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Zoller, D.

Publications and source records attributed to Zoller, D..

2 recordsLinked to original sources

Distinct nanoscale dynamics of growth receptor complexes link hormone perception to rapid cell wall remodeling

Cell elongation is a fundamental process allowing plants to change size and shape, a process governed by several growth promoting hormones. While hormones such as brassinosteroids (BRs) and phytosulfokines (PSKs) have been shown to play important roles in elongation growth, the early steps of signal perception remains elusive, especially with regard to PSK. Here we report a rapid mechanism by which PSK alter cell wall mechanical properties in elongating hypocotyls. Notably, this mode of action differs from that of BR. Making use of atomic force microscopy and fluorescence lifetime imaging microscopy we demonstrate how hallmarks of growing plant cells such as mechanical wall properties, porosity and apoplastic pH are differentially affected by PSK compared to BR. Using super-resolution microscopy, we show that the receptor complex components for BR and PSK display individual spatiotemporal movement and organization patterns. The BR receptor BRI1 transitions to a faster diffusive state upon ligand perception, while the PSK receptor PSKR1 associates in tighter clusters. The shared co-receptor BAK1 displays a selective decrease in cluster density after PSK treatment. We found that the putative cell wall state sensor RLP44 is required for the observed changes, however the spatiotemporal dynamics of RLP44 are not altered during signaling. We propose a model of how cell walls are specifically tuned by BRI1- and PSKR1-centered signaling hubs as potential prerequisites for and during cell elongation initiation.

plant biology↗

Real-time monitoring of endogenous Fgf8a gradient attests to its role as a morphogen during zebrafish gastrulation

Morphogen gradients impart positional information to cells in a homogenous tissue field. Fgf8a, a highly conserved growth factor, has been proposed to act as a morphogen during zebrafish gastrulation. However, technical limitations have so far prevented direct visualization of the endogenous Fgf8a gradient and confirmation of its morphogenic activity. Here, we monitored Fgf8a propagation in the developing neural plate using a CRISPR/Cas9-mediated EGFP knock-in at the endogenous fgf8a locus. By combining sensitive imaging platforms with single-molecule Fluorescence Correlation Spectroscopy (FCS), we demonstrate that Fgf8a, produced at the embryonic margin, propagates by free diffusion through the extracellular space and forms a graded distribution towards the animal pole. Overlaying the Fgf8a gradient curve with expression profiles of its downstream targets determines the precise input-output relationship of Fgf8a mediated patterning. Manipulation of the Fgf8a input alters the signaling outcome, thereby establishing Fgf8a as a bona fide morphogen during zebrafish gastrulation. Furthermore, using diffusion-hindered versions of Fgf8a, we demonstrate that extracellular diffusion of the protein from the source is critical for it to achieve its morphogenic potential.

developmental biology↗