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Deubiquitinating Enzyme OTU5 Contributes to DNA Methylation Patterns and Is Critical for Phosphate Nutrition Signals1[OPEN]

The deubiqitinase OTU5 coordinates Pi deficiency signals on DNA methylation, H3K4 and H3K27 trimethylation, and gene expression, resulting in Pi-dependent root phenotypes of otu5 mutants. Phosphate (Pi) starvation induces a suite of adaptive responses aimed at recalibrating cellular Pi homeostasis....

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Bibliographic Details
Published in:Plant physiology (Bethesda) 2017-10, Vol.175 (4), p.1826-1838
Main Authors: Yen, Ming-Ren, Suen, Der-Fen, Hsu, Fei-Man, Tsai, Yi-Hsiu, Fu, Hongyong, Schmidt, Wolfgang, Chen, Pao-Yang
Format: Article
Language:English
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Summary:The deubiqitinase OTU5 coordinates Pi deficiency signals on DNA methylation, H3K4 and H3K27 trimethylation, and gene expression, resulting in Pi-dependent root phenotypes of otu5 mutants. Phosphate (Pi) starvation induces a suite of adaptive responses aimed at recalibrating cellular Pi homeostasis. Plants harboring a mutation in OVARIAN TUMOR DOMAIN-CONTAINING DEUBIQUITINATING ENZYME5 ( OTU5 ) showed altered DNA methylation of root hair-related genes and altered Pi-responsive root traits. Unlike the wild type, homozygous otu5 mutants did not respond to Pi starvation by increased lateral root formation and increased root hair length but formed very short root hairs when grown on low-Pi media. Under Pi-replete conditions, otu5 plants developed more root hairs than the wild type due to attenuated primary root growth, a phenotype that resembled that of Pi-deficient plants. Growth of plants on low-Pi media altered both H3K4 and H3K27 trimethylation levels at the transcriptional start site of a subset of genes encoding key players in Pi homeostasis, which was correlated with mRNA abundance changes of these genes. Pi starvation had a minor impact on DNA methylation. Differentially methylated regions were enriched in transposable elements, suggesting that DNA methylation associated with low Pi supply is required for maintaining genome integrity. It is concluded that DNA methylation and histone methylation constitute critical, interdependent regulatory components that orchestrate the activity of a subset of Pi-responsive genes.
ISSN:0032-0889
1532-2548
DOI:10.1104/pp.17.01188