Reactome: A Curated Pathway Database

Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling

Stable Identifier
Homo sapiens
Locations in the PathwayBrowser

Loss of function mutations found in FBXW7 in T-cell acute lymphoblastic leukemia are predominantly dominant negative missense mutations that target one of the three highly conserved arginine residues in the WD repeats of FBXW7 (Thompson et al. 2007, O'Neil et al. 2007). These three arginine residues are part of the FBXW7 substrate binding pocket and each one of them contacts the phosphorylated threonine residue in the conserved substrate phosphodegron region (Orlicky et al. 2003). Specifically, FBXW7 interacts with the PEST domain of NOTCH1 upon phosphorylation of the PEST domain by CDK8 (Fryer et al. 2004). FBXW7 mutants are therefore unable to bind and promote ubiquitination of the NOTCH1 intracellular domain (NICD1), leading to prolonged NICD1 transcriptional activity (Thompson et al. 2007, O'Neil et al. 2007).

Literature References
Participant Of
Name Identifier Synonyms
cancer 162 [malignant tumor, malignant neoplasm, primary cancer] malignant tumor, malignant neoplasm, primary cancer