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StPBS2是一种促分裂原活化蛋白激酶激酶基因,参与决定玉米大斑病菌丝形态、细胞壁发育、高渗胁迫反应以及次生代谢产物的产生。

StPBS2, a MAPK kinase gene, is involved in determining hyphal morphology, cell wall development, hypertonic stress reaction as well as the production of secondary metabolites in Northern Corn Leaf Blight pathogen Setosphaeria turcica.

作者信息

Gong Xiao-Dong, Feng Sheng-Ze, Zhao Jie, Tang Cong, Tian Lan, Fan Yong-Shan, Cao Zhi-Yan, Hao Zhi-Min, Jia Hui, Zang Jin-Ping, Zhang Yun-Feng, Han Jian-Min, Gu Shou-Qin, Dong Jin-Gao

机构信息

Mycotoxin and Molecular Plant Pathology Laboratory, Hebei Agriculture University, Baoding 071000, PR China.

Mycotoxin and Molecular Plant Pathology Laboratory, Hebei Agriculture University, Baoding 071000, PR China; Department of Life Science, Tangshan Normal University, Tangshan 063000, PR China.

出版信息

Microbiol Res. 2017 Aug;201:30-38. doi: 10.1016/j.micres.2017.04.009. Epub 2017 Apr 26.

Abstract

Mitogen activated protein kinase kinase (MAPKK) is a crucial component in the MAPK signaling pathway. However, the functions of MAPKKs in foliar pathogens remain poorly understood. In the current study, a MAPKK gene designated as StPBS2 was cloned from Setosphaeria turcica and the functions of this gene were investigated by RNAi technology. Four independent StPBS2 gene silence transformants with different efficiencies were confirmed by real time PCR. Compared to the wild type strain (WT), these transformants showed decreased colony growth, shortened hyphae cell length, broadened cell width and an obvious reduction in conidium yield. Moreover, the cell wall of the transformants was thicker and they were also more sensitive to substances that interfere with cell wall biosynthesis than WT. Additionally, the transformants displayed higher sensitivity to hypertonic stress than WT and the sensitivity was associated with the level of silencing of StPBS2. They were also resistant to the fungicides iprodione, procymidone and fludioxonil, to which WT almost completely sensitive. The transformants produced more red secondary metabolites than WT and the production was enhanced with increasing silencing level and increased glucose content in PDA medium. Our results suggest that StPBS2 is involved in morphogenesis, condiogenesis, cell wall development, hypertonic stress reaction and resistance to fungicides, as well as in the biosynthesis of secondary metabolites in S. turcica.

摘要

丝裂原活化蛋白激酶激酶(MAPKK)是MAPK信号通路中的关键组成部分。然而,MAPKKs在叶部病原菌中的功能仍知之甚少。在本研究中,从玉米大斑病菌中克隆了一个名为StPBS2的MAPKK基因,并通过RNAi技术研究了该基因的功能。通过实时PCR确认了四个不同沉默效率的独立StPBS2基因沉默转化体。与野生型菌株(WT)相比,这些转化体的菌落生长减缓,菌丝细胞长度缩短,细胞宽度变宽,分生孢子产量明显降低。此外,转化体的细胞壁更厚,并且它们对干扰细胞壁生物合成的物质比WT更敏感。另外,转化体对高渗胁迫的敏感性高于WT,且敏感性与StPBS2的沉默水平相关。它们对杀菌剂异菌脲、腐霉利和咯菌腈具有抗性,而WT对这些杀菌剂几乎完全敏感。转化体产生的红色次生代谢产物比WT更多,并且随着沉默水平的增加以及PDA培养基中葡萄糖含量的增加,产量提高。我们的结果表明,StPBS2参与了玉米大斑病菌的形态发生、分生孢子形成、细胞壁发育、高渗胁迫反应和对杀菌剂的抗性,以及次生代谢产物的生物合成。

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