稻瘟病真菌的发育、致病性和自噬都需要二氢烟酸酶MoPyr4。

IF 8.2 2区 生物学 Q1 CELL BIOLOGY
Jing-Yi Wang, Ying-Ying Cai, Lin Li, Xue-Ming Zhu, Zi-Fang Shen, Zi-He Wang, Jian Liao, Jian-Ping Lu, Xiao-Hong Liu, Fu-Cheng Lin
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引用次数: 0

摘要

二氢烟酸酶(DHOase)是内源性嘧啶核苷酸从头生物合成途径六个酶促反应步骤中的第三个酶,该途径在细菌和真核生物中都是保守的代谢途径。然而,有关植物病原真菌中 DHOase 生物功能的研究非常有限。本研究鉴定并命名了稻瘟病真菌 Magnaporthe oryzae 中与酿酒酵母 DHOase Ura4 同源的蛋白 MoPyr4,并研究了其调控真菌生长、致病性和自噬的能力。缺失MoPYR4会导致M. oryzae在生长、分生孢子、附着体形成、糖原和脂滴的转移和降解、附着体张力积累以及侵染性菌丝扩展等方面出现缺陷,最终导致真菌致病性减弱。长期补充外源尿苷-5'-磷酸(UMP)可有效恢复ΔMopyr4突变体的表型和致病性。进一步的研究发现,MoPyr4还参与了Pmk1-MAPK信号通路的调控,与过氧物酶体共定位以进行氧化应激反应,并在高渗应激反应中参与了Osm1-MAPK信号通路的调控。此外,MoPyr4还与参与自噬的核心蛋白MoAtg5相互作用,并对自噬降解进行正向调控。综上所述,我们的研究结果表明,用于 UMP 生物合成的 MoPyr4 对 M. oryzae 的发育和致病性至关重要。我们还发现,MoPyr4 通过参与 Pmk1-MAPK 信号通路、过氧化物酶体相关氧化应激反应机制、Osm1-MAPK 信号通路和自噬通路,在外部应激反应和致病机制中发挥了重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dihydroorotase MoPyr4 is required for development, pathogenicity, and autophagy in rice blast fungus.

Dihydroorotase (DHOase) is the third enzyme in the six enzymatic reaction steps of the endogenous pyrimidine nucleotide de novo biosynthesis pathway, which is a metabolic pathway conserved in both bacteria and eukaryotes. However, research on the biological function of DHOase in plant pathogenic fungi is very limited. In this study, we identified and named MoPyr4, a homologous protein of Saccharomyces cerevisiae DHOase Ura4, in the rice blast fungus Magnaporthe oryzae and investigated its ability to regulate fungal growth, pathogenicity, and autophagy. Deletion of MoPYR4 led to defects in growth, conidiation, appressorium formation, the transfer and degradation of glycogen and lipid droplets, appressorium turgor accumulation, and invasive hypha expansion in M. oryzae, which eventually resulted in weakened fungal pathogenicity. Long-term replenishment of exogenous uridine-5'-phosphate (UMP) can effectively restore the phenotype and virulence of the ΔMopyr4 mutant. Further study revealed that MoPyr4 also participated in the regulation of the Pmk1-MAPK signaling pathway, co-localized with peroxisomes for the oxidative stress response, and was involved in the regulation of the Osm1-MAPK signaling pathway in response to hyperosmotic stress. In addition, MoPyr4 interacted with MoAtg5, the core protein involved in autophagy, and positively regulated autophagic degradation. Taken together, our results suggested that MoPyr4 for UMP biosynthesis was crucial for the development and pathogenicity of M. oryzae. We also revealed that MoPyr4 played an essential role in the external stress response and pathogenic mechanism through participation in the Pmk1-MAPK signaling pathway, peroxisome-related oxidative stress response mechanism, the Osm1-MAPK signaling pathway and the autophagy pathway.

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来源期刊
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
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