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Event: 2268
Key Event Title
Decreased, insulin-induced gene 1 (INSIG1) protein activity
Short name
Biological Context
Level of Biological Organization |
---|
Cellular |
Cell term
Cell term |
---|
eukaryotic cell |
Organ term
Key Event Components
Process | Object | Action |
---|---|---|
decreased circulating total protein level | insulin-induced gene 1 protein | decreased |
Key Event Overview
AOPs Including This Key Event
AOP Name | Role of event in AOP | Point of Contact | Author Status | OECD Status |
---|---|---|---|---|
Activation, Pregnane-X receptor leads to increased plasma LDL cholesterol via synthesis | KeyEvent | John Frisch (send email) | Under development: Not open for comment. Do not cite | |
Activation, Pregnane-X receptor leads to increased plasma LDL cholesterol via PCSK9 | KeyEvent | John Frisch (send email) | Under development: Not open for comment. Do not cite |
Taxonomic Applicability
Term | Scientific Term | Evidence | Link |
---|---|---|---|
mammals | mammals | High | NCBI |
Life Stages
Life stage | Evidence |
---|---|
All life stages | Moderate |
Sex Applicability
Term | Evidence |
---|---|
Unspecific | High |
Key Event Description
Insulin-induced gene 1 (INSIG1) is a transmembrane protein in the endoplasmic reticulum membrane (Ouyang et al. 2020). INSIG1 has an important role in lipid synthesis regulation. At low cholesterol levels, INSIG1 has lower binding affinity for SREBP cleavage-activating protein (SCAP), allowing free SCAP to bind to Coat Protein Complex II (COPII; Ouyang et al. 2020). The SCAP-COPII complex enables Sterol Regulatory Element Binding Proteins (SREBPs) to move through the endoplasmic reticulum to the Golgi, where membrane-bound transcription factor site-1-protease (S1P) and site-2-protease (S2P) enable proteolytic processing that allows SREBPs to enter the nucleus (Yabe et al. 2022; Yang et al. 2022). In the nucleus, SREBP2 increase gene expression for enzymes involved in cholesterol synthesis (Ouyang et al. 2020; Itkonen et al., 2023). At high cholesterol levels, INSIG1 binds to SCAP, competitively inhibiting the ability of SCAP to bind to COPII (Ouyang et al. 2020). SREBPs are retained in the endoplasmic reticulum rather than being transferred to the Golgi, reducing levels of cholesterol synthesis (Ouyang et al. 2020; Itkonen et al., 2023).
How It Is Measured or Detected
Real time PCR can be used to measure INSIG1 transcript abundance, which is an indirect – and only semi-quantitative indicator of INSIG1 protein abundance. INSIG1 protein can be measured via Western blotting or enzyme immunoassay.
Domain of Applicability
Life Stage: All life stages.
Sex: Applies to both males and females.
Taxonomic: Primarily studied in humans and laboratory rodents.
References
Itkonen, A., Hakkola, J., and Rysa, J. 2023. Adverse outcome pathway for pregnane X receptor‑induced hypercholesterolemia. Archives of Toxicology 97: 2861–2877.
Ouyang, S., Mo, Z., Sun, S., Yin, K., and Lv, Y. 2020. Emerging role of Insig-1 in lipid metabolism and lipid disorders. Clinica Chimica Acta 508: 206–212.
Yabe, D., Brown, M.S., and Goldstein, J.L. 2002. Insig-2, a second endoplasmic reticulum protein that binds SCAP and blocks export of sterol regulatory element-binding proteins. Proceedings of the National Academy of Sciences 99(20): 12753–12758.
Yang, T., Espenshade, P.J., Wright, M.E., Yabe, D., Gong, Y., Aebersold, R., Goldstein, J.L., and Brown, M.S. 2002. Crucial step in cholesterol homeostasis: sterols promote binding of SCAP to INSIG-1, a membrane protein that facilitates retention of SREBPs in ER. Cell 110: 489–500.
NOTE: Italics indicate edits from John Frisch October 2024.