4.8 Article

Uclacyanin Proteins Are Required for Lignified Nanodomain Formation within Casparian Strips

Journal

CURRENT BIOLOGY
Volume 30, Issue 20, Pages 4103-+

Publisher

CELL PRESS
DOI: 10.1016/j.cub.2020.07.095

Keywords

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Funding

  1. UK Biotechnology and Biological Sciences Research Council [BB/N023927/1]
  2. Coordinating Action in Plant Sciences promoting sustainable collaboration in plant sciences [ERA-CAPS13.089_RootBarriers]
  3. Future Food Beacon of Excellence Nottingham Research Fellowship
  4. BBSRC [BB/L027739/2, BB/N023927/1, BB/L027739/1] Funding Source: UKRI

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Casparian strips (CSs) are cell wall modifications of vascular plants restricting extracellular free diffusion into and out of the vascular system [1]. This barrier plays a critical role in controlling the acquisition of nutrients and water necessary for normal plant development [2-5]. CSs are formed by the precise deposition of a band of lignin approximately 2 mm wide and 150 nm thick spanning the apoplastic space between adjacent endodermal cells [6, 7]. Here, we identified a copper-containing protein, Uclacyanin1 (UCC1), that is sub-compartmentalized within the CS. UCC1 forms a central CS nanodomain in comparison with other CS-located proteins that are found to be mainly accumulated at the periphery of the CS. We found that loss-of-function of two uclacyanins (UCC1 and UCC2) reduces lignification specifically in this central CS nanodomain, revealing a nano-compartmentalized machinery for lignin polymerization. This loss of lignification leads to increased endodermal permeability and, consequently, to a loss of mineral nutrient homeostasis.

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