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监测稻瘟病菌中的自噬作用。

Monitoring autophagy in Magnaporthe oryzae.

作者信息

Liu Xiao-Hong, Liu Tong-Bao, Lin Fu-Cheng

机构信息

State Key Laboratory for Rice Biology, Institute of Biotechnology, Zhejiang University, Huajiachi Campus, Hangzhou, Zhejiang, China.

出版信息

Methods Enzymol. 2008;451:271-94. doi: 10.1016/S0076-6879(08)03219-9.

Abstract

Autophagy is a ubiquitous degradative pathway for the bulk degradation of eukaryotic macromolecules and organelles in eukaryotic cells (Klionsky, 2005; Levine and Klionsky, 2004). Previously, the role of autophagy in turgor generation in plant pathogenic fungi was unknown. Currently, autophagy is confirmed as an important pathway for turgor accumulation in the appressorium (the tips of the invasive hyphae; Liu et al., 2007b) using a technique of targeted gene replacement, deleting the genes that code for Magnaporthe oryzae homologs of yeast autophagy-related (ATG) genes ATG2, ATG4, ATG5, ATG8, ATG9, and ATG18 (Liu et al., 2007a). All of these null mutants fail to breach the cuticle of the host. This chapter will first look at some methodologies to analyze the functions of autophagy-related gene products at the biological, cellular, and molecular level in this model plant pathogenic fungi, and then provide some research evidence of the role of autophagy in the promotion of the formation of the infection structure and pathogenicity to point out some significant areas for further research in this field.

摘要

自噬是真核细胞中用于大量降解真核生物大分子和细胞器的普遍存在的降解途径(克利昂斯基,2005年;莱文和克利昂斯基,2004年)。以前,自噬在植物病原真菌膨压产生中的作用尚不清楚。目前,利用靶向基因替换技术,删除编码稻瘟病菌酵母自噬相关(ATG)基因ATG2、ATG4、ATG5、ATG8、ATG9和ATG18同源物的基因,自噬被确认为附着胞(侵入菌丝的尖端)中膨压积累的重要途径(刘等人,2007b)。所有这些缺失突变体都无法突破宿主的角质层。本章将首先探讨一些在这种模式植物病原真菌中,在生物学、细胞和分子水平上分析自噬相关基因产物功能的方法,然后提供一些关于自噬在促进感染结构形成和致病性方面作用的研究证据,以指出该领域进一步研究的一些重要方向。

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