4.7 Article

Modulation of RNA Polymerase II Phosphorylation Downstream of Pathogen Perception Orchestrates Plant Immunity

期刊

CELL HOST & MICROBE
卷 16, 期 6, 页码 748-758

出版社

CELL PRESS
DOI: 10.1016/j.chom.2014.10.018

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资金

  1. NIH [R01GM092893, R01GM097247]
  2. NSF [IOS-1252539, MCB-0950459]
  3. Robert A. Welch Foundation [A-1795]
  4. Texas AgriLife Genomics Seed Grant
  5. China Scholarship Council
  6. Rio de Janeiro State Research Foundation (FAPERJ), Brazil
  7. NSF REU program
  8. Direct For Biological Sciences
  9. Div Of Biological Infrastructure [1358941] Funding Source: National Science Foundation
  10. Division Of Integrative Organismal Systems
  11. Direct For Biological Sciences [1252539, 1146589] Funding Source: National Science Foundation
  12. Div Of Molecular and Cellular Bioscience
  13. Direct For Biological Sciences [0950459] Funding Source: National Science Foundation

向作者/读者索取更多资源

Perception of microbe-associated molecular patterns (MAMPs) elicits host transcriptional reprogramming as part of the immune response. Although pathogen perception is well studied, the signaling networks orchestrating immune gene expression remain less clear. In a genetic screen for components involved in the early immune gene transcription reprogramming, we identified Arabidopsis RNA polymerase II C-terminal domain (CTD) phosphatase-like 3 (CPL3) as a negative regulator of immune gene expression. MAMP perception induced rapid and transient cyclin-dependent kinase C (CDKC)-mediated phosphorylation of Arabidopsis CTD. The CDKCs, which are in turn phosphorylated and activated by a canonical MAP kinase (MAPK) cascade, represent a point of signaling convergence downstream of multiple immune receptors. CPL3 directly dephos-phorylated CTD to counteract MAPK-mediated CDKC regulation. Thus, modulation of the phosphorylation dynamics of eukaryotic RNA polymerase II transcription machinery by MAPKs, CTD kinases, and phosphatases constitutes an essential mechanism for rapid orchestration of host immune gene expression and defense upon pathogen attacks.

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