例如:"lncRNA", "apoptosis", "WRKY"

PKR-dependent cytosolic cGAS foci are necessary for intracellular DNA sensing.

Sci Signal. 2019 Nov 26;12(609)
Siqi Hu 1 , Hong Sun 1 , Lijuan Yin 1 , Jian Li 1 , Shan Mei 1 , Fengwen Xu 1 , Chao Wu 2 , Xiaoman Liu 1 , Fei Zhao 1 , Di Zhang 1 , Yu Huang 1 , Lili Ren 2 , Shan Cen 3 , Jianwei Wang 4 , Chen Liang 5 , Fei Guo 6
Siqi Hu 1 , Hong Sun 1 , Lijuan Yin 1 , Jian Li 1 , Shan Mei 1 , Fengwen Xu 1 , Chao Wu 2 , Xiaoman Liu 1 , Fei Zhao 1 , Di Zhang 1 , Yu Huang 1 , Lili Ren 2 , Shan Cen 3 , Jianwei Wang 4 , Chen Liang 5 , Fei Guo 6
+ et al

[No authors listed]

Author information
  • 1 NHC Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology and Center for AIDS Research, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, P. R. China.
  • 2 NHC Key Laboratory of Systems Biology of Pathogens and Christophe Mérieux Laboratory, IPB-Fondation Mérieux, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, P. R. China.
  • 3 Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100005, P. R. China.
  • 4 NHC Key Laboratory of Systems Biology of Pathogens and Christophe Mérieux Laboratory, IPB-Fondation Mérieux, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, P. R. China. guofei@ipb.pumc.edu.cn chen.liang@mcgill.ca wangjw28@163.com.
  • 5 McGill University AIDS Centre, Lady Davis Institute, Jewish General Hospital, Montreal H3T 1E2, Canada. guofei@ipb.pumc.edu.cn chen.liang@mcgill.ca wangjw28@163.com.
  • 6 NHC Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology and Center for AIDS Research, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, P. R. China. guofei@ipb.pumc.edu.cn chen.liang@mcgill.ca wangjw28@163.com.

摘要


Cyclic GMP-AMP synthase (cGAS) is a major sensor of cytosolic DNA from invading pathogens and damaged cellular organelles. Activation of cGAS promotes liquid-like phase separation and formation of membraneless cytoplasmic structures. Here, we found that cGAS bound G3BP1, a double-stranded nucleic acid helicase involved in the formation of stress granules. Loss of G3BP1 blocked subcellular cGAS condensation and suppressed the interferon response to intracellular DNA and DNA virus particles in cells. Furthermore, an RNA-dependent association with PKR promoted G3BP1 foci formation and cGAS-dependent interferon responses. Together, these results indicate that PKR promotes the formation of G3BP1-dependent, membraneless cytoplasmic structures necessary for the DNA-sensing function of cGAS in human cells. These data suggest that there is a previously unappreciated link between nucleic acid sensing pathways, which requires the formation of specialized subcellular structures.