4.8 Article

Mechanical Shielding in Plant Nuclei

Journal

CURRENT BIOLOGY
Volume 30, Issue 11, Pages 2013-+

Publisher

CELL PRESS
DOI: 10.1016/j.cub.2020.03.059

Keywords

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Funding

  1. Centre National de la Recherche Scientifique (CNRS)
  2. Fondation Schlumberger pour l'Education et la Recherche (FSER)
  3. European Research Council [ERC-2013-CoG-615739]
  4. IdEX international PhD program (unista, Strasbourg)
  5. HFSP grant 2018, RGP [009]
  6. labex Who AM I ? [labex ANR-11-LABX-0071]
  7. Universite de Paris, - French Government through its Investments for the Future program [Idex ANR-18IDEX-0001]
  8. COST Action INDEPTH network [CA1612]

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In animal single cells in culture, nuclear geometry and stiffness can be affected by mechanical cues, with important consequences for chromatin status and gene expression. This calls for additional investigation into the corresponding physiological relevance in a multicellular context and in different mechanical environments. Using the Arabidopsis root as a model system, and combining morphometry and micro-rheometry, we found that hyperosmotic stress decreases nuclear circularity and size and increases nuclear stiffness in meristematic cells. These changes were accompanied by enhanced expression of touch response genes. The nuclear response to hyperosmotic stress was rescued upon return to iso-osmotic conditions and could even lead to opposite trends upon hypo-osmotic stress. Interestingly, nuclei in a mutant impaired in the functions of the gamma-tubulin complex protein 3 (GCP3) interacting protein (GIP)/MZT1 proteins at the nuclear envelope were almost insensitive to such osmotic changes. The gip1gip2 mutant exhibited constitutive hyperosmotic stress response with stiffer and deformed nuclei, as well as touch response gene induction. The mutant was also resistant to lethal hyperosmotic conditions. Altogether, we unravel a stereotypical geometric, mechanical, and genetic nuclear response to hyperosmotic stress in plants. Our data also suggest that chromatin acts as a gel that stiffens in hyperosmotic conditions and that the nuclear-envelope-associated protein GIPs act as negative regulators of this response.

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