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Rho2 参与了腐皮镰刀菌的发育、应激反应和致病性。

Rho2 involved in development, stress response and pathogenicity of Fusarium oxysporum.

机构信息

Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, 650500, China.

Key Laboratory of Panax notoginseng Resources Sustainable Development and Utilization of State Administration of Traditional Chinese Medicine, Kunming, 650500, China.

出版信息

World J Microbiol Biotechnol. 2023 Aug 7;39(10):272. doi: 10.1007/s11274-023-03720-2.

Abstract

Rho GTPases regulate the activity of cell wall biosynthesis, actin assembly and polar cell secretion. However, the function of Rho GTPase in filamentous fungi is poorly understood. To understand the role of Rho2 GTPase in Fusarium oxysporum, which is one of root rot pathogens of Panax notoginseng, △rho2 mutant was constructed. Phenotypes of △rho2, including conidiation, germination of spores, stresses (osmotic-, cell membrane-, cell wall disturbing-, metal-, and high temperature-) tolerance and pathogenicity were analyzed. The results showed that the growth of △rho2 was destroyed under cell wall disturbing stress and high temperature stress, suggesting that Rho2 regulated the response of F. oxysporum to cell wall synthesis inhibitors and high temperature stress. Germination of spores and pathogenicity to P. notoginseng were reduced in △rho2 mutant. Western blot results showed that rho2 deletion increased the phosphorylation level of Mpk1. To identify genes regulated by Rho2, transcriptome sequencing was carried out. 2477 genes were identified as upregulated genes and 2177 genes were identified as downregulated genes after rho2 was deleted. These genes provide clues for further study of rho2 function.

摘要

Rho GTPases 调节细胞壁生物合成、肌动蛋白组装和极性细胞分泌的活性。然而,Rho GTPase 在丝状真菌中的功能知之甚少。为了了解 Rho2 GTPase 在根腐病病原菌之一的西洋参腐烂病菌中的作用,构建了 △rho2 突变体。分析了 △rho2 的表型,包括分生孢子形成、孢子萌发、应激(渗透、细胞膜、细胞壁干扰、金属和高温)耐受和致病性。结果表明,在细胞壁干扰应激和高温应激下,△rho2 的生长被破坏,表明 Rho2 调节了 F. oxysporum 对细胞壁合成抑制剂和高温应激的反应。孢子萌发和对西洋参的致病性在 △rho2 突变体中降低。Western blot 结果表明,rho2 缺失增加了 Mpk1 的磷酸化水平。为了鉴定由 Rho2 调控的基因,进行了转录组测序。rho2 缺失后,鉴定出 2477 个上调基因和 2177 个下调基因。这些基因为进一步研究 rho2 功能提供了线索。

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