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Zahurancik, W. J.

Publications and source records attributed to Zahurancik, W. J..

2 recordsLinked to original sources

Stress Granule Protein TZF1 Enhances Salt Stress Tolerance by Targeting ACA11 mRNA for Degradation in Arabidopsis

Tandem CCCH zinc finger (TZF) proteins play diverse roles in plant growth and stress response. Although as many as 11 TZF proteins have been identified in Arabidopsis, little is known about the mechanism by which TZF proteins select and regulate the target mRNAs. Here, we report that Arabidopsis TZF1 is a bona-fide stress granule protein. Ectopic expression of TZF1 (TZF1 OE), but not an mRNA binding-defective mutant (TZF1H186Y OE), enhances salt stress tolerance in Arabidopsis. RNA-seq analyses of NaCl-treated plants revealed that the down-regulated genes in TZF1 OE plants are enriched for functions in salt and oxidative stress responses. Because many of these down-regulated mRNAs contain AU- and/or U-rich elements (AREs and/or UREs) in their 3-UTRs, we hypothesized that TZF1--ARE/URE interaction might contribute to the observed gene expression changes. Results from RNA immunoprecipitation-quantitative PCR analysis, gel-shift, and mRNA half-life assays indicate that TZF1 binds and triggers degradation of the autoinhibited Ca2+-ATPase 11 (ACA11) mRNA, encoding a tonoplast-localized calcium pump that extrudes calcium and dampens the signal transduction pathways necessary for salt stress tolerance. Furthermore, this salt stress-tolerance phenotype was recapitulated in aca11 null mutants. Remarkably, a set of positive regulators for salt stress tolerance was upregulated in TZF1 OE plants. These include Na+/H+ Exchanger (NHX) family members known to contribute to Na+ homeostasis and salinity stress tolerance. Collectively, we present a model in which TZF1 targets ACA11 and ACA4 directly, and repressors of NHXs and other negative regulators indirectly for mRNA degradation to enhance plant salt stress tolerance.

plant biology↗

RNAs undergo phase transitions with lower critical solution temperatures

Co-phase separation of RNAs and RNA-binding proteins is thought to drive the biogenesis of ribonucleoprotein granules. RNAs can also undergo phase transitions in the absence of proteins. However, the physicochemical driving forces of protein-free, RNA-driven phase transitions remain unclear. Here, we report that RNAs of various types undergo phase transitions with system-specific lower critical solution temperatures (LCSTs). This entropically-driven phase behavior requires Mg2+ ions and is an intrinsic feature of the phosphate backbone that is modulated by RNA bases. RNA-only condensates can additionally undergo enthalpically favorable percolation transitions within dense phases. This is enabled by a combination of Mg2+-dependent bridging interactions among phosphate groups and RNA base-stacking / base-pairing. Phase separation coupled to percolation can cause dynamical arrest of RNAs within condensates and can suppress the catalytic activity of an RNase P ribozyme. Our work highlights the need to incorporate RNA-driven phase transitions into models for RNP granule biogenesis.

biophysics↗