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A molecular recognition feature mediates ribosome-induced SRP-receptor assembly during protein targeting.

Yu-Hsien Hwang FuSowmya ChandrasekarJae Ho LeeShu-Ou Shan
Published in: The Journal of cell biology (2019)
Molecular recognition features (MoRFs) provide interaction motifs in intrinsically disordered protein regions to mediate diverse cellular functions. Here we report that a MoRF element, located in the disordered linker domain of the mammalian signal recognition particle (SRP) receptor and conserved among eukaryotes, plays an essential role in sensing the ribosome during cotranslational protein targeting to the endoplasmic reticulum. Loss of the MoRF in the SRP receptor (SR) largely abolishes the ability of the ribosome to activate SRP-SR assembly and impairs cotranslational protein targeting. These results demonstrate a novel role for MoRF elements and provide a mechanism for the ribosome-induced activation of the mammalian SRP pathway. Kinetic analyses and comparison with the bacterial SRP further suggest that the SR MoRF functionally replaces the essential GNRA tetraloop in the bacterial SRP RNA, providing an example for the replacement of RNA function by proteins during the evolution of ancient ribonucleoprotein particles.
Keyphrases
  • binding protein
  • protein protein
  • endoplasmic reticulum
  • amino acid
  • high glucose
  • diabetic rats
  • oxidative stress
  • transcription factor
  • small molecule
  • drug delivery
  • endothelial cells
  • neural network