Fic-mediated AMPylation tempers the unfolded protein response during physiological stress

Proc Natl Acad Sci U S A. 2022 Aug 9;119(32):e2208317119. doi: 10.1073/pnas.2208317119. Epub 2022 Aug 1.

Abstract

The proper balance of synthesis, folding, modification, and degradation of proteins, also known as protein homeostasis, is vital to cellular health and function. The unfolded protein response (UPR) is activated when the mechanisms maintaining protein homeostasis in the endoplasmic reticulum become overwhelmed. However, prolonged or strong UPR responses can result in elevated inflammation and cellular damage. Previously, we discovered that the enzyme filamentation induced by cyclic-AMP (Fic) can modulate the UPR response via posttranslational modification of binding immunoglobulin protein (BiP) by AMPylation during homeostasis and deAMPylation during stress. Loss of fic in Drosophila leads to vision defects and altered UPR activation in the fly eye. To investigate the importance of Fic-mediated AMPylation in a mammalian system, we generated a conditional null allele of Fic in mice and characterized the effect of Fic loss on the exocrine pancreas. Compared to controls, Fic-/- mice exhibit elevated serum markers for pancreatic dysfunction and display enhanced UPR signaling in the exocrine pancreas in response to physiological and pharmacological stress. In addition, both fic-/- flies and Fic-/- mice show reduced capacity to recover from damage by stress that triggers the UPR. These findings show that Fic-mediated AMPylation acts as a molecular rheostat that is required to temper the UPR response in the mammalian pancreas during physiological stress. Based on these findings, we propose that repeated physiological stress in differentiated tissues requires this rheostat for tissue resilience and continued function over the lifetime of an animal.

Keywords: AMPylation; ER stress; Fic; pancreas; unfolded protein response.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Animals
  • Cyclic AMP* / metabolism
  • Drosophila Proteins* / deficiency
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila melanogaster* / drug effects
  • Drosophila melanogaster* / genetics
  • Drosophila melanogaster* / metabolism
  • Endoplasmic Reticulum / drug effects
  • Endoplasmic Reticulum / metabolism
  • Endoplasmic Reticulum Stress* / drug effects
  • Mice
  • Nucleotidyltransferases* / deficiency
  • Nucleotidyltransferases* / genetics
  • Nucleotidyltransferases* / metabolism
  • Pancreas / drug effects
  • Pancreas / enzymology
  • Pancreas / metabolism
  • Pancreas / physiopathology
  • Stress, Physiological* / drug effects
  • Unfolded Protein Response* / drug effects

Substances

  • Cyclic AMP
  • Drosophila Proteins
  • Fic protein, Drosophila
  • Nucleotidyltransferases
  • ficd protein, mouse