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  • Shedding light on autophagy coordinating with cell wall integrity signaling to govern pathogenicity of Magnaporthe oryzae.

Shedding light on autophagy coordinating with cell wall integrity signaling to govern pathogenicity of Magnaporthe oryzae.

Autophagy (2019-07-18)
Ziyi Yin, Wanzhen Feng, Chen Chen, Jiayun Xu, Ying Li, Lina Yang, Jingzhen Wang, Xinyu Liu, Wenhao Wang, Chuyun Gao, Haifeng Zhang, Xiaobo Zheng, Ping Wang, Zhengguang Zhang
要旨

Cells are faced with various stresses during their growth and development, and autophagy is a degradative process in which cells can break down their own components to recycle macromolecules and provide energy under these stresses. For pathogenic fungi that utilize cell wall as the first barrier against external stress, the cell wall integrity (CWI) pathway also provides an essential role in responding to these stresses. However, the specific connection between autophagy and CWI remains elusive in either the model fungi including budding yeast Saccharomyces cerevisiae or the rice blast fungus Magnaporthe oryzae. Here, we provided evidence that the endoplasmic reticulum (ER) stress is highly induced during M. oryzae infection and that CWI MAP kinase kinase MoMkk1 (S. cerevisiae Mkk1/2 homolog) was subject to phosphorylation regulation by MoAtg1, the only identified kinase in the core autophagy machinery. We also identified MoMkk1 serine 115 as the MoAtg1-dependent phosphorylation site and this phosphorylation could activate CWI, similar to that by the conserved MAP kinase kinase kinase MoMck1 (S. cerevisiae Bck1 homolog). Together with the first report of MoMkk1 subjects to phosphorylation regulation by MoAtg1, we revealed a new mechanism by which autophagy coordinates with CWI signaling under ER stress, and this MoAtg1-dependent MoMkk1 phosphorylation is essential for the pathogenicity of M. oryzae.Abbreviations: A/Ala: alanine; Atg: autophagy-related; Bck1: bypass of C kinase 1; co-IP: co-immunoprecipitation; CWI: cell wall integrity;DTT: dithiothreitol; ER: endoplasmic reticulum; GFP: green fluorescent protein; Mo: Magnaporthe oryzae; MAPK: mitogen-activated protein kinase; Mkk1: mitogen-activated protein kinase-kinase 1; MS: mass spectrometry; PAS: phagophore assembly site; RFP: red fluorescent protein; RT: room temperature; S/Ser: serine; Slt2: suppressor of the lytic phenotype 2; T/Thr: threonine; UPR: unfolded protein response; Y2H: yeast two-hybrid screen.

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リン酸ナトリウム 一塩基性 一水和物, ACS reagent, ≥98%
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リン酸ナトリウム 二塩基性 七水和物, ACS reagent, 98.0-102.0%
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Triton X-100, for molecular biology
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ヨードアセトアミド, BioUltra
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L-アスコルビン酸, BioXtra, ≥99.0%, crystalline
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リン酸ナトリウム 二塩基性 二水和物, BioUltra, for molecular biology, ≥99.0% (T)
Millipore
Miracloth, Rapid, effective filtration of homogenates
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ギ酸, ACS reagent, ≥88%
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チアミン 塩酸塩, BioReagent, suitable for cell culture, suitable for insect cell culture, suitable for plant cell culture
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リン酸ナトリウム, 一塩基酸 二水和物, BioUltra, for molecular biology, ≥99.0% (T)
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リン酸ナトリウム 二塩基性 十二水和物, BioXtra, ≥99.0% (T)
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ピリドキシン, ≥98%
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BL21(DE3)化学的コンピテントセル, for protein expression
Millipore
Immobilon®-PSQ PVDFメンブレン, 1 roll, 27 cm x 3.75 m, 0.2 µm pore size, Hydrophobic PVDF Transfer Membrane for western blotting.
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アセトニトリル, anhydrous, 99.8%
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アデノシン 5′-三リン酸(ATP) 二ナトリウム塩 水和物, vial of ~1 mg ATP
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四酸化オスミウム, ACS reagent, ≥98.0%
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IGEPAL® CA-630, viscous liquid
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α-キモトリプシン ウシ膵臓由来, suitable for protein sequencing, salt-free, lyophilized powder
Supelco
ドデセニルコハク酸無水物, for microscopy