E3 Ubiquitin Ligase Regulators of Notch Receptor Endocytosis: From Flies to Humans

Autor: Raluca Revici, Samira Hosseini-Alghaderi, Fabienne Haslam, Rory Whiteford, Martin Baron
Rok vydání: 2021
Předmět:
Zdroj: Revici, R, Hosseini Alghaderi, S S, Haslam, F, Whiteford, R & Baron, M 2022, ' E3 Ubiquitin Ligase Regulators of Notch Receptor Endocytosis: From Flies to Humans ', Biomolecules, vol. 12, no. 2 . https://doi.org/https://www.mdpi.com/2218-273X/12/2/224
Revici, R, Hosseini Alghaderi, S S, Haslam, F, Whiteford, R & Baron, M 2022, ' E3 Ubiquitin Ligase Regulators of Notch Receptor Endocytosis: From Flies to Humans ', Biomolecules, vol. 12, no. 2, 224 . https://doi.org/10.3390/biom12020224, https://doi.org/https://www.mdpi.com/2218-273X/12/2/224
ISSN: 2218-273X
DOI: 10.3390/biom12020224
Popis: Notch is a developmental receptor, conserved in the evolution of the metazoa, which regulates cell fate proliferation and survival in numerous developmental contexts, and also regulates tissue renewal and repair in adult organisms. Notch is activated by proteolytic removal of its extracellular domain and the subsequent release of its intracellular domain, which then acts in the nucleus as part of a transcription factor complex. Numerous regulatory mechanisms exist to tune the amplitude, duration and spatial patterning of this core signalling mechanism. In Drosophila, Deltex (Dx) and Suppressor of dx (Su(dx)) are E3 ubiquitin ligases which interact with the Notch intracellular domain to regulate its endocytic trafficking, with impacts on both ligand-dependent and ligand-independent signal activation. Homologues of Dx and Su(dx) have been shown to also interact with one or more of the four mammalian Notch proteins and other target substrates. Studies have shown similarities, specialisations and diversifications of the roles of these Notch regulators. This review collates together current research on vertebrate Dx and Su(dx)-related proteins, provides an overview of their various roles, and discusses their contributions to cell fate regulation and disease.
Databáze: OpenAIRE