Please use this identifier to cite or link to this item:
https://doi.org/10.1371/journal.ppat.1004972
Title: | Twilight, a Novel Circadian-Regulated Gene, Integrates Phototropism with Nutrient and Redox Homeostasis during Fungal Development | Authors: | Deng Y.Z. Qu Z. Naqvi N.I. |
Keywords: | transcription factor SNF fungal protein acetylation Article circadian rhythm controlled study darkness fungal development fungal gene fungal metabolism genetic regulation habitual adaptation homeostasis Magnaporthe oryzae nonhuman phosphorylation phototropism Twilight gene circadian rhythm drug effects food fungus hyphae fungus spore gene expression regulation genetics growth, development and aging homeostasis light Magnaporthe metabolism microbiology Oryza oxidation reduction reaction phototropism physiology plant disease Fungi Magnaporthe grisea Magnaporthe oryzae Circadian Rhythm Food Fungal Proteins Gene Expression Regulation, Fungal Homeostasis Hyphae Light Magnaporthe Oryza Oxidation-Reduction Phototropism Plant Diseases Spores, Fungal |
Issue Date: | 2015 | Publisher: | Public Library of Science | Citation: | Deng Y.Z., Qu Z., Naqvi N.I. (2015). Twilight, a Novel Circadian-Regulated Gene, Integrates Phototropism with Nutrient and Redox Homeostasis during Fungal Development. PLoS Pathogens 11 (6) : e1004972. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.ppat.1004972 | Abstract: | Phototropic regulation of circadian clock is important for environmental adaptation, organismal growth and differentiation. Light plays a critical role in fungal development and virulence. However, it is unclear what governs the intracellular metabolic response to such dark-light rhythms in fungi. Here, we describe a novel circadian-regulated Twilight (TWL) function essential for phototropic induction of asexual development and pathogenesis in the rice-blast fungus Magnaporthe oryzae. The TWL transcript oscillates during circadian cycles and peaks at subjective twilight. GFP-Twl remains acetylated and cytosolic in the dark, whereas light-induced phosphorylation (by the carbon sensor Snf1 kinase) drives it into the nucleus. The mRNA level of the transcription/repair factor TFB5, was significantly down regulated in the twl∆ mutant. Overexpression of TFB5 significantly suppressed the conidiation defects in the twl∆ mutant. Furthermore, Tfb5-GFP translocates to the nucleus during the phototropic response and under redox stress, while it failed to do so in the twl∆ mutant. Thus, we provide mechanistic insight into Twl-based regulation of nutrient and redox homeostasis in response to light during pathogen adaptation to the host milieu in the rice blast pathosystem. © 2015 Deng et al. | Source Title: | PLoS Pathogens | URI: | https://scholarbank.nus.edu.sg/handle/10635/165390 | ISSN: | 15537366 | DOI: | 10.1371/journal.ppat.1004972 |
Appears in Collections: | Staff Publications Elements |
Show full item record
Files in This Item:
File | Description | Size | Format | Access Settings | Version | |
---|---|---|---|---|---|---|
10_1371_journal_ppat_1004972.pdf | 5 MB | Adobe PDF | OPEN | None | View/Download |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.