Ceramides mediate positional signals in Arabidopsis thaliana protoderm differentiation

The differentiation of distinct cell types in appropriate patterns is a fundamental process in the development of multicellular organisms. In , protoderm/epidermis differentiates as a single cell layer at the outermost position. However, little is known about the molecular nature of the positional s...

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Published in:Development (Cambridge) Vol. 148; no. 2
Main Authors: Nagata, Kenji, Ishikawa, Toshiki, Kawai-Yamada, Maki, Takahashi, Taku, Abe, Mitsutomo
Format: Journal Article
Language:English
Published: England 25-01-2021
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Summary:The differentiation of distinct cell types in appropriate patterns is a fundamental process in the development of multicellular organisms. In , protoderm/epidermis differentiates as a single cell layer at the outermost position. However, little is known about the molecular nature of the positional signals that achieve correct epidermal cell differentiation. Here, we propose that very-long-chain fatty acid-containing ceramides (VLCFA-Cers) mediate positional signals by stimulating the function of ARABIDOPSIS THALIANA MERISTEM LAYER1 (ATML1), a master regulator of protoderm/epidermis differentiation, during lateral root development. We show that VLCFA-Cers, which are synthesized predominantly in the outermost cells, bind to the lipid-binding domain of ATML1. Importantly, this cell type-specific protein-lipid association alters the activity of ATML1 protein and consequently restricts its expression to the protoderm/epidermis through a transcriptional feedback loop. Furthermore, establishment of a compartment, enriched with VLCFA-containing sphingolipids, at the outer lateral membrane facing the external environment may function as a determinant of protodermal cell fate. Taken together, our results indicate that VLCFA-Cers play a pivotal role in directing protoderm/epidermis differentiation by mediating positional signals to ATML1.This article has an associated 'The people behind the papers' interview.
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ISSN:0950-1991
1477-9129
DOI:10.1242/dev.194969