Nuclear pore permeabilization is a convergent signaling event in effector-triggered immunity

• Yangnan Gu ^[1] ; Sophia G. Zebell ^[1] ; Zizhen Liang ^[2]
  1. [1] Duke University

     Duke University

     Township of Durham, Estados Unidos

     
  2. [2] Chinese University of Hong Kong

     Chinese University of Hong Kong

     RAE de Hong Kong (China)

     
• Localización: Cell, ISSN 0092-8674, Vol. 166, Nº. 6, 2016, págs. 1526-1538
• Idioma: inglés
• Texto completo no disponible (Saber más ...)
• Resumen

  • Nuclear transport of immune receptors, signal transducers, and transcription factors is an essential regulatory mechanism for immune activation. Whether and how this process is regulated at the level of the nuclear pore complex (NPC) remains unclear. Here, we report that CPR5, which plays a key inhibitory role in effector-triggered immunity (ETI) and programmed cell death (PCD) in plants, is a novel transmembrane nucleoporin. CPR5 associates with anchors of the NPC selective barrier to constrain nuclear access of signaling cargos and sequesters cyclin-dependent kinase inhibitors (CKIs) involved in ETI signal transduction. Upon activation by immunoreceptors, CPR5 undergoes an oligomer to monomer conformational switch, which coordinates CKI release for ETI signaling and reconfigures the selective barrier to allow significant influx of nuclear signaling cargos through the NPC. Consequently, these coordinated NPC actions result in simultaneous activation of diverse stress-related signaling pathways and constitute an essential regulatory mechanism specific for ETI/PCD induction.