling, cell wall mechanics, and environmental cues on cortical microtubule (cMT) arrangement in bending tissues. However, the precise genetic hierarchy governing these processes remains largely unknown. ResultsHere, we reveal a two-step growth rate during apical hook opening, in which an initial phase of differential cell expansion is followed by a phase of more balanced growth. We show that cMT re-arrangement precedes and predicts cell expansion patterns, suggesting a central role in coordinating differential growth. Our findings indicate that PIF transcription factors regulate this process, as pifq mutants fail to align cMT reorganization with growth dynamics, resulting in premature hook opening. RNA- seq analysis further supports a role for PIFs in coordinating cell wall remodeling and microtubule-associated gene expression, including kinesins and cell wall-modifying enzymes. ConclusionsOur study uncovers a PIF-dependent regulatory mechanism that orchestrates cytoskeletal dynamics and cell expansion to control apical hook opening.

plant biology↗

RADIP LIGHT-INDUCED PHOSPHORYLATION CHANGES IN MICROTUBULE RELATED PROTEINS IN ARABIDOPSIS

Rapid hypocotyl elongation allows buried seedlings to reach the surface, where light triggers de-etiolation and inhibits hypocotyl growth mainly by phytochromes A, B and cryptochromes 1, 2. Dynamic phosphorylation/dephosphorylation events provide a mechanism to rapidly transduce light signals. Only recently we have begun to uncover the earliest phospho-signaling responders to light. Here, we report a large-scale phosphoproteomic analysis and identify 20 proteins that change their phosphorylation pattern after 20 min of white light pulse compared to darkness. Microtubule-associated proteins (MAPs) were highly overrepresented in this group. Among them, we studied CIP7 (COP1-INTERACTING-PROTEIN-7), which presented microtubule (MT) localization, in contrast to what was previously described. Phosphorylated isoform in Serine 915 (Sp915) of CIP7 was detected in etiolated seedlings but undetectable after a light pulse in the presence of photoreceptors, while its expression decays with long light exposure. The short hypocotyl phenotype and rearrangement of MTs in etiolated cip7 mutants are complemented by CIP7-YFP and the phospho-mimetic CIP7S915D-YFP, but not the phospho-null CIP7S915A-YFP suggesting that Sp915CIP7 is the active isoform that promotes hypocotyl elongation thorough MT reorganisation in darkness. Our results reveal that the small repertory of proteins that changes the phosphorylation status after a rapid light signal is tightly focused on MAPs; suggesting that phospho-regulation of microtubule-base processes are early targets during de-etiolation. The evidence on Sp915CIP7 supports this idea.

plant biology↗