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Cell wall heterogeneity during root growth

Applicant Dr. Marc Somssich
Subject Area Plant Cell and Developmental Biology
Plant Genetics and Genomics
Plant Physiology
Term from 2016 to 2020
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 344523413
 
Final Report Year 2020

Final Report Abstract

The plant cell wall is a highly complex structure, made up mostly of different polysaccharides, the main ones being cellulose, hemicellulose and pectin. In generalized models of plant cell walls, cellulose is depicted as long microfibrils, which act as the load bearing scaffold of the wall. The cellulose microfibrils are interconnected by hemicelluloses (xyloglucans in primary cell walls; xylans in secondary walls), which provide additional stability. The large group of pectic polysaccharides form an amorphous matrix, which embeds the cellulose-hemicellulose structure and seals off the wall. While this model is generally correct, it must also be assumed that cell walls of cells in different developmental stages, or with different specializations, have different structural properties and compositions. In this project we set out to analyse such differences. We subjected plants to different stimuli, which we expected to impact the plant cell wall, such as changes in the plants graviresponse, induced cell wall synthesis in cells lacking a wall, changes to the environment, or a pathogenic attack. We found that the cell’s response to changes in the gravitropic vector includes re-orientation of the cellulose microfibrils and changes in hemicellulosic mannan content, both affecting the walls stiffness and allowing the plant to adjust its growth according to the changes in graviperception. We also identified a master transcriptional regulator triggering the primary cell wall synthesis program, which we used to induce primary cell walls in cell regions that would normally form secondary cell walls. Using this we found that some aspects of cell wall synthesis are guided by such a developmental switch, while others are directed by the cell’s environment. Analysing plant mutants for a putative cell wall integrity sensor, we identified a pathway that adjusts cell growth to changes in environmental pH, by regulating proton-pumps and calcium-influx, thereby neutralizing a pH gradient that formed across the plasma membrane because of the acidification of the environment. Finally, we initiated a project visualizing damages done to the cell wall by a fungal pathogen, as well as the cell’s response to these damages, using custom-built microscopic tools. We believe that the work done in this project will contribute to a more detailed understanding of plant cell wall structure, which will eventually show that plant cell walls are not just a homogenous barrier, but a sensory platform with complex heterogeneities between different cells and cell types.

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