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MaOpy2是一种跨膜蛋白,参与胁迫耐受性和致病性,并通过改变分生孢子形成模式负调控分生孢子产量。

MaOpy2, a Transmembrane Protein, Is Involved in Stress Tolerances and Pathogenicity and Negatively Regulates Conidial Yield by Shifting the Conidiation Pattern in .

作者信息

Wen Zhiqiong, Fan Yu, Xia Yuxian, Jin Kai

机构信息

Genetic Engineering Research Center, School of Life Sciences, Chongqing University, Chongqing 401331, China.

Chongqing Engineering Research Center for Fungal Insecticide, Chongqing 401331, China.

出版信息

J Fungi (Basel). 2022 May 30;8(6):587. doi: 10.3390/jof8060587.

Abstract

Opy2 is an important membrane-anchored protein upstream of the HOG-MAPK signaling pathway and plays important roles in both the HOG-MAPK and Fus3/Kss1 MAPK. In this study, the roles of in were systematically elucidated. The results showed that the disruption significantly reduced fungal tolerances to UV, heat shock and cell-wall-disrupting agents. Bioassays showed that the decreased fungal pathogenicity by topical inoculation mainly resulted from the impaired penetration ability. However, the growth ability of ∆ was enhanced in insect hemolymph. Importantly, deletion could significantly increase the conidial yield of by shifting the conidiation pattern from normal conidiation to microcycle conidiation on the 1/4SDAY medium. Sixty-two differentially expressed genes (DEGs) during the conidiation pattern shift, including 37 up-regulated genes and 25 down-regulated genes in ∆, were identified by RNA-seq. Further analysis revealed that some DEGs were related to conidiation and hyphal development. This study will provide not only the theoretical basis for elucidating the regulation mechanism for improving the conidial yield and quality in but also theoretical guidance for the molecular improvement of entomopathogenic fungi.

摘要

Opy2是HOG-MAPK信号通路上游一种重要的膜锚定蛋白,在HOG-MAPK和Fus3/Kss1 MAPK中均发挥重要作用。在本研究中,系统阐明了其在[具体研究对象]中的作用。结果表明,[具体基因]的破坏显著降低了真菌对紫外线、热休克和细胞壁破坏剂的耐受性。生物测定表明,局部接种导致的真菌致病性降低主要是由于穿透能力受损。然而,在昆虫血淋巴中,∆[具体基因]的生长能力增强。重要的是,通过在1/4SDAY培养基上使产孢模式从正常产孢转变为微循环产孢,[具体基因]的缺失可显著提高[具体真菌]的分生孢子产量。通过RNA-seq鉴定了产孢模式转变过程中的62个差异表达基因(DEG),包括∆[具体基因]中的37个上调基因和25个下调基因。进一步分析表明,一些DEG与产孢和菌丝发育有关。本研究不仅将为阐明提高[具体真菌]分生孢子产量和质量的调控机制提供理论依据,也将为昆虫病原真菌的分子改良提供理论指导。

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