| Literature DB >> 30057307 |
Pengxue Li1, Qiaozhi Yu1, Xu Gu1, Chunmiao Xu1, Shilian Qi1, Hong Wang1, Fenglin Zhong1, Tobias I Baskin2, Abidur Rahman3, Shuang Wu4.
Abstract
The Casparian strip in the root endodermis forms an apoplastic barrier between vascular tissues and outer ground tissues to enforce selective absorption of water and nutrients. Because of its cell-type specificity, the presence of a Casparian strip is used as a marker for a functional endodermis. Here, we examine the minimal regulators required for reprograming non-endodermal cells to build a functional Casparian strip. We demonstrate that the transcription factor SHORT-ROOT (SHR) serves as a master regulator and promotes Casparian strip formation through two independent activities: inducing the expression of essential Casparian strip enzymes via MYB36 and directing the subcellular localization of Casparian strip formation via SCARECROW (SCR). However, this hierarchical signaling cascade still needs SHR-independent small peptides, derived from the stele, to eventually build a functional Casparian strip in non-endodermal cells. Our study provides a synthetic approach to induce Casparian-strip-containing endodermis using a minimal network of regulators and reveals the deployment of both apoplastic and symplastic communication in the promotion of a specific cell fate.Entities:
Keywords: Casparian strip; MYB36; SCR; SHR; cell differentiation; cell-fate reprograming; cell-to-cell communication; endodermis; root; small peptide signaling
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Year: 2018 PMID: 30057307 DOI: 10.1016/j.cub.2018.07.028
Source DB: PubMed Journal: Curr Biol ISSN: 0960-9822 Impact factor: 10.834