LAUSR

Rice (Oryza sativa) is one of the most important staple crops worldwide, providing 420% of the calories to over 3.5 billion people (Wing et al., 2018). Cadmium (Cd) is a toxic heavy metal that affects the growth and metabolism of plants. Exposure to Cd is also linked to potential health risks in humans (Hayat et al., 2019). Most nonwork-related Cd exposure is associated with food, with rice being a major source of human Cd intake. Hence, understanding Cd accumulation mechanisms in rice could enable controlling Cd content in rice grains (Clemens and Ma, 2016). Cd uptake by roots and its translocation within a plant are tightly regulated by transporter activity. To date, several transporter proteins associated with Cd uptake in roots have been identified, including Natural ResistanceAssociated Macrophage Protein 5 and 1 (OsNRAMP5/1) and the major facilitator family protein OsCd1 (Sasaki et al., 2012; Yan et al., 2019; Chang et al., 2020). Another Cd transporter, OsHMA3 (Heavy Metal ATPase 3), localizes to the tonoplast membrane of rice root cells and participates in Cd sequestration into root vacuoles, thereby preventing Cd toxicity in aerial plant parts (Ueno et al., 2010). OsLCT1 (Low-affinity Cation Transporter 1), a low-affinity cation transporter, mediates Cd loading into the phloem, regulating Cd transport into rice grains (Uraguchi et al., 2011). However, no phloem unloading transporters have been identified to date. In this issue of the Plant Physiology, Tian-Yu Gu and colleagues (Gu et al. 2022) demonstrate the role of defensin family member DEF8 as a mediator of xylem Cd loading and phloem Cd unloading in rice. Defensins are a group of cysteine-rich proteins composed of the cysteine-rich domain that can bind to metal ions and the secretion signal peptide (SSP). Several defensin-like proteins play a role in Cd transport and distribution, suggesting that other defensin family members could play important roles in Cd translocation within a plant (Luo et al., 2018). First, the authors studied gene expression profiles of all rice defensin family genes. DEFENSIN 8 (DEF8) was selected for further characterization due to its high expression levels in rice endosperm. DEF8 expression was upregulated in seeds through maturation and in roots during Cd exposure, suggesting that DEF8 participates in rice grain Cd loading. Histochemical analysis showed that DEF8 was expressed in the roots and shoots of rice seedlings, specifically in phloem and pericycle cells (Figure 1). Fluorescently tagged DEF8 localized to cell walls of rice sheath and onion (Allium cepa) epidermis cells. Interestingly, when the SSP domain sequence was removed, DEF8 re-localized to the cytosol, indicating that the SSP domain is indispensable for DEF8 efflux. Taken together, DEF8 tissue and subcellular localization indicated its possible role in Cd long-distance transport. Plant treatment with BrefeldinA, a vesicular transport inhibitor, led to the formation of vesicle bodies in Arabidopsis thaliana roots, suggesting that DEF8 could be secreted through the vesicle trafficking pathway. Binding assays with recombinant full-length and mature (lacking SSP domain) DEF8 at acidic and neutral pH showed Cd chelation activity, indicating that DEF8 could mediate Cd transport to the apoplast via chelation and secretion. To determine the role of DEF8 in rice plants, the authors created DEF8 overexpression and knockout lines. The mutant lines and respective wild-type controls were hydroponically grown in media supplemented with Cd. Plants overexpressing DEF8 had lower levels of Cd in roots and N ew s an d V ie w s