Document Detail


Monitoring autophagy in Magnaporthe oryzae.
MedLine Citation:
PMID:  19185727     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
Xiao-Hong Liu; Tong-Bao Liu; Fu-Cheng Lin
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Methods in enzymology     Volume:  451     ISSN:  1557-7988     ISO Abbreviation:  Meth. Enzymol.     Publication Date:  2008  
Date Detail:
Created Date:  2009-02-02     Completed Date:  2009-03-12     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0212271     Medline TA:  Methods Enzymol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  271-94     Citation Subset:  IM    
Affiliation:
State Key Laboratory for Rice Biology, Institute of Biotechnology, Zhejiang University, Huajiachi Campus, Hangzhou, Zhejiang, China.
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MeSH Terms
Descriptor/Qualifier:
Autophagy / genetics,  physiology*
Biological Assay / methods*
Fungal Proteins / genetics,  metabolism*
Genetic Complementation Test
Genetic Vectors / metabolism
Magnaporthe / cytology,  genetics*,  metabolism*,  pathogenicity
Microscopy, Electron / methods
Oryza sativa / microbiology
Phagosomes / metabolism,  ultrastructure
Pichia / genetics,  metabolism
Recombinant Fusion Proteins / genetics,  metabolism
Transcriptional Activation
Chemical
Reg. No./Substance:
0/Fungal Proteins; 0/Recombinant Fusion Proteins

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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