Temporal Analysis of the Magnaporthe Oryzae Proteome During Conidial Germination and Cyclic AMP (cAMP)-mediated Appressorium Formation

被引:37
|
作者
Franck, William L. [1 ]
Gokce, Emine [2 ]
Oh, Yeonyee [1 ]
Muddiman, David C. [2 ]
Dean, Ralph A. [1 ]
机构
[1] N Carolina State Univ, Ctr Integrated Fungal Res, Raleigh, NC 27606 USA
[2] N Carolina State Univ, WM Keck Fourier Transform ICR Mass Spectrometry, Dept Chem, Raleigh, NC 27606 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
RICE-BLAST FUNGUS; SACCHAROMYCES-CEREVISIAE; CELL-WALL; RIBOSOMAL-PROTEINS; GENE-EXPRESSION; MOLECULAR CHARACTERIZATION; MELANIN BIOSYNTHESIS; ADENYLATE-CYCLASE; HOST PENETRATION; CHITIN SYNTHASE;
D O I
10.1074/mcp.M112.025874
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Rice blast disease caused by Magnaporthe oryzae is one of the most serious threats to global rice production. During the earliest stages of rice infection, M. oryzae conidia germinate on the leaf surface and form a specialized infection structure termed the appressorium. The development of the appressorium represents the first critical stage of infectious development. A total of 3200 unique proteins were identified by nanoLC-MS/MS in a temporal study of conidial germination and cAMP-induced appressorium formation in M. oryzae. Using spectral counting based label free quantification, observed changes in relative protein abundance during the developmental process revealed changes in the cell wall biosynthetic machinery, transport functions, and production of extracellular proteins in developing appressoria. One hundred and sixty-six up-regulated and 208 down-regulated proteins were identified in response to cAMP treatment. Proteomic analysis of a cAMP-dependent protein kinase A mutant that is compromised in the ability to form appressoria identified proteins whose developmental regulation is dependent on cAMP signaling. Selected reaction monitoring was used for absolute quantification of four regulated proteins to validate the global proteomics data and confirmed the germination or appressorium specific regulation of these proteins. Finally, a comparison of the proteome and transcriptome was performed and revealed little correlation between transcript and protein regulation. A subset of regulated proteins were identified whose transcripts show similar regulation patterns and include many of the most strongly regulated proteins indicating a central role in appressorium formation. A temporal quantitative RT-PCR analysis confirmed a strong correlation between transcript and protein abundance for some but not all genes. Collectively, the data presented here provide the first comprehensive view of the M. oryzae proteome during early infection-related development and highlight biological processes important for pathogenicity.
引用
收藏
页码:2249 / 2265
页数:17
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