Transfer cells are characterized by wall labyrinths with either a flange or reticulate architecture. A literature survey established that reticulate wall ingrowth papillae ubiquitously arise from a modified component of their wall labyrinth, termed the uniform wall layer; a structure absent from flange transfer cells. This finding sparked an investigation of the deposition characteristics and role of the uniform wall layer using a cotyledon culture system. On transfer of cotyledons to culture, their adaxial epidermal cells spontaneously -differentiate to a reticulate architecture comparable to their abaxial epidermal transfer cell counterparts formed . Uniform wall layer construction commenced once adaxial epidermal cell expansion had ceased to overlay the original outer periclinal wall on its inner surface. In contrast to the dense ring-like lattice of cellulose microfibrils in the original primary wall, the uniform wall layer was characterized by a sparsely dispersed array of linear cellulose microfibrils. A re-modeled cortical microtubule array exerted no influence on uniform wall layer formation or on its cellulose microfibril organization. Surprisingly, formation of the uniform wall layer was not dependent upon depositing a cellulose scaffold. In contrast, uniform wall cellulose microfibrils were essential precursors for constructing wall ingrowth papillae. On converging to form wall ingrowth papillae, the cellulose microfibril diameters increased 3-fold. This event correlated with up-regulated differential, and transfer-cell specific, expression of while transcript levels of other cellulose biosynthetic-related genes linked with primary wall construction were substantially down-regulated.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723425PMC
http://dx.doi.org/10.3389/fpls.2017.02035DOI Listing

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