HuR (ELAVL1) binds and stabilizes mRNA

Summary
Organism
Homo sapiens (human)
Reactome
R-HSA-450520
PubChem
R-HSA-450520
Description
  • HuR (ELAVL1) is a ubiquitous protein that binds AU-rich elements in mRNAs and acts to stabilize the mRNAs. HuR activity is controlled by phosphorylation, with PKC alpha and PCK delta enhancing the ability of HuR to bind and stabilize mRNAs. Binding of mRNAs occurs in the nucleus and HuR then interacts with the CRM1 export pathway to transfer the mRNA to the cytoplasm. The mechanism by which HuR shields the mRNA from degradation is unknown.
    HuR also regulates translation of some mRNAs, in some cases repressing translation and in some cases enhancing translation of bound mRNAs by recruiting them to polysomes.
    HuR binds and regulates mRNAs encoding Cyclooxygenase-2 (COX2, PTGS2), Cyclin A (CCNA, CCNA2), Cyclin D1 (CCND1), Cyclin B1 (CCNB1), CD83 antigen (CD83), and proto-oncogene c-Fos (FOS).
    HuR is a member of a family of proteins that also contains HuD (ELAVL4), HuB (ELAVL2), and HuC (ELAVL3). HuB, HuC, and HuD are specifically expressed in neural tissue.
    HuR participates in apoptosis. During lethal stress HuR becomes mostly cytoplasmic and is a target of Caspase-3 and Caspase-7. The cleavage products of HuR in turn promote apoptosis.
Click on a node on the pathway to see its details. Glycoproteins are marked with a glycoprotein icon in their name.
Displaying all 6 entries
UniProt ID Protein Name Gene Symbol Pathway Viewer
O14980 Exportin-1
  • CRM1
  • XPO1
view
O75888 Tumor necrosis factor ligand superfamily member 13
  • APRIL
  • TALL2
  • TNFSF13
  • UNQ383/PRO715
  • ZTNF2
view
P17252 Protein kinase C alpha type
  • PKCA
  • PRKACA
  • PRKCA
view
P35658 Nuclear pore complex protein Nup214
  • CAIN
  • CAN
  • KIAA0023
  • NUP214
view
Q01105 Protein SET
  • SET
view
Q15717 ELAV-like protein 1
  • ELAVL1
  • HUR
view

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026