Control of RNA polymerases I and III by the TOR signaling pathway

Insects living in the temperate zone enter a physiological state of arrested or slowed development to overcome an adverse season, such as winter. Developmental arrest, called diapause, occurs at a species-specific developmental stage, and embryonic and pupal diapauses have been extensively studied in mostly holometabolous insects. Some other insects overwinter in the nymphal stage with slow growth for which the mechanism is poorly understood. Here, we show that this nymphal period of slow growth is regulated by temperature and photoperiod through separate pathways in the cricket Modicogryllus siamensis. The former regulates the growth rate, at least in part, through the insulin / target of rapamycin (TOR) signaling pathway. Lower temperature down-regulates the expression of insulin-like peptide (Ms’Ilp) and Target of rapamycin (Ms’Tor) genes to slow down the growth rate without affecting the number of molts. The latter regulates the number of molts independent of temperature. Short days increase the number of molts through activation of the juvenile hormone (JH) pathway and down-regulation of myoglianin (Ms’myo), a member of the TGFβ family, which induces adult metamorphosis. In contrast, long days regulate Ms’myo expression to increase during the fifth to sixth instar to initiate adult metamorphosis. When Ms’myo expression is suppressed, juvenile hormone O-methyl transferase (Ms’jhamt) was up-regulated and increased molts to prolong the nymphal period even under long-day conditions. The present findings suggested that the photoperiod regulated Ms’myo, and the JH signaling pathway and the temperature-controlled insulin/TOR pathway cooperated to regulate nymphal development for overwintering to achieve seasonal adaptation of the life cycle in M. siamensis.

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Genomic Identification of the TOR Signaling Pathway as a Target of the Plant Alkaloid Antofine in the Phytopathogen Fusarium graminearum

mBio ◽

10.1128/mbio.00792-19 ◽

2019 ◽

Vol 10 (3) ◽

Cited By ~ 1

Author(s):

Christopher Mogg ◽

Christopher Bonner ◽

Li Wang ◽

Johann Schernthaner ◽

Myron Smith ◽

...

Keyword(s):

Signaling Pathway ◽

Fusarium Graminearum ◽

Mode Of Action ◽

Biological Activities ◽

Extensive Study ◽

Economic Losses ◽

Head Blight ◽

Tor Signaling ◽

Content Type ◽

Chemical Genomic

ABSTRACT Antofine, a phenanthroindolizidine alkaloid, is a bioactive natural product isolated from milkweeds that exhibits numerous biological activities, including anticancer, antimicrobial, antiviral, and anti-inflammatory properties. However, the direct targets and mode of action of antofine have not been determined. In this report, we show that antofine displays antifungal properties against the phytopathogen Fusarium graminearum, the cause of Fusarium head blight disease (FHB). FHB does devastating damage to agriculture, causing billions of dollars in economic losses annually. We therefore sought to understand the mode of action of antofine in F. graminearum using insights from yeast chemical genomic screens. We used haploinsufficiency profiling (HIP) to identify putative targets of antofine in yeast and identified three candidate targets, two of which had homologs in F. graminearum. The Fusarium homologues of two targets, glutamate dehydrogenase (FgGDH) and resistance to rapamycin deletion 2 (FgRRD2), can bind antofine. Of the two genes, only the Fgrrd2 knockout displayed a loss of virulence in wheat, indicating that RRD2 is an antivirulence target of antofine in F. graminearum. Mechanistically, we demonstrate that antofine disrupts the interaction between FgRRD2 and FgTap42, which is part of the Tap42-phosphatase complex in the target of rapamycin (TOR) signaling pathway, a central regulator of cell growth in eukaryotes and a pathway of extensive study for controlling numerous pathologies. IMPORTANCE Fusarium head blight caused by the fungal pathogen Fusarium graminearum is a devastating disease of cereal crops worldwide, with limited effective chemical treatments available. Here we show that the natural alkaloid compound antofine can inhibit fusarium head blight in wheat. Using yeast genomic screening, we identified the TOR pathway component RRD2 as a target of antofine that is also required for F. graminearum pathogenicity.

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MRF Family Genes Are Involved in Translation Control, Especially under Energy-Deficient Conditions, and Their Expression and Functions Are Modulated by the TOR Signaling Pathway

The Plant Cell ◽

10.1105/tpc.17.00563 ◽

2017 ◽

Vol 29 (11) ◽

pp. 2895-2920 ◽

Cited By ~ 15

Author(s):

Du-Hwa Lee ◽

Seung Jun Park ◽

Chang Sook Ahn ◽

Hyun-Sook Pai

Keyword(s):

Signaling Pathway ◽

Translation Control ◽

Tor Signaling

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Evaluation of biofloc meal as an ingredient in diets for white shrimp Litopenaeus vannamei under practical conditions: Effect on growth performance, digestive enzymes and TOR signaling pathway

Aquaculture ◽

10.1016/j.aquaculture.2017.06.034 ◽

2017 ◽

Vol 479 ◽

pp. 516-521 ◽

Cited By ~ 22

Author(s):

Jianchun Shao ◽

Mei Liu ◽

Baojie Wang ◽

Keyong Jiang ◽

Mengqiang Wang ◽

...

Keyword(s):

Growth Performance ◽

Signaling Pathway ◽

Litopenaeus Vannamei ◽

Digestive Enzymes ◽

White Shrimp ◽

Tor Signaling ◽

Effect On Growth

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The Target of Rapamycin Signaling Pathway Regulates mRNA Turnover in the YeastSaccharomyces cerevisiae

Molecular Biology of the Cell ◽

10.1091/mbc.12.11.3428 ◽

2001 ◽

Vol 12 (11) ◽

pp. 3428-3438 ◽

Cited By ~ 44

Author(s):

Allan R. Albig ◽

Carolyn J. Decker

Keyword(s):

Signaling Pathway ◽

Mrna Decay ◽

Prolonged Exposure ◽

Specific Inhibitor ◽

Target Of Rapamycin ◽

Mrna Turnover ◽

Diauxic Shift ◽

Nutrient Depletion ◽

Tor Signaling ◽

Tor Pathway

The target of rapamycin (TOR) signaling pathway is an important mechanism by which cell growth is regulated by nutrient availability in eukaryotes. We provide evidence that the TOR signaling pathway controls mRNA turnover in Saccharomyces cerevisiae. During nutrient limitation (diauxic shift) or after treatment with rapamycin (a specific inhibitor of TOR), multiple mRNAs were destabilized, whereas the decay of other mRNAs was unaffected. Our findings suggest that the regulation of mRNA decay by the TOR pathway may play a significant role in controlling gene expression in response to nutrient depletion. The inhibition of the TOR pathway accelerated the major mRNA decay mechanism in yeast, the deadenylation-dependent decapping pathway. Of the destabilized mRNAs, two different responses to rapamycin were observed. Some mRNAs were destabilized rapidly, while others were affected only after prolonged exposure. Our data suggest that the mRNAs that respond rapidly are destabilized because they have short poly(A) tails prematurely either as a result of rapid deadenylation or reduced polyadenylation. In contrast, the mRNAs that respond slowly are destabilized by rapid decapping. In summary, the control of mRNA turnover by the TOR pathway is complex in that it specifically regulates the decay of some mRNAs and not others and that it appears to control decay by multiple mechanisms.

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