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Rice plasma membrane proteomics reveals Magnaporthe oryzae promotes 2 susceptibility by sequential activation of host hormone signaling pathways
Monday, 2016/11/14 | 07:52:15

 

Jidong Cao, Chao Yang, Lingjuan Li, Lan Jiang, Yao Wu, Chuanwan Wu, Qingyun bu, Guixian Xia, Xiaoyun Liu, Yuanming Luo and Jun Liu

Mol Plant Microbe Interact. 2016 Nov 1. [Epub ahead of print]

ABSTRACT  

 Plant plasma membrane (PM) plays important roles in immune response. Here, we utilized quantitative mass spectrometry to explore the rice PM protein composition 34 and dynamic changes during Magnaporthe oryzae (M. oryzae) infection. We report  thus far the largest rice PM Proteome dataset with 3,906 identified proteins, among which 484 proteins were differentially expressed after M. oryzae infection. One third  of the identified proteins are predicted to have at least one transmembrane domain. Half of the identified proteins are predicted to have binding functions and over one  third of the proteins have enzyme?related functions. In addition, GO analyses revealed that abscisic acid (ABA) and cytokinin (CK) signaling were sequentially activated after M. oryzae infection in rice. We found that the activation of ABA signaling and the suppression of rice immune response occurred at early infection stage, while the activation of CK signaling, the upregulation of sugar transporter genes expression and the nutrient efflux of infected rice cells occurred at later infection stage. Thus, we further propose that M.  oryzae activates ABA signaling to repress rice immune signaling for initial invasion and redirects nutrient efflux of infected cells for massive growth at later infection stage.

 

See https://www.ncbi.nlm.nih.gov/pubmed/27800704

 

Fig. 2.  GO biological  process of differentially expressed proteins  (DEPs). A, DEPs at different time points. The pathogen and  mock-treated  rice  leaves  were  used  for  PM  protein  enrichment.  The  detected  proteins  compared  to  their  respective datasets  with  the  threshold  of  Log2  fold  change  ≥0.5  or  ≤-0.5  were  considered  as  DEPs.  The  number  of  DEPs  are displayed by 24 and 48 hpi, respectively. B, Classification of the DEPs into molecular functions and biological processes. The homology-based annotation was performed by Blast2Go software to analyze the DEPs. The red slices represent the upregulated  proteins,  and  grey  slices  represent  downregulated  proteins.  C,  Heat  map  representing  the  differentially regulated  immune  proteins.  The  DEPs  were  subjected  to  homology-based  annotation   by  Blast2GO  against  RGAP database.

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