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Enhanced sensitivity to DSS colitis caused by a hypomorphic Mbtps1 mutation disrupting the ATF6-driven unfolded protein response.

Here, we describe an N-ethyl-N-nitrosourea (ENU)-induced missense error in the membrane-bound transcription factor peptidase site 1 (S1P)-encoding gene (Mbtps1) that causes enhanced susceptibility to dextran sodium sulfate (DSS)-induced colitis. S1P cleaves and activates cAMP response element binding protein/ATF transcription factors, the sterol regulatory element-binding proteins (SREBPs), and other proteins of both endogenous and viral origin. Because S1P has a nonredundant function in the ATF6-dependent unfolded protein response (UPR), woodrat mice show diminished levels of major endoplasmic reticulum chaperones GRP78 (BiP) and GRP94 in the colon upon DSS administration. Experiments with bone marrow chimeric mice reveal a requirement for S1P in nonhematopoietic cells, without which a diminished UPR and colitis develop.

Pubmed ID: 19202076

Authors

  • Brandl K
  • Rutschmann S
  • Li X
  • Du X
  • Xiao N
  • Schnabl B
  • Brenner DA
  • Beutler B

Journal

Proceedings of the National Academy of Sciences of the United States of America

Publication Data

March 3, 2009

Associated Grants

None

Mesh Terms

  • Activating Transcription Factor 6
  • Animals
  • Colitis
  • Dextran Sulfate
  • Endoplasmic Reticulum
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Mutation
  • Proprotein Convertases
  • Protein Folding
  • Serine Endopeptidases
  • Substrate Specificity